1. Cell Biology

Metabolic flexibility via mitochondrial BCAA carrier SLC25A44 is required for optimal fever

  1. Takeshi Yoneshiro
  2. Naoya Kataoka
  3. Jacquelyn M Walejko
  4. Kenji Ikeda
  5. Zachary Brown
  6. Momoko Yoneshiro
  7. Scott B Crown
  8. Tsuyoshi Osawa
  9. Juro Sakai
  10. Robert W McGarrah
  11. Phillip J White
  12. Kazuhiro Nakamura
  13. Shingo Kajimura  Is a corresponding author
  1. Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, United States
  2. Division of Metabolic Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Japan
  3. Department of Integrative Physiology, Nagoya University Graduate School of Medicine, Japan
  4. Duke Molecular Physiology Institute, Duke University School of Medicine, United States
  5. Department of Molecular Endocrinology and Metabolism, Tokyo Medical and Dental University, Japan
  6. Division of Integrative Nutriomics and Oncology, Research Center for Advanced Science and Technology, The University of Tokyo, Japan
  7. Division of Molecular Physiology and Metabolism, Tohoku University Graduate School of Medicine, Japan
  8. Department of Medicine, Division of Cardiology, Duke University School of Medicine, United States
  9. Department of Medicine, Division of EndocrinologyMetabolism and Nutrition, Duke University School of Medicine, United States
  10. Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, United States
https://doi.org/10.7554/eLife.66865
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Cite this article
  1. Takeshi Yoneshiro
  2. Naoya Kataoka
  3. Jacquelyn M Walejko
  4. Kenji Ikeda
  5. Zachary Brown
  6. Momoko Yoneshiro
  7. Scott B Crown
  8. Tsuyoshi Osawa
  9. Juro Sakai
  10. Robert W McGarrah
  11. Phillip J White
  12. Kazuhiro Nakamura
  13. Shingo Kajimura
(2021)
Metabolic flexibility via mitochondrial BCAA carrier SLC25A44 is required for optimal fever
eLife 10:e66865.
https://doi.org/10.7554/eLife.66865
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Abstract

Importing necessary metabolites into the mitochondrial matrix is a crucial step of fuel choice during stress adaptation. Branched chain-amino acids (BCAAs) are essential amino acids needed for anabolic processes, but they are also imported into the mitochondria for catabolic reactions. What controls the distinct subcellular BCAA utilization during stress adaptation is insufficiently understood. The present study reports the role of SLC25A44, a recently identified mitochondrial BCAA carrier (MBC), in the regulation of mitochondrial BCAA catabolism and adaptive response to fever in rodents. We found that mitochondrial BCAA oxidation in brown adipose tissue (BAT) is significantly enhanced during fever in response to the pyrogenic mediator prostaglandin E2 (PGE2) and psychological stress in mice and rats. Genetic deletion of MBC in a BAT-specific manner blunts mitochondrial BCAA oxidation and non-shivering thermogenesis following intracerebroventricular PGE2 administration. At a cellular level, MBC is required for mitochondrial BCAA deamination as well as the synthesis of mitochondrial amino acids and TCA intermediates. Together, these results illuminate the role of MBC as a determinant of metabolic flexibility to mitochondrial BCAA catabolism and optimal febrile responses. This study also offers an opportunity to control fever by rewiring the subcellular BCAA fate.

Introduction

Eukaryotic cells utilize metabolites in distinct organelles during adaptation to stress. Such adaptive mechanisms provide another layer of flexibility in metabolite utilization, a.k.a., metabolic flexibility, thereby allowing for robust adaptive fitness to stress. For example, leucine is a branched-chain amino acid (BCAA) that is essential amino acid needed for anabolic processes, including protein synthesis and nutrition sensing via mTOR activation; however, leucine is also imported into the mitochondrial matrix for catabolic processes in metabolic organs, such as skeletal muscle and brown adipose tissue (BAT) upon exercise and cold adaptation, respectively (Neinast et al., 2019a; Lynch and Adams, 2014). The factors controlling the subcellular metabolite utilization, for example, the anabolic vs. catabolic responses to BCAA, during stress adaptation remain poorly understood.

One of the key determinants for subcellular metabolite utilization is mitochondrial carrier proteins. Relative to the outer membrane, the mitochondrial inner membrane is highly impermeable to molecules and ions, and thus, a variety of carrier proteins in the mitochondrial inner membrane play pivotal roles in the regulation of metabolite delivery into the mitochondrial matrix. For instance, mitochondrial pyruvate carrier proteins (MPC1 and MPC2) are responsible for importing pyruvate into the matrix (Bricker et al., 2012; Herzig et al., 2012). Loss of MPC leads to reduced pyruvate oxidation, thereby shifting cellular metabolism toward glycolysis, a.k.a., the Warburg effect, whereas ectopic expression of MPC1/2 promotes mitochondrial pyruvate oxidation via pyruvate dehydrogenase (PDH) (Schell et al., 2014; Vacanti et al., 2014). Of note, mitochondrial pyruvate uptake via MPC is essential for optimal adaptation to cold environment because genetic loss of MPC1 reduces glucose oxidation and TCA intermediates in brown adipocytes, leading to impaired BAT thermogenesis and cold tolerance in mice (Panic et al., 2020).

We recently identified SLC25A44 as a mitochondrial BCAA carrier (MBC) that is required for mitochondrial BCAA import and subsequent oxidation of BCAA in the matrix (Yoneshiro et al., 2019). CRISPRi-mediated depletion of Slc25a44 decreases mitochondrial BCAA oxidation, thereby attenuating systemic BCAA clearance and cold tolerance in mice (Yoneshiro et al., 2019). A limitation of the previous study, however, is that MBC is widely expressed in the brain, skeletal muscle, and BAT, and thus, the tissue-specific contribution of MBC remains unknown. Accordingly, the present study generated the BAT-specific MBC knock-out (KO) mice and rigorously determined the extent to which mitochondrial BCAA catabolism via MBC is required for thermogenesis and metabolic adaptation to fever.

Fever is a physiological response to pyrogens, and in general, associated with a survival benefit. However, prolonged thermogenesis that chronically exceeds heat loss, such as psychological stress-induced hyperthermia, malignant hyperthermia, brain injury-induced fever, and endocrine fever, is deleterious and can cause widespread damage at cellular and organismal levels (Walter et al., 2016; Evans et al., 2015). Although recent studies uncovered the central neural circuits that control fever in response to pyrogens and psychological stress (Morrison and Nakamura, 2019), cellular and molecular mechanisms of febrile responses in peripheral organs are insufficiently understood. Hence, better understandings of the fever-associated metabolic adaptation may offer an effective intervention to soothe persistent fever.

Here, we report that mitochondrial BCAA oxidation in BAT is significantly enhanced during fever triggered by prostaglandin E2 (PGE2) and psychological stress. Mitochondrial BCAA uptake via MBC is crucial for cellular metabolic flexibility to catabolize BCAA in the mitochondria: BAT-specific MBC loss blunts mitochondrial BCAA catabolism and PGE2-induced fever in mice. Mechanistically, mitochondrial BCAA uptake via MBC is crucial for the synthesis of mitochondrial amino acids and TCA intermediates. Together, the present study provides new insights into the molecular mechanism by which mitochondrial BCAA transport via MBC regulates metabolic flexibility to BCAA catabolism and adaptive fitness to fever.

Results

Fever promotes BCAA oxidation in BAT

We developed an in vivo monitoring system that allowed us to simultaneously record temperature changes in the body core and peripheral tissues of mice in response to thermogenic stimuli (Figure 1A, B). As a stimulus of fever, we used intracerebroventricular (ICV) administration of PGE2. PGE2 is a well-established pyrogenic mediator that binds to the EP3 subtype of its receptor in the preoptic area (POA) and triggers the pyrogenic circuit mechanism for the stimulation of sympathetic nerve activity likely by inhibiting thermoregulatory warm-sensitive POA neurons (Nakamura and Morrison, 2011; Nakamura, 2011). An ICV administration of PGE2 into the POA sufficiently stimulates the non-shivering thermogenesis in BAT without altering the afferent signaling to the POA in rats (Nakamura et al., 2002; Nakamura and Morrison, 2008). Indicating the importance of the PGE2-mediated signaling in infection-induced fever, EP3 receptor KO mice fail to develop fever in response to intraperitoneal (i.p.) injection of lipopolysaccharide (LPS), an experimental model of systemic bacterial infection (Ushikubi et al., 1998; Lazarus et al., 2007).

Figure 1
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Activation of branched chain-amino acid (BCAA) catabolism and thermogenesis in the brown adipose tissue (BAT) following fever stimuli.

(A) The injection site of prostaglandin E2 (PGE2) in the left lateral ventricle. The image was adapted from ‘The mouse brain in stereotaxic coordinates’ (Franklin and Paxinos, 2008). (B) Schematic illustration of the experiment. Mice received intracerebroventricular (ICV) administration of PGE2 (1.4 μg/mouse) or saline (control). Tissue temperature and rectal temperature were simultaneously recorded by the live monitoring system. (C) Real-time temperature changes in the interscapular BAT (iBAT) and rectum of mice in (B). n = 6 per group. (D) Immunoblotting of UCP1 in BAT of mice in (C). BAT was harvested after 2 hr of an ICV administration of PGE2. β-Actin was used as a loading control. n = 3 for saline, n = 4 for PGE2. (E) Plasma BCAA concentration before and after an ICV administration of PGE2. Plasma samples were harvested after 2 hr of an ICV administration of PGE2. n = 6 per group. (F) Relative [1-14C] Val oxidation in isolated iBAT of mice. The iBAT tissues of mice were dissected after 2 hr of an ICV administration of PGE2. n = 4 per group. (G) Relative [1-14C] Val oxidation in isolated iBAT of rats exposed to social defeat stress. The iBAT of rats was dissected 2 hr after social defeat stress. n = 5 per group. *p<0.05, **p<0.01, n.s., not significant. Data were analyzed by using paired t-test (E) or unpaired Student’s t-test (F, G).

Figure 1—source data 1

Activation of branched chain-amino acid (BCAA) catabolism and thermogenesis in the brown adipose tissue (BAT) following fever stimuli.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig1-data1-v2.xlsx

Consistent with previous results (Nakamura et al., 2002), an ICV administration of PGE2 (1.4 μg/mouse) rapidly increased the interscapular BAT (iBAT) temperature within 1–2 min following the administration (Figure 1C), whereas it did not change the protein expression of UCP1 in the iBAT (Figure 1D). This elevation of iBAT temperature was seen selectively to PGE2 but not due to the technical artifact of ICV injection because iBAT temperature was not increased by an ICV administration of saline. The increase in iBAT temperature was followed by a significant increase in core body (rectal) temperature by approximately 2°C (average core body temperature rose to 38.8°C) with a delay of 1–2 min, suggesting that the iBAT is a major heat source for the development of PGE2-induced fever. Of note, chronic treatment with PGE2 analog or ectopic expression of cyclooxygenase (COX) 2, a rate-limiting enzyme in prostaglandin synthesis, promotes beige fat biogenesis in the inguinal WAT (Vegiopoulos et al., 2010; Madsen et al., 2010). In contrast, the present study employed central administration of PGE2 to acutely provoke febrile responses, and thus, PGE2-induced browning of WAT was negligible in this context unless mice were acclimated to cold prior to PGE2 administration (see Figure 2). Following the PGE2-induced febrile response, plasma levels of BCAA were significantly reduced, whereas no significant change was seen after saline administration (Figure 1E). Importantly, this reduction in plasma BCAA levels was accompanied by a significant increase in Val oxidation in the isolated BAT (Figure 1F). This observation is consistent with our previous finding that cold-induced thermogenesis stimulates BCAA uptake in BAT and systemic BCAA clearance (Yoneshiro et al., 2019).

Figure 2
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Mitochondrial branched chain-amino acid (BCAA) catabolism enhances prostaglandin E2 (PGE2)-induced fever.

(A) mRNA expression of indicated BCAA catabolism genes and thermogenic genes in brown adipose tissue (BAT) following cold exposure. n = 3 per group. Data were obtained from a previous microarray dataset from GEO under the accession # GSE51080 (Rosell et al., 2014). (B) mRNA expression of indicated BCAA catabolism genes and thermogenic genes in BAT following β3-AR agonist (CL-316243; CL) treatment. n = 3 per group. Data were obtained from a previous RNA-sequence dataset from ArrayExpress under the accession # E-MTAB-7445 (Tajima et al., 2019). (C) Real-time temperature changes in the interscapular BAT (iBAT) (ΔTBAT), rectum (ΔTRec), and ing-WAT (ΔTIng) of mice acclimated to thermoneutrality (TN, 30°C) or cold (15°C) for 2 weeks. n = 5 per group. (D) Real-time temperature changes in the iBAT (ΔTBAT), rectum (ΔTRec), and ing-WAT (ΔTIng) of mice treated with β3-AR agonist (CL-316243; CL) for 1 week. Saline, n = 4; CL, n = 5. (E) PGE2-stimulated total heat production, maximal temperature (TMax), and velocity of tissue temperature in the iBAT of mice in (C) and (D). Data were analyzed by using unpaired Student’s t-test (A, B, E) or two-way repeated measures ANOVA (C, D).

Figure 2—source data 1

Mitochondrial branched chain-amino acid (BCAA) catabolism enhances prostaglandin E2 (PGE2-)-induced fever.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig2-data1-v2.xlsx

It is worth noting that the increase in BCAA oxidation in BAT is not specific to ICV administration of PGE2 into mice. Psychological stress-induced hyperthermia is another physiological febrile response in which social defeat stress stimulates excitatory neurotransmission from a ventromedial prefrontal cortical site to the dorsomedial hypothalamus, leading to activation of BAT thermogenesis and stress-induced hyperthermia in rats (Kataoka et al., 2020). The role of BAT thermogenesis in psychological stress has also been reported in humans (Robinson et al., 2016). Following social defeat stress in rats, we observed a significant increase in BCAA oxidation in the isolated BAT of rats under stress (Figure 1G). These results suggest that BCAA oxidation and thermogenesis in the BAT are augmented during the development of fever triggered by PGE2 and psychological stress.

Mitochondrial BCAA catabolism enhances PGE2-induced fever

Cold exposure and the subsequent activation of β3-adrenoceptor (AR) signaling potently stimulates BAT thermogenesis (Collins, 2011). Analyses of the public available data of cold-acclimated mice (GSE51080) indicated that chronic adaptation to 15°C for 2 weeks potently stimulates the mitochondrial BCAA catabolic pathway, including the expression of branched chain keto acid dehydrogenase E1 subunit alpha (BCKDHA), dihydrolipoamide branched chain transacylase (DBT), and the mitochondrial BCAA carrier Slc25a44 (MBC), as well as the expression of BAT thermogenic genes, such as Ucp1 and Ppargc1a (Figure 2A). Similarly, chronic administration of a β3-AR agonist (CL-316243, 0.1 mg/kg/day) for 7 days significantly activated the mitochondrial BCAA oxidation pathway in the BAT (Figure 2B).

Under these conditions of enhanced mitochondria BCAA oxidation, the PGE2-induced febrile response was significantly potentiated. This enhanced thermogenesis in BAT was accompanied by higher rectal temperature and inguinal WAT temperature following PGE2 injection (Figure 2C, D). In BAT, both cold acclimation and CL-316243 administration significantly increased total heat production (Δ°C × min), maximum temperature (Tmax), and the velocity of tissue temperature change (°C min−1) in response to an ICV administration of PGE2 (Figure 2E).

Mitochondrial BCAA carrier SLC25A44 is required for PGE2-induced fever

We next determined the extent to which mitochondrial BCAA entry via MBC/Slc25a44 is required for PGE2-induced febrile response. To this end, we first generated Slc25a44 floxed mice and then crossed them with Ucp1-Cre mice to generate BAT-specific MBC KO mice (Ucp1-Cre × Slc25a44flox/flox) and littermate control mice (Slc25a44flox/flox) (Figure 3A, B, Figure 3—figure supplement 1A). On a regular chow diet, BAT-specific MBC deletion did not alter body weight and tissue mass of metabolic organs, including the BAT, liver, WAT, and skeletal muscle (Figure 3C, Figure 3—figure supplement 1B, C). Morphologically, we found no major difference in brown adipocytes of BAT-specific MBC KO mice (Figure 3D, Figure 3—figure supplement 1D). The phenotype is consistent with our previous study in which neither CRISPRi-mediated knockdown of MBC nor BAT-specific deletion of BCKDHA altered brown adipocyte differentiation (Yoneshiro et al., 2019). However, UCP1+ cell-specific loss of MBC significantly reduced valine oxidation by 70% in the BAT (Figure 3E), reinforcing the requirement of MBC for mitochondrial BCAA oxidation in vivo. Remaining BCAA oxidation activity in the KO mice may arise from UCP1-negative cells within the BAT, such as endothelial cells, that avoid MBC deletion by Ucp1-Cre. No change in BCAA oxidation was seen in the skeletal muscle, a UCP1-negative tissue, of BAT-specific MBC KO mice.

Figure 3 with 1 supplement see all
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Mitochondrial branched chain-amino acid (BCAA) carrier SLC25A44/mitochondrial BCAA carrier (MBC) is required for prostaglandin E2 (PGE2)-induced fever.

(A) Generation of brown adipose tissue (BAT)-specific MBC knock-out (KO) mice (Ucp1-Cre; Slc25a44flox/flox; MBCUCP1 KO). (B) mRNA expression of Slc25a44 in the interscapular BAT (iBAT), skeletal muscle, and liver of BAT-specific MBC KO mice and the littermate control mice. n = 3 per group. (C) Tissue weight of the iBAT, ing-WAT, epi-WAT, liver, and gastrocnemius skeletal muscle of BAT-specific MBC KO mice (MBCUCP1 KO) and the littermate control mice. Control, n = 4; MBCUCP1 KO, n = 5. (D) Morphology and hematoxylin and eosin (H&E) staining of the iBAT of BAT-specific MBC KO mice and the littermate control mice. Scale bars, 50 μm. (E) Relative [1-14C] Val oxidation in the iBAT and gastrocnemius skeletal muscle of BAT-specific MBC KO mice (MBCUCP1 KO) and the littermate control mice. Control, n = 4; MBCUCP1 KO, n = 5. (F) Real-time temperature changes in the iBAT (ΔTBAT), rectum (ΔTRec), and ing-WAT (ΔTIng) of BAT-specific MBC KO mice (MBCUCP1 KO) and the littermate control mice. n = 7 per group. (G) Temperature changes during the first 20 min after intracerebroventricular (ICV) administration of PGE2 in (F). (H) Total heat production in the iBAT following ICV administration of PGE2 in (F). (I) Tmax of iBAT temperature following ICV administration of PGE2 in (F). (J) Velocity of iBAT temperature increase following ICV administration of PGE2 in (F). **p<0.01, ***p<0.001, n.s., not significant. Data were analyzed by using unpaired Student’s t-test (B, C, E, H–J) or two-way repeated measures ANOVA (F).

Figure 3—source data 1

Mitochondrial branched chain-amino acid (BCAA) carrier SLC25A44/mitochondrial BCAA carrier (MBC) is required for prostaglandin E2 (PGE2-)-induced fever.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig3-data1-v2.xlsx

When PGE2 was administered to the BAT-specific MBC KO mice at room temperature, we found that PGE2-induced febrile response was substantially attenuated relative to control mice (Figure 3F, G). Specifically, total heat production (Δ°C × min) and maximum temperature (Tmax) were significantly lower in BAT-specific MBC KO mice than those in control mice (Figure 3H, I). Of note, we observed no difference in the velocity of the initial rise in iBAT temperature (°C min−1) for the first 5 min after PGE2 administration between the two groups (Figure 3J). The data suggest that mitochondrial BCAA uptake via MBC is required for sustaining thermogenic activity in BAT, while it is dispensable for the initiation of thermogenesis following PGE2 administration.

Mitochondrial BCAA catabolism controls PGE2-induced thermogenesis via UCP1-dependent and UCP1-independent mechanisms

To test if the above phenotype of BAT-specific MBC KO mice is due to reduced BCAA oxidation, we next examined the extent to which genetic loss of BCKDHA, a mitochondria-localized BCAA oxidation enzyme, affects the PGE2-induced febrile response. We previously reported that BAT-specific BCKDHA KO mice (Ucp1-Cre × Bckdhaflox/flox) exhibited impaired BCAA oxidation, systemic BCAA clearance, and thermogenesis in BAT (Yoneshiro et al., 2019). Consistent with the phenotype seen in BAT-specific MBC KO mice, we found that PGE2-induced BAT thermogenesis was attenuated in the BAT-specific BCKDHA KO mice relative to control mice (Figure 4A). It is notable that total heat production (Δ°C × min) and maximum temperature (Tmax) in the BAT were significantly lower in the BCKDHA KO mice than those in control mice (Figure 4B, C), whereas no difference was seen in the velocity of the initial BAT temperature change (°C min−1) between the genotypes (Figure 4D). These results further support the view that mitochondrial BCAA catabolism through the actions of MBC and BCKDH is required for the maintenance of PGE2-induced BAT thermogenesis, but not required for the initiation of thermogenesis.

Figure 4
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Mitochondrial branched chain-amino acid (BCAA) oxidation triggers thermogenesis via UCP1-dependent and UCP1-independent mechanisms.

(A) Real-time temperature changes in the interscapular BAT (iBAT) of BCKDHAUCP1knock-out (KO) and the littermate control mice following intracerebroventricular (ICV) administration of prostaglandin E2 (PGE2). n = 5 per group. (B) Total heat production in the iBAT of indicated mice following ICV administration of PGE2 in (A). (C) Tmax of iBAT temperature following ICV administration of PGE2 in (A). (D) Velocity of iBAT temperature increase following ICV administration of PGE2 in (A). (E) Real-time temperature changes in the iBAT and rectum of UCP1 KO mice following ICV injection of PGE2. n = 5 per group. (F) Oxygen consumption rate (OCR) in brown adipocytes derived from wild-type mice (control) or UCP1 KO mice. Differentiated adipocytes in the BCAA-free medium were treated with valine (Val) or vehicle (Veh), and subsequently stimulated with norepinephrine (NE) at indicated time points. OCR values were normalized by total protein (µg). n = 10 per group. (G) OCR in beige adipocytes derived from wild-type mice (control) or UCP1 KO mice. Differentiated adipocytes in the BCAA-free medium were treated with valine (Val) or vehicle (Veh), and subsequently stimulated with NE at indicated time points. OCR values were normalized by total protein (µg). Control + vehicle, n = 9; Control + Val n=8; UCP1 KO + vehicle, n = 6; UCP1 KO + Val, n = 9. (H) mRNA expression of Serca2b in UCP1 KO beige adipocytes expressing a scrambled control (Scr, n = 4) or two independent shRNAs targeting Atp2a2 (#1 and #2, n = 6 per group). (I) Relative [1-14C] Val oxidation in UCP1 KO beige adipocytes in (H). Differentiated adipocytes were cultured in the presence of NE or vehicle. Valine oxidation was measured using [1-14C] valine and normalized by total protein (μg). Vehicle n = 6, NE n = 5, except sh-Atp2a2 #1 treated with NE n = 6. (J) OCR was measured in UCP1 KO beige adipocytes in (H). Differentiated adipocytes were incubated in the BCAA-free media supplemented with Val (sh-Scr, n = 9; sh-Atp2a2, n = 6) or vehicle (sh-Scr, n = 6; sh-Atp2a2, n = 7), and subsequently stimulated with NE. OCR values were normalized by total protein (μg). *p<0.05, **p<0.01, ***p<0.001, n.s., not significant. Data were analyzed by unpaired Student’s t-test (B–D), one- (H) or two-way (I) factorial ANOVA followed by Tukey’s post hoc test, or two-way repeated measures ANOVA (A, F, G) followed by Tukey’s post hoc test (J).

Figure 4—source data 1

Mitochondrial branched chain-amino acid (BCAA) oxidation triggers thermogenesis via UCP1-dependent and UCP1-independent mechanisms.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig4-data1-v2.xlsx

Cold-induced thermogenesis in iBAT requires UCP1 (Enerbäck et al., 1997). This UCP1 dependency in iBAT is attributed to the fact that brown adipocytes have a low ATP synthesis capacity (Kramarova et al., 2008), and thus, ATP-dependent (i.e., UCP1-independent) futile cycle, such as Ca2+ cycling or creatine cycling (Ikeda et al., 2017; Kazak et al., 2015) may not compensate for the lack of UCP1. Nonetheless, several studies reported that UCP1 is dispensable for febrile responses to i.p. administration of LPS or interleukin (IL)-1β (Okamatsu-Ogura et al., 2007; Riley et al., 2016; Eskilsson et al., 2020). Accordingly, we examined if ICV administration of PGE2 induces UCP1-dependent thermogenesis in iBAT. In mice kept under a room temperature condition, we found that PGE2-induced thermogenesis was totally blunted in UCP1 KO mice (Figure 4E). The data are consistent with the result in cultured brown adipocytes in which BCAA supplementation enhanced norepinephrine (NE)-stimulated cellular respiration in an UCP1-dependent manner (Figure 4F). In contrast, BCAA supplementation in UCP1 KO beige adipocytes significantly enhanced NE-stimulated cellular respiration, although the effect was less than that in wild-type (WT) beige adipocytes (WT: +46.4 ± 1.2%, UCP1 KO: +30.6 ± 2.5%, p<0.001, Figure 4G).

Given our previous works on the mechanism of Ca2+ cycling thermogenesis via SERCA2 (Ikeda et al., 2017), we next determined the extent to which SERCA2-mediated Ca2+ cycling mediates BCAA catabolism and thermogenesis. To this end, we depleted SERCA2 (encoded by Atp2a2) using two independent shRNAs targeting Atp2a2 in UCP1 null beige adipocytes (Figure 4H). In beige adipocytes, NE treatment significantly stimulated Val oxidation even in the absence of UCP1; however, the NE-induced BCAA oxidation was near completely blunted when SERCA2 was depleted (Figure 4I). Importantly, depletion of SERCA2 eliminated the stimulatory effect of BCAA supplementation on UCP1-independent respiration following NE treatment (Figure 4J). These results suggest that mitochondrial BCAA oxidation enhances thermogenesis in brown fat and beige fat through UCP1-dependent and independent mechanisms, respectively.

Metabolic flexibility to mitochondrial BCAA catabolism is required for sustained thermogenesis

Fatty acids and glucose are considered to be the primary fuel for BAT thermogenesis, while the contribution of BCAA as a carbon fuel appears marginal even though BAT is a major metabolic-sink for BCAA (Yoneshiro et al., 2019; López-Soriano et al., 1988; Neinast et al., 2019b; Hui et al., 2020). Nonetheless, our data raise the possibility that mitochondrial BCAA catabolism (i.e., mitochondrial import, deamination, and oxidation) is needed for sustaining thermogenic activity even under conditions in which the primary fuels are not limited. To probe this, we cultured differentiated brown adipocytes in the presence of glucose at a physiological level (5 mM) and measured OCR in response to NE. NE treatment rapidly increased OCR within 5–6 min, whereas this effect gradually declined. However, the supplementation of Leu after NE effectively maintained the elevated levels of OCR (Figure 5A). On the other hand, such a stimulatory effect of Leu was completely lost in MBC KO brown adipocytes, although these cells were able to respond to NE and increased OCR (Figure 5B). The stimulatory effect is not restricted to Leu because supplementation of Val or Ile also significantly augmented norepinephrine-induced thermogenesis to the same extent to Leu in an MBC-dependent manner (Figure 5C).

Figure 5
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Mitochondrial branched chain-amino acid (BCAA) catabolism required for sustained thermogenesis.

(A) Oxygen consumption rate (OCR) normalized to total protein (in μg) in control brown adipocytes. Differentiated adipocytes in BCAA-free medium with 5 mM glucose were stimulated with norepinephrine (NE), and subsequently supplemented with Leu or vehicle. n = 9 per group. (B) OCR normalized to total protein (in μg) in mitochondrial BCAA carrier (MBC) knock-out (KO) brown adipocytes. Differentiated adipocytes cultured in BCAA-free medium with glucose (5 mM) were stimulated with NE, and subsequently supplemented with Leu or vehicle. n = 9 per group. (C) NE-stimulated OCR in control and MBC KO brown adipocytes. Differentiated adipocytes in BCAA-free medium, containing 5 mM glucose, supplemented with Val, Leu, or Ile were stimulated with NE for 30 min. n = 6 per group. (D) OCR normalized to total protein (in μg) in control brown adipocytes. Differentiated adipocytes in BCAA-free medium with glucose (20 mM) were supplemented with Leu or vehicle, and subsequently stimulated with NE. n = 5 per group. (E) OCR normalized to total protein (in μg) in MBC KO brown adipocytes. Differentiated adipocytes in BCAA-free medium with glucose (20 mM) were supplemented with Leu or vehicle, and subsequently stimulated with NE. n = 5 per group. (F) Lactate production in control and MBC KO brown adipocytes. Differentiated adipocytes were stimulated with vehicle or NE for 30 min, and lactate content in the medium was measured. n = 3 per group. *p<0.05, **p<0.01, ***p<0.001, n.s., not significant. Data were analyzed by two-way repeated measures ANOVA (A, B, D, E) or two-way factorial ANOVA followed by Tukey’s post hoc test (C, F).

Figure 5—source data 1

Mitochondrial branched chain-amino acid (BCAA) catabolism required for sustained thermogenesis.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig5-data1-v2.xlsx

The effect of BCAA supplementation on OCR is to potentiate the action of thermogenic stimuli: when Leu was supplemented in brown adipocytes prior to NE treatment, we observed no increase in OCR. However, NE-induced thermogenesis was significantly enhanced when Leu was supplemented even in the presence of high glucose at 20 mM (Figure 5D). Importantly, this effect of Leu was not seen in the absence of MBC (Figure 5E). Consistent with the previous reports that activation of the β-AR pathway stimulates both glucose oxidation and lactate production in brown adipocytes (Olsen et al., 2014; Ikeda et al., 2017), NE treatment in differentiated brown adipocytes increased lactate production. Notably, MBC loss led to higher production of lactate than control cells (Figure 5F), suggesting that MBC KO cells were limited to utilize glucose even in the presence of Leu.

MBC is required for the synthesis of the mitochondrial amino acid pool and TCA intermediates

To address how MBC controls BCAA catabolism, we next performed uniformly 13C-labeled, 15N-labeled Leu ([U-13C6, 15N1] Leu) tracing in differentiated brown adipocytes (Figure 6—figure supplement 1A). As we previously reported (Yoneshiro et al., 2019), brown adipocytes dominantly express BCAA aminotransferase 2 (BCAT2), the mitochondria-localized form of BCAT, and thus, deamination and oxidation of BCAA largely occur in the mitochondrial matrix (Figure 6A). GC-MS analysis of intracellular metabolites revealed that levels of Leu, α-ketoisocaproate (KIC), Ala, and Glu, were significantly lower in MBC KO brown adipocytes than those in WT control cells (Figure 6B). There was a trend towards lower Asp levels in MBC KO cells relative to WT control cells, although the difference was not statistically significant. This is likely because BAT expresses very low levels of aspartate aminotransferase (GOT), the enzyme that catalyzes the conversion of oxaloacetate to Asp, whereas BAT expresses high levels of glutamate-pyruvate transaminase (GPT) that catalyzes the reversible conversion of Ala and α-ketoglutarate (α-KG) to Glu and pyruvate (Figure 6—figure supplement 1B). Importantly, the reduced levels of KIC, Glu, and Ala in MBC KO cells were due to the reduced conversion from Leu because levels of labeled KIC, Glu, and Ala (i.e., Leu-derived) were significantly lower in KO cells than those in WT control cells (Figure 6C, D). Also, there was a slight but significant reduction in M3-labeled Asp in KO cells relative to control cells.

Figure 6 with 1 supplement see all
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Mitochondrial BCAA carrier (MBC) is required for the synthesis of the mitochondrial amino acids and TCA intermediates.

(A) Schematic illustration of mitochondrial branched chain-amino acid (BCAA) fate to the TCA cycle and amino acid synthesis. (B) Amino acid relative abundance in wild-type (WT) control and MBC knock-out (KO) brown adipocytes as determined by 13C-Leu metabolomics. Cells were harvested at a basal state. n = 4 per group. (C) Leu-derived 13C labeling in KIC in WT control and MBC KO brown adipocytes in (B). (D) Labeling in indicated amino acids derived from Leu in WT control and MBC KO brown adipocytes in (B). (E) Norepinephrine (NE)-induced changes in TCA cycle intermediates in WT control and MBC KO brown adipocytes. Cells were harvested at the indicated time points following NE treatment in (B). (F) The relative abundance of indicated TCA cycle intermediate in WT control and MBC KO brown adipocytes at 1 hr following NE treatment in (B). (G) Leu-derived 13C labeling in TCA cycle intermediates in WT control and MBC KO brown adipocytes. Cells were harvested at 1 hr following NE treatment in (B). (H) Mole percentage enrichment (MPE) of TCA cycle intermediates derived from [U-13C6] Leu in control and MBC KO brown adipocytes. Cells were harvested at 1 hr following NE treatment. n = 4 per group. Data in 6B-H was normalized to a norvaline internal standard. *p<0.05, **p<0.01, ***p<0.001. Data were analyzed by unpaired Student’s t-test (B–D, F–H) or two-way factorial ANOVA followed by post hoc unpaired t-test (E).

Figure 6—source data 1

Mitochondrial BCAA carrier (MBC) is required for the synthesis of the mitochondrial amino acids and TCA intermediates.

https://cdn.elifesciences.org/articles/66865/elife-66865-fig6-data1-v2.xlsx

Following the deamination of Leu in the mitochondria, KIC fuels the TCA cycle in brown adipocytes. Our previous study showed that NE treatment significantly increased the Leu-derived TCA cycle intermediates (Yoneshiro et al., 2019). Consistent with this prior observation, we found that intracellular levels of α-KG, succinate, malate, and citrate increased after NE treatment; however, the increases in α-KG and malate levels occurred at significantly less degree in MBC KO cells (Figure 6E). Importantly, the total pool size of TCA cycle intermediates in MBC KO cells was smaller than that in WT control cells at 60 min after NE treatment (Figure 6F), although the differences were not seen at basal state (before NE treatment) (Figure 6—figure supplement 1C). These results are likely relevant to the finding that mitochondrial BCAA catabolism is required for sustaining BAT thermogenesis, but not for the initial trigger of thermogenesis. Even under the reduced pool size, the contribution of Leu into the TCA cycle, as shown by 13C ion counts and the mole percentage enrichment (MPE), was lower in MBC KO cells than that in WT control cells (Figure 6G, H). Of note, the MPE of TCA intermediates was lower than our previous study that achieved ~20% (Yoneshiro et al., 2019). This difference arose from the fact that the present study incubated cells with 13C-labeled Leu for 30 min and subsequently washed off before NE treatment, whereas the previous study used a protocol in which cells were labeled for 1 hr during NE treatment.

Together, the present data suggest the following model (Figure 7). In response to febrile stimuli, such as increased PGE2 or psychological stress, mitochondrial BCAA catabolism is activated along with enhanced BAT thermogenesis. The sympathetically stimulated mitochondrial BCAA catabolism is required for maintaining active BAT thermogenesis to sustain febrile responses. Mechanistically, MBC is a critical gatekeeper of mitochondrial BCAA transport and subsequent catabolic reactions, including deamination as well as the synthesis of mitochondrial amino acid pool and TCA intermediates.

Figure 7
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A model of mitochondrial branched chain-amino acid (BCAA) catabolism and brown adipose tissue (BAT) thermogenesis in response to fever stimuli.

In response to intracerebroventricular (ICV) administration of prostaglandin E2 (PGE2) or psychological stress, mitochondrial BCAA catabolism in the BAT is activated along with enhanced thermogenesis. The fever-induced mitochondrial BCAA catabolism is required for sustaining thermogenesis. Mitochondrial BCAA uptake via mitochondrial BCAA carrier (MBC) is required for BCAA deamination and the synthesis of mitochondrial amino acid pool and TCA intermediates.

Discussion

In general, hyperthermic responses to pyrogens are considered beneficial because the elevation of body temperature can prevent the replication of infective pathogens, while activating innate immunity (e.g., enhanced cytokine release). However, persistent thermogenesis, often associated with psychological stress-induced hyperthermia, malignant hyperthermia, traumatic brain injury, and endocrine fever, causes severe exhaustion and, in the worst cases, leads to widespread cellular and organ damage, such as renal injury, liver failure, and edema (Walter et al., 2016).

Fever involves multiple involuntary effector responses besides BAT thermogenesis, including skeletal muscle shivering and cutaneous vasoconstriction (Morrison and Nakamura, 2019). Hence, experimental setting, such as the types of pyrogen and anesthetizer, would influence the data interpretation. For instance, UCP1 null mice exhibit fever in response to systemic administration (i.p. injection) of LPS or IL-1β under a non-anesthetized condition (Okamatsu-Ogura et al., 2007; Riley et al., 2016; Eskilsson et al., 2020). The difference from the present study is due to the fact that, at room temperature, BAT thermogenesis can be compensated by involuntary (e.g., shivering, vasoconstriction) and behavioral (e.g., increased locomotion) responses until body temperature reaches to a set-point in the pyrogen-sensitized thermoregulatory circuitry of the brain (Nakamura, 2011; Morrison and Nakamura, 2019). On the other hand, the present temperature recording in anesthetized mice excludes such responses and specifically determines the contribution of non-shivering thermogenesis to febrile responses in response to the ICV administration of PGE2. In this regard, the contribution of skeletal muscle to circulating BCAA (e.g., protein breakdown) would be minimum in our study. It is likely that the primary source of circulating BCAAs is food-derived, although microbiome could be an alternative source (Pedersen et al., 2016).

Nonetheless, the present study demonstrates that mitochondrial BCAA catabolism plays a vital role in maintaining BAT thermogenesis to sustain febrile responses, and thus suggests a new opportunity to soothe persistent fever by blocking this pathway. Conversely, it is conceivable that enhancing BCAA catabolism is effective for elderly populations in which approximately 20–30% of the elderly show blunted or absent febrile response to pyrogens (Norman, 2000). It is worth noting that the thermogenic capacity of BAT is significantly attenuated in aging, and that this attenuation is closely coupled with reduced BCAA oxidation (Tajima et al., 2019). This age-associated attenuation in BCAA oxidation is attributed, in part, to reduced protein lipoylation in the E2 subunit of the BCKDH complex, while dietary supplementation of α-lipoic acids effectively restores the protein lipoylation of BCKDH and thermogenic function of BAT in old mice (Tajima et al., 2019). Since a blunted febrile response to infections represents a poorer prognosis in the elderly (Norman, 2000), enhancing BCAA catabolism, for example, by α-lipoic acid supplementation or inhibition of BCKDH kinase activity (BDK, an inhibitory kinase of BCKDH), may represent effective means to alleviate age-associated decline in fever responses.

BCAAs are more than fuel in thermogenic fat

It has been well appreciated that lipolysis-derived fatty acids are the primary fuel for thermogenesis in brown and beige fat (Chouchani and Kajimura, 2019). Indeed, blockade of lipolysis in adipose tissues, by genetically deleting adipose triglyceride lipase (ATGL) or the ATGL-activating protein comparative gene identification-58 (CGI-58) in adipocytes, potently attenuates BAT thermogenesis in mice (Schreiber et al., 2017; Shin et al., 2017). On the other hand, the contribution of BCAA to the TCA cycle appears minor relative to fatty acids or glucose in BAT (Hui et al., 2020), although BAT is a significant metabolic sink for BCAA when activated (Yoneshiro et al., 2019; López-Soriano et al., 1988; Neinast et al., 2019b). This is aligned with the present results that mitochondrial BCAA uptake and oxidation are required for the maintenance, rather than the initiation, of BAT thermogenesis (see Figures 3 and 4). Presumably, BAT is able to initiate the rising phase of febrile thermogenesis by utilizing fatty acids and glucose even in the absence of BCAA.

We speculate the following possibilities as to why mitochondrial BCAA catabolism is required in BAT: The first possibility is the role of BCAA catabolic products as replenishment of TCA cycle intermediates. Complete oxidation of acetyl-CoA from β-oxidation requires the condensation of acetyl-CoA and oxaloacetate in the TCA cycle. Generation of the anaplerotic products from BCAA oxidation (see Figure 6) may allow for sustaining fatty acid oxidation in the mitochondrial matrix. The second possibility is the role of BCAA-derived nitrogen in the mitochondria. Given the role of BCAAs as major nitrogen donors, deamination of BCAAs by BCAT2 is critical for the synthesis of mitochondrial amino acid pool, including Glu, Ala, and Asp. Indeed, all three BCAAs (Val, Leu, Ile) similarly augmented NE-stimulated respiration in an MBC-dependent manner. Also, thermogenic stimuli activate the purine and pyrimidine synthesis pathway in BAT (Lu et al., 2017), and hence, BCAA-derived nitrogen could contribute to nucleotide synthesis. Pertinent to the finding, our recent study reports that MBC overexpression upregulates the expression of SLC7A5 (LAT1), the plasma membrane transporter for neutral amino acids, including BCAAs (Walejko et al., 2021). Third, BCAA catabolism may promote de novo lipogenesis by generating monomethyl branched-chain fatty acids (mmBCFAs) as previously reported (Green et al., 2016; Wallace et al., 2018). BAT is a major site of mmBCFA synthesis in which the expression of mmBCFA synthesis enzymes, such as carnitine acetyltransferase (CrAT), is increased after 1-month-cold acclimatization (Wallace et al., 2018). This pathway is activated during chronic cold adaptation (3 weeks and after) (Yoneshiro et al., 2019), and thus, BCAA may contribute to mmBCFA synthesis under a cold-acclimated state. Together, the role of BCAA in thermogenic fat is likely more than merely a carbon source of fuel into the TCA cycle.

The role of mitochondrial carriers in metabolic flexibility

Metabolic flexibility is a term that often describes the ability of cells, organs, or an organism to shift the principal types of fuel in order to meet their metabolic demands in response to changes in external and internal conditions. A well-appreciated example is in the skeletal muscle upon exercise in which acute and high-intensity exercise utilizes glucose oxidation, while aerobic and endurance exercise triggers a fuel switch toward fatty acid oxidation (Smith et al., 2018; Goodpaster and Sparks, 2017). Importing necessary metabolites into the mitochondrial matrix (e.g., acyl-CoA for fatty acids) is an essential step of metabolic flexibility: for instance, blockade of carnitine shuttle by deleting carnitine palmitoyltransferase 1 (CPT1) attenuates muscle function and endurance exercise capacity in mice (Wicks et al., 2015). It is pertinent to note that genetic mutations in carnitine-acylcarnitine translocase (encoded by SLC25A20), which mediates the transport of acylcarnitines into the mitochondrial matrix, cause severe metabolic disorders, including hypoglycemia, myopathy, and muscle weakness in humans (Fukushima et al., 2013; Iacobazzi et al., 2004).

The present study found that when stimulated with NE, brown adipocytes lacking MBC increase lactate production, suggesting a shift to glucose utilization even in the presence of BCAA. This metabolic inflexibility is accompanied by an impairment in sustained thermogenic activity in brown adipocytes. Of particular note, impaired BCAA oxidation in peripheral metabolic organs and concomitant elevation of circulating BCAA levels are a metabolic signature of obesity, insulin resistance, and type 2 diabetes (Felig et al., 1969; Wang et al., 2011; Newgard et al., 2009; Würtz et al., 2013). Quantitative BCAA tracing shows that reduced BCAA oxidation in the liver and adipose tissues re-distributes BCAA into the muscle, leading to BCAA overload and insulin resistance (Neinast et al., 2019b). Thus, future studies are needed to determine the role of MBC in the pathogenesis of insulin resistance.

Materials and methods

Animals

All the animal experiments were performed following the guidelines by the UCSF Institutional Animal Care and Use Committee (AN165833) or by the Nagoya University Animal Experiment Committee, and approved by the committees. The WT and UCP1 KO mice aged ~14 weeks had free access to food and water, 12 hr light cycles, and were caged at 23°C. BAT-specific Bckdha KO mice were obtained by crossing Bckdha floxed mice with Ucp1-Cre mice, as reported previously (Yoneshiro et al., 2019). For the generation of BAT-specific Slc25a44/MBC KO mice (MBCUCP1 KO mice), Slc25a44 floxed mice were obtained from the Applied StemCell (MC185, Milpitas, CA, USA) and crossed with Ucp1-Cre mice. All mice were C57BL/6 background. Adult male Sprague–Dawley (SD) rats were housed two or three to a cage with ad libitum access to food and water at 24°C with a standard 12 hr light/dark cycle.

Cold acclimatization and treatment with β3 adrenergic receptor agonist

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WT mice were acclimated to either thermoneutral temperature at 30°C (n = 5) or cold temperature at 15°C (n = 5) for 2 weeks and were used for temperature recording in fever response. UCP1 KO mice and the littermate WT mice (control) were treated with saline (control n = 4, UCP1 KO n = 5) or 0.1 mg/kg/day of CL-316243, β3 adrenergic receptor agonist (control n = 5, UCP1 KO n = 6) for 1 week and were used for temperature recording in fever response.

Temperature recordings in febrile response

Mice under anesthesia with urethane (1.3 mg/kg) were positioned in a stereotaxic apparatus according to the mouse brain atlas (Franklin and Paxinos, 2008). A stainless steel cannula (outer diameter, 0.35 mm) and a 1 ml disposable syringe were connected with polyethylene tubing and were inserted perpendicularly into the right lateral ventricle (coordinates: 0.1 mm posterior to bregma, 0.1 mm lateral to the midline, and 1 mm ventral to the brain surface). Then, mice were left on a self-regulating heating pad to stabilize the rectal temperature (TRec) at 37°C and implanted with a type T thermocouple probe (IT-18, Physitemp, Clifton, NJ) in the rectum and with needle microprobes (MT-29/1, Physitemp) in the interscapular BAT and inguinal WAT (Yoneshiro et al., 2019). Tissue temperatures were simultaneously recorded by TC-2000 Meter (Sable Systems International). When tissue temperatures were stable, for >5 min, PGE2 (1.4 μg; Sigma) in 1.4 μl of pyrogen-free saline or only saline was injected into the ventricle through the cannula. The changes in tissue temperatures were contentiously measured every second for 1 hr or as indicated, and the mean value per minute was calculated.

Tissue histology

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For hematoxylin and eosin (H&E) staining, tissues of mice were fixed in 4% paraformaldehyde overnight at 4°C, followed by dehydration in 70% ethanol. After the dehydration procedure, tissues were embedded in paraffin, sectioned at a thickness of 5 μm, and stained with H&E following the standard protocol. Images of tissue samples were captured using the Inverted Microscope Leica DMi8.

Ex vivo BCAA oxidation

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Isolated tissue (20–30 mg) was placed in a polypropylene round-bottom tube and incubated in the 1 ml KRB/HEPES buffer containing 0.16 μCi/ml [1-14C] Val at 37°C for 1 hr. After adding 350 μl of 30% hydrogen peroxide in the tube, [14C] CO2 was trapped in the center well supplemented with 300 μl of 1 M benzethonium hydroxide solution for 20 min at room temperature. BCAA oxidation was quantified by counting radioactivity of trapped [14C] CO2 using a scintillation counter.

Cell culture

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Immortalized brown and beige adipocytes from C57BL/6 mice and UCP1 KO brown and beige adipocytes were generated in our previous studies (Yoneshiro et al., 2019; Ikeda et al., 2017). Adipocyte differentiation was induced by treating confluent preadipocytes with DMEM containing 10% FBS, 0.5 mM isobutylmethylxanthine, 125 nM indomethacin, 2 μg/ml dexamethasone, 850 nM insulin, 1 nM T3, and 0.5 μM rosiglitazone. Two days after induction, cells were switched to a maintenance medium containing 10% FBS, 850 nM insulin, 1 nM T3, and 0.5 μM rosiglitazone (Ohno et al., 2012). The cells were fully differentiated 6–7 days after inducing differentiation.

Generation of Slc25a44/MBC KO brown adipocytes

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For the generation of Slc25a44/MBC KO brown adipocytes, preadipocytes isolated from BAT of Slc25a44flox/flox mice were immortalized by using the SV40 Large T antigen as described previously (Yoneshiro et al., 2019) and subsequently infected with a retrovirus containing either empty vector or Cre (#34565, Addgene), followed by hygromycin selection at a dose of 200 μg/ml.

Cellular respiration

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Oxygen consumption rate (OCR) in cultured adipocytes was measured using the Seahorse XFe Extracellular Flux Analyzer (Agilent) in a 24-well plate. For measurement of NE-induced respiration in the presence and absence of BCAA, differentiated adipocytes were maintained either in KRB/HEPES buffer containing 20 or 5 mM glucose, 200 nM adenosine, 2% BSA (bovine serum albumin), or in BCAA-free DMEM (Dulbecco's modified Eagle medium), which was a kind gift from Nissui Pharmaceutical Co. Ltd. During OCR measurement, cells were treated with 2 mM Val, Leu, Ile, or vehicle, and subsequently treated with NE (1 μM) at the indicated time point.

Stable isotope-labeled leucine metabolome analysis

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To determine the effect of MBC depletion on the metabolic fate of BCAA in brown adipocytes, we used [13C6, 15N1] Leu tracing. Differentiated MBC KO or control brown adipocytes were incubated in the BCAA-free medium supplemented with [13C6, 15N1] Leu (608068, Sigma-Aldrich) and were harvested at 0, 0.5, and 1 hr after the treatment with NE. Metabolites were then extracted using by scraping cells in 3 ml chilled 100% MeOH (LC-MC grade). The extracts were then centrifuged at 4°C and 14,400 × g for 10 min, and the clarified aqueous phase was transferred to a fresh Eppendorf and stored in −80°C until processing for GC-MS analysis. For GC-MS analysis, 10 μl of 0.05 mM norvaline was added to 100 μl of extracted metabolites and dried under N2 gas-flow at 37°C using an evaporator. Amino and organic acids were derivatized via methoximation and silylation. In brief, metabolites were resuspended in 25 μl of methoxylamine hydrochloride (2% [w/v] in pyridine) and incubated at 40°C for 90 min on a heating block. After brief centrifugation, 35 μl of MTBSTFA + 1% TBDMS was added and the samples were incubated at 60°C for 30 min. GC-MS analysis was performed on an Agilent 7890B GC system equipped with a HP-5MS capillary column connected to an Agilent 5977A Mass Spectrometer 50. Mass isotopomer distributions were obtained by integration of ion chromatograms 51 and corrected for natural isotope abundances Relative levels of metabolites or isotopomers were calculated by normalizing to norvaline. MPE of isotopes, an index of isotopic enrichment of metabolites, was calculated as the percent of all atoms within the metabolite pool that are labeled according to the established formula (Wallace et al., 2018).

RNA preparation and quantitative RT-PCR

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Total RNA was extracted from tissue or cells using RNeasy mini-kit (Qiagen), and cDNA was synthesized using iScript cDNA Synthesis kit (BioRad) according to the manufactural protocols. qRT-PCR was performed using an ABI ViiA7 PCR cycler. The primer sequences are listed in Supplementary file 1. The gene expression levels were normalized to internal control 36B4 levels (Yoneshiro et al., 2019).

Immunoblotting

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Protein lysates from isolated BAT were extracted using Qiagen TissueLyzer LT and RIPA lysis and extraction buffer (Thermo Fisher) and cOmplete protease inhibitors (Roche). Tissue lysates were applied to immunoblot analysis using the UCP1 antibody (Amcam, ab10983, 1:2000). β-Actin (Sigma, A3854, 1:40,000) was used as a loading control for each sample.

Statistical analyses

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All data were expressed as the means with SEMs and analyzed by using statistical software (SPSS 25.0; IBM Japan, Tokyo, Japan). Comparisons between the two groups were analyzed using the paired t-test or the Student's t-test, as appropriate. Analysis of variance (ANOVA) followed by Tukey’s test was used for multiple-group comparisons. Two-way repeated-measures ANOVA was used for the comparisons of repeated measurements. Two-tailed p value ≤ 0.05 was considered as statistically significant.

Data availability

All data generated or analyzed during this study are included in the manuscript as source data files.

The following previously published data sets were used
    1. Christian M
    2. Rosell M
    3. Frontini A
    4. Cinti S
    5. Kaforou M
    6. Montana G
    (2014) NCBI Gene Expression Omnibus
    ID GSE51080. Expression data from exposure of BAT and WAT at 6 and 28 degrees C.
    https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE51080
    1. Tajima K
    2. Ikeda K
    3. Chang HY
    4. Chang CH
    5. Yoneshiro T
    6. Oguri Y
    7. Jun H
    8. Wu J
    9. Ishihama Y
    10. Kajimura S
    (2019) ArrayExpress
    ID E-MTAB-7445. RNA-seq of age-associated transcriptome changes in brown adipose tissue.
    https://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-7445/
    1. Wu C
    2. Orozco C
    3. Boyer J
    4. Leglise M
    5. Goodale J
    6. Batalov S
    7. Hodge CL
    8. Haase J
    9. Janes J
    10. Huss JW
    11. Su AI
    (2009) BioGPS, GeneAtlas MOE430
    ID gcrma. BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources.
    http://biogps.org/#goto=welcome

References

  8. Book
    1. Franklin K
    2. Paxinos G
    (2008)
    The Mouse Brain in Stereotaxic Coordinates
    Academic Press.
    1. Nakamura K
    (2011) Central circuitries for body temperature regulation and fever
    American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 301:R1207–R1228.
    https://doi.org/10.1152/ajpregu.00109.2011
    1. Norman DC
    (2000) Fever in the elderly
    Clinical Infectious Diseases 31:148–151.
    https://doi.org/10.1086/313896

Decision letter

  1. Ralph J DeBerardinis
    Reviewing Editor; UT Southwestern Medical Center, United States
  2. David E James
    Senior Editor; The University of Sydney, Australia
  3. Ralph J DeBerardinis
    Reviewer; UT Southwestern Medical Center, United States

In the interests of transparency, eLife publishes the most substantive revision requests and the accompanying author responses.

Acceptance summary:

Febrile responses require thermogenesis by the brown adipose tissue, but the fuels used to generate heat in this context are incompletely understood. Here the authors identify transport of branched chain amino acids into the mitochondria as an essential component of febrile responses to pyrogens and physiological stress in rodents. Genetic deletion of the mitochondrial branched chain amino acid transporter SLC25A44 from brown adipose tissue blunts these responses and alters nutrient utilization in brown adipocytes.

Decision letter after peer review:

Thank you for submitting your article "Metabolic flexibility via mitochondrial BCAA carrier SLC25A44 is required for optimal fever" for consideration by eLife. Your article has been reviewed by 3 peer reviewers, including Ralph J DeBerardinis as the Reviewing Editor and Reviewer #1, and the evaluation has been overseen by David James as the Senior Editor.

The reviewers have discussed their reviews with one another, and the Reviewing Editor has drafted this to help you prepare a revised submission.

Essential revisions:

1. Where is the level of BCAA regulation after PGE2 or CL treatment? Does this occur via enhanced uptake across the plasma membrane or enhanced uptake into the mitochondria? Does BCAA uptake in isolated mitochondria increase after treatment with PGE2 or β-3-AR agonists?

2. In interpreting the data on the PGE2-mediated thermogenic response, it would be helpful to know whether UCP1 protein expression is increased in the brown adipose tissue.

3. Regarding the data in Figure 4F and 5A-D, the authors write "However, norepinephrine-induced thermogenesis was significantly enhanced when Leu was supplemented even in the presence of high glucose at 20 mM (Figure 5C). Importantly, this effect of Leu was not seen in the absence of MBC (Figure 5D)." This is confusing: In Figure 5C and D, Val is shown. Can the authors directly compare the O2 consumption response of MBC-KO adipocytes to the three amino acids individually – valine, leucine and isoleucine (with and without high glucose) – administered during NE activation?

4. The relevance of the enhanced glycolysis observed in Figure 5E is unclear. Converting glucose to lactate should not support thermogenesis if UCP1 and therefore oxidative mitochondrial metabolism is required. Does NE stimulation induce glucose oxidation in addition to increased lactate formation under these conditions, and is this effect further enhanced in MBC-deficient BAT?

Reviewer #1:

This manuscript describes the role of BCAA metabolism in PGE2-mediated fever. The authors find that BAT-specific knockout of the mitochondrial BCAA carrier SLC25A44 (MBC) results in blunted thermogenesis following intracerebroventricular PGE2 administration. The febrile state is associated with increased expression BCAA-related genes including MBC in BAT and marked depletion of BCAAs from the circulation. BAT-specific knockout of BCKDHA, which catalyzes the rate-limiting step of mitochondrial BCAA oxidation, also blunts PGE2-mediated fever. Isolated BAT tissue from mice exposed to PGE2 or psychological stress reveals enhanced BCAA oxidation, and providing excess BCAAs in these culture-based experiments allows BAT to sustain respiration stimulated by norepinephrine. Metabolomics and stable isotope tracing studies indicate that MBC knockout results in suppressed pools of TCA cycle intermediates and some nonessential amino acids. The authors conclude that MBC-mediated BCAA oxidation is required to fuel ongoing thermogenesis during febrile responses. Overall, the experiments are performed to a high standard, make use of genetic mouse models, and support a clear narrative of the role of MBC in thermogenesis stimulated by central PGE2 administration.

1. As the authors point out in the Discussion, the metabolic effects of BCAA degradation can include anaplerosis and/or the production of acetyl-CoA. This makes the respiration experiments in Figure 5 difficult to interpret, because Leu (used in Figure 5A,B) generates acetyl-CoA, whereas Val (Figure 5C,D) is anaplerotic. The effects on respiration may therefore differ. Can the authors harmonize these experiments by using the same amino acid for all conditions?

2. The relevance of the enhanced glycolysis observed in Figure 5E is unclear. Converting glucose to lactate should not support thermogenesis if UCP1 and therefore oxidative mitochondrial metabolism is required. Does NE stimulation induce glucose oxidation in addition to increased lactate formation under these conditions, and is this effect further enhanced in MBC-deficient BAT?

3. In Figure 6H, labeling in TCA cycle intermediates expressed as MPE% indicates extremely low labeling (under 1%). I may be misinterpreting the data, but the authors should explain how such a small contribution to the TCA cycle can explain a relatively large increase in respiration. Was the precursor pool (leucine, in this case) only partially labeled?

Reviewer #2:

This work provides a new understanding of how PGE2, a known pyrogen, impacts branched chain amino acid metabolism. There is little known about the metabolic adaptations that organisms undertake when a fever response is activated by PGE2. The authors used sophisticated in vivo approaches to administer PGE2 through ICV administration while simultaneously measuring body temperature. PGE2 treatment led to depletion of serum BCAA levels, while influx of BCAAs into BAT increased. Mitochondrial BCAA uptake via MBC is required for optimal thermogenesis induced by PGE2. The authors show that activated brown fat increases BCAA catabolism and provides carbons that provide substrate for the TCA cycle. The use of steady state and isotopic tracer analysis provides strong evidence for BCAA metabolism in fever-induced thermogenesis, which at the moment is poorly understood.

This is a well written manuscript that addresses the impact of PGE2 on BCAA metabolism. The authors provide a thorough analysis of PGE2 action in vivo. There are a few suggestions to help round out the paper and provide some clarity.

1. Does BCAA uptake in isolated mitochondria increase with PGE2 or CL treatment?

2. Where is the regulation of BCAA uptake? Is it by increasing uptake across plasma membrane or uptake in mitochondria?

3. Although loss of MBC decreases uptake of BCAA, there still remains substantial amount of Valine oxidation in knockout mice. Would that suggest that there is another mitochondrial BCAA transporter?

4. Does PGE2 increase UCP1 protein expression? A lot of the analysis includes changes in gene expression. However, protein expression has not been addressed.

Reviewer #3:

The authors set out to study the role of branched chain amiono acids (BCAA) into brown adipose tissue (BAT) during fever. BAT is a special type of fat that is important for non-shivering thermogenesis as a defence against a cold environment. Using BAT-specific knockout of BCAA and sophisticated models of fever, they show that the BCAA transporter MBC is important for the febrile response.

Yoneshiro et al. report that mitochondrial BCAA oxidation in brown adipose tissue (BAT) is significantly enhanced during fever. Genetic deletion of MBC in a BAT-specific manner reduces BAT function following intracerebroventricular PGE2 administration. The BCAA-induced increase in O2 consumption is blunted in MBC-null adipocytes.

This is a very interesting study and I have only one (rather minor) point that should be addressed:

Effect of BCAA on adipocytes: Figure 4f and 5a-d: The authors write "However, norepinephrine-induced thermogenesis was significantly enhanced when Leu was supplemented even in the presence of high glucose at 20 mM (Figure 5C). Importantly, this effect of Leu was not seen in the absence of MBC (Figure 5D)." This is confusing: In Figure 5C and D Val is shown. It would be interesting to directly compare the response (O2 consumption) of MBC-KO adipocytes to the three amino acids valine, leucine and isoleucine (with and without high glucose) administered during NE activation.

https://doi.org/10.7554/eLife.66865.sa1

Author response

Reviewer #1:

[…] 1. As the authors point out in the Discussion, the metabolic effects of BCAA degradation can include anaplerosis and/or the production of acetyl-CoA. This makes the respiration experiments in Figure 5 difficult to interpret, because Leu (used in Figure 5A,B) generates acetyl-CoA, whereas Val (Figure 5C,D) is anaplerotic. The effects on respiration may therefore differ. Can the authors harmonize these experiments by using the same amino acid for all conditions?

We appreciate the reviewer’s comment. We agree that this is an important point. To address the comment, we tested if supplementation of three BCAAs (Valine, Leucine, and Isoleucine) stimulates respiration in brown adipocytes. We found that all of them significantly augmented norepinephrine (NE)-stimulated respiration in an MBC-dependent fashion (see New Figure 5C).

The data suggest that the role of BCAA in thermogenic fat is likely more than merely a carbon source into the TCA cycle. This includes mitochondrial nitrogen supply, such as the synthesis of mitochondrial amino acids (Glu, Ala, Asp), given the fact that all the three BCAAs are nitrogen donors through the common deamination step by BCAT2. We discussed this point on Page 11 and 16.

2. The relevance of the enhanced glycolysis observed in Figure 5E is unclear. Converting glucose to lactate should not support thermogenesis if UCP1 and therefore oxidative mitochondrial metabolism is required. Does NE stimulation induce glucose oxidation in addition to increased lactate formation under these conditions, and is this effect further enhanced in MBC-deficient BAT?

We apologize for the confusion. It is well known that β-adrenergic receptor (β-AR) stimulation through norepinephrine (NE) induces both glucose oxidation and lactate production in brown adipocytes (Olsen et al., 2014, Ikeda et al., 2017). We measured lactate production as a readout to assess the fuel choice between glucose vs. BCAA in brown adipocytes following NE stimuli.

The data of higher lactate production in MBC KO cells relative to control cells (Figure 5F) suggest that MBC-deficient cells are limited to utilize glucose for NE-induced thermogenesis even in the presence of Leu. We discussed this point in our revised manuscript (Page 11).

3. In Figure 6H, labeling in TCA cycle intermediates expressed as MPE% indicates extremely low labeling (under 1%). I may be misinterpreting the data, but the authors should explain how such a small contribution to the TCA cycle can explain a relatively large increase in respiration. Was the precursor pool (leucine, in this case) only partially labeled?

Thank you for raising this issue. This is due to the fact that the present study employed a shorter labeling time (30 min) relative to our previous study that achieved ~20% MPE of TCA intermediates (Yoneshiro et al., 2019). In the present study, we aimed to determine how MBC loss affects the downstream pathway of Leu catabolism following NE stimulation. To this end, the cells were incubated with [13C]-Leu-containing medium for 30 min, and subsequently washed off (nonlabeled medium) and stimulated with NE for 1 hour (see Figure 6－figure supplement 1A). In contrast, our previous work (Yoneshiro et al., 2019) used a protocol in which cells were labeled for 1 hour during NE treatment. We discussed this point in our revised manuscript (Page 13).

Reviewer #2:

[…] This is a well written manuscript that addresses the impact of PGE2 on BCAA metabolism. The authors provide a thorough analysis of PGE2 action in vivo. There are a few suggestions to help round out the paper and provide some clarity.

1. Does BCAA uptake in isolated mitochondria increase with PGE2 or CL treatment?

We thank the reviewer for the constructive comments. Both CL treatment and PGE2 increased BCAA oxidation in the BAT (Figures 1F, 2B). Consistent with the data, we demonstrated that norepinephrine (NE) treatment increased the BCAA flux in the mitochondria (Figure 5A, 5C, and also in Yoneshiro et al., 2019). Hence, imported BCAAs to the isolated mitochondria would be rapidly oxidized (i.e., the mitochondrial BCAA content would be reduced) when stimulated by PGE2 or CL.

In fact, we found that isolated mitochondria from NE-stimulated brown adipocytes have lower [14C]-labeled Leu contents relative to non-stimulated brown adipocytes, due to high BCAA oxidation rate/flux (see Author response image 1). We would need to use a non-metabolized BCAA tracer to measure the accumulated Val contents in the mitochondria.

Author response image 1
Download asset Open asset
Effects of norepinephrine (NE) on mitochondrial BCAA content in brown adipocytes.

Differentiated brown adipocytes were treated with NE for 20 min and harvested to isolate mitochondria of brown adipocytes with shRNA knockdown of MBC (KD) or control cells. Subsequently, isolated mitochondria were incubated with [U-14C] Val at 37°C for 1 h. After washing with PBS 3 times, [U-14C] Val content in mitochondria was quantified by using a scintillation counter. n = 3/group. ANOVA with Tukey’s HSD test.

2. Where is the regulation of BCAA uptake? Is it by increasing uptake across plasma membrane or uptake in mitochondria?

This is an important point. Our recent study found that MBC overexpression increased the expression of SLC7A5 (LAT1), the plasma membrane transporter for neutral amino acids, including BCAAs (Walejko et al., 2021). The data suggest that mitochondrial BCAA uptake via MBC is linked to the plasma membrane uptake, although the underlying mechanism remains unknown.

We are also aware that BCAA oxidation is rapidly induced by norepinephrine or CL stimuli within a few minutes (see Figure 5A). It is possible that post-translational modifications, such as phosphorylation of MBC, may control MBC activity in a signal-dependent fashion. Thus, our future studies will investigate the signal-dependent post-translational modification of MBC.

We discussed this in our revised manuscript (Page 16).

3. Although loss of MBC decreases uptake of BCAA, there still remains substantial amount of Valine oxidation in knockout mice. Would that suggest that there is another mitochondrial BCAA transporter?

This is certainly possible. However, it is important to note that the BAT-specific KO mice lack MBC in brown adipocytes but not in other UCP1-negative cell types, such as endothelial cells, within the BAT. Thus, it is possible that Valine oxidation in KO mice may arise from UCP1negative cells in the BAT. We discussed this point on Page 8.

Another possibility is the contribution of keto-acids, e.g., α-ketoisovalerate (KIV). We previously showed that KIV uptake is not affected by MBC deletion (Yoneshiro et al., 2019). Although the expression of BCAT1 (the cytosolic form of BCAT) is low in BAT, oxidation of labeled KIV (deaminated from labeled Valine via BCAT1) could contribute to Valine oxidation.

4. Does PGE2 increase UCP1 protein expression? A lot of the analysis includes changes in gene expression. However, protein expression has not been addressed.

This is a valid point. Our new data showed that UCP1 protein expression was unchanged after 2 hours of an ICV administration of PGE2 (New Figure 1D).

Reviewer #3:

[…] This is a very interesting study and I have only one (rather minor) point that should be addressed:

Effect of BCAA on adipocytes: Figure 4f and 5a-d: The authors write "However, norepinephrine-induced thermogenesis was significantly enhanced when Leu was supplemented even in the presence of high glucose at 20 mM (Figure 5C). Importantly, this effect of Leu was not seen in the absence of MBC (Figure 5D)." This is confusing: In Figure 5C and D Val is shown. It would be interesting to directly compare the response (O2 consumption) of MBC-KO adipocytes to the three amino acids valine, leucine and isoleucine (with and without high glucose) administered during NE activation.

We appreciate the reviewer’s comment. We agree that this is an important point. To address the comment, we tested if supplementation of three BCAAs (Valine, Leucine, and Isoleucine) stimulates respiration in brown adipocytes. We found that all of them significantly augmented norepinephrine (NE)-stimulated respiration in an MBC-dependent manner (New Figure 5C).

The data suggest that the role of BCAA in thermogenic fat is more than merely a carbon source of fuel into the TCA cycle. This includes mitochondrial nitrogen supply, including the synthesis of mitochondrial amino acids (Glu, Ala, Asp), given the fact that all the three BCAAs are major nitrogen donors through the common deamination step by BCAT2. We discussed this point on Page 11 and 16.

References:

Ikeda, K., Kang, Q., Yoneshiro, T., Camporez, J. P., Maki, H., Homma, M., Shinoda, K., Chen, Y., Lu, X., Maretich, P., Tajima, K., Ajuwon, K. M., Soga, T. and Kajimura, S. 2017. UCP1-independent signaling involving SERCA2b-mediated calcium cycling regulates beige fat thermogenesis and systemic glucose homeostasis. Nat Med, 23, 1454-1465.

Olsen, J. M., Sato, M., Dallner, O. S., Sandstrom, A. L., Pisani, D. F., Chambard, J. C., Amri, E. Z., Hutchinson, D. S. and Bengtsson, T. 2014. Glucose uptake in brown fat cells is dependent on mTOR complex 2-promoted GLUT1 translocation. J Cell Biol, 207, 365-74.

Pedersen, H. K., Gudmundsdottir, V., Nielsen, H. B., Hyotylainen, T., Nielsen, T., Jensen, B. A., Forslund, K., Hildebrand, F., Prifti, E., Falony, G., Le Chatelier, E., Levenez, F., Dore, J., Mattila, I., Plichta, D. R., Poho, P., Hellgren, L. I., Arumugam, M., Sunagawa, S., Vieira-Silva, S., Jorgensen, T., Holm, J. B., Trost, K., Meta, H. I. T. C., Kristiansen, K., Brix, S., Raes, J., Wang, J., Hansen, T., Bork, P., Brunak, S., Oresic, M., Ehrlich, S. D. and Pedersen, O. 2016. Human gut microbes impact host serum metabolome and insulin sensitivity. Nature, 535, 376-81.

Walejko, J. M., Christopher, B. A., Crown, S. B., Zhang, G. F., Pickar-Oliver, A., Yoneshiro, T., Foster, M. W., Page, S., Van Vliet, S., Ilkayeva, O., Muehlbauer, M. J., Carson, M. W., Brozinick, J. T., Hammond, C. D., Gimeno, R.

E., Moseley, M. A., Kajimura, S., Gersbach, C. A., Newgard, C. B., White, P. J. and Mcgarrah, R. W. 2021. Branched-chain alpha-ketoacids are preferentially reaminated and activate protein synthesis in the heart. Nat Commun, 12, 1680.

Wolfe, R. R. 2017. Branched-chain amino acids and muscle protein synthesis in humans: myth or reality? J Int Soc Sports Nutr, 14, 30.

Yoneshiro, T., Wang, Q., Tajima, K., Matsushita, M., Maki, H., Igarashi, K., Dai, Z., White, P. J., Mcgarrah, R. W., Ilkayeva, O. R., Deleye, Y., Oguri, Y., Kuroda,

M., Ikeda, K., Li, H., Ueno, A., Ohishi, M., Ishikawa, T., Kim, K., Chen, Y., Sponton, C. H., Pradhan, R. N., Majd, H., Greiner, V. J., Yoneshiro, M., Brown, Z., Chondronikola, M., Takahashi, H., Goto, T., Kawada, T., Sidossis, L., Szoka, F. C., Mcmanus, M. T., Saito, M., Soga, T. and Kajimura, S. 2019. BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature, 572, 614-619.

https://doi.org/10.7554/eLife.66865.sa2

Article and author information

Author details

  1. Takeshi Yoneshiro

    1. Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, United States
    2. Division of Metabolic Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan
    Contribution
    Data curation, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing - original draft
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-5298-5831

  2. Naoya Kataoka

    Department of Integrative Physiology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Contribution
    Resources, Data curation, Validation, Investigation, Methodology
    Competing interests
    No competing interests declared

  3. Jacquelyn M Walejko

    Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States
    Contribution
    Data curation, Formal analysis, Investigation
    Competing interests
    No competing interests declared

  4. Kenji Ikeda

    1. Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, United States
    2. Department of Molecular Endocrinology and Metabolism, Tokyo Medical and Dental University, Tokyo, Japan
    Contribution
    Resources, Investigation
    Competing interests
    No competing interests declared

  5. Zachary Brown

    Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, United States
    Contribution
    Resources, Validation
    Competing interests
    No competing interests declared

  6. Momoko Yoneshiro

    Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, United States
    Contribution
    Resources, Validation
    Competing interests
    No competing interests declared

  7. Scott B Crown

    Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States
    Contribution
    Data curation, Methodology
    Competing interests
    No competing interests declared

  8. Tsuyoshi Osawa

    Division of Integrative Nutriomics and Oncology, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan
    Contribution
    Resources
    Competing interests
    No competing interests declared

  9. Juro Sakai

    1. Division of Metabolic Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan
    2. Division of Molecular Physiology and Metabolism, Tohoku University Graduate School of Medicine, Sendai, Japan
    Contribution
    Resources
    Competing interests
    No competing interests declared

  10. Robert W McGarrah

    1. Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States
    2. Department of Medicine, Division of Cardiology, Duke University School of Medicine, Durham, United States
    Contribution
    Data curation, Formal analysis, Supervision
    Competing interests
    No competing interests declared

  11. Phillip J White

    1. Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States
    2. Department of Medicine, Division of EndocrinologyMetabolism and Nutrition, Duke University School of Medicine, Durham, United States
    Contribution
    Data curation, Formal analysis, Supervision
    Competing interests
    No competing interests declared

  12. Kazuhiro Nakamura

    Department of Integrative Physiology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Contribution
    Data curation, Formal analysis, Supervision, Validation, Investigation
    Competing interests
    No competing interests declared

  13. Shingo Kajimura

    1. Diabetes Center and Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, United States
    2. Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Durham, United States
    Contribution
    Conceptualization, Formal analysis, Supervision, Funding acquisition, Writing - original draft, Project administration
    For correspondence
    skajimur@bidmc.harvard.edu
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0672-5910

Funding

National Institute of Diabetes and Digestive and Kidney Diseases (DK097441)

  • Shingo Kajimura

National Institute of Diabetes and Digestive and Kidney Diseases (DK126160)

  • Shingo Kajimura

National Institute of Diabetes and Digestive and Kidney Diseases (DK125281)

  • Shingo Kajimura

National Institute of Diabetes and Digestive and Kidney Diseases (DK127575)

  • Shingo Kajimura

Edward Mallinckrodt, Jr. Foundation

  • Shingo Kajimura

National Heart and Lung Institute (5K08HL13527)

  • Robert W McGarrah

National Heart and Lung Institute (F32HL137398)

  • Scott B Crown

American Diabetes Association (1-16-INI-17)

  • Phillip J White

Japan Society for the Promotion of Science (19K06954)

  • Kazuhiro Nakamura

Japan Society for the Promotion of Science (15H05932)

  • Naoya Kataoka

Japan Society for the Promotion of Science (15K21744)

  • Naoya Kataoka

Japan Society for the Promotion of Science (20H03418)

  • Naoya Kataoka

AMED (JP21gm5010002s0305)

  • Kazuhiro Nakamura

AMED (JPMJMS2023)

  • Kazuhiro Nakamura

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank Olga Byakina and Yasuo Oguri for their technical support. This work was supported by the NIH (DK097441, DK126160, DK125281, and DK127575 to SK, 5K08HL135275 to RWM, and F32HL137398 to SBC), an American Diabetes Association Pathways to Stop Diabetes Initiator Award (# 1-16-INI-17) to PJW, the Edward Mallinckrodt, Jr. Foundation to SK, MEXT KAKENHI (15H05932, 15K21744, and 20H03418 to KN and 19K06954 to NK), AMED (JP21gm5010002s0305) to KN, and JST Moonshot R&D (JPMJMS2023) to KN. TY was supported by the JSPS Fellowships and the Uehara Memorial Foundation, and JMW was supported by Cardiovascular-Metabolic Fellowship (#1-21-CMF-005).

Ethics

Animal experimentation: All the animal experiments were performed following the guidelines by the UCSF Institutional Animal Care and Use Committee or by the Nagoya University Animal Experiment Committee. The protocols were approved by the committees by the Committee on the Ethics of Animal Experiments of UCSF (AN165833) and Nagoya University. All surgery was performed under anesthesia, and every effort was made to minimize suffering.

Senior Editor

  1. David E James, The University of Sydney, Australia

Reviewing Editor

  1. Ralph J DeBerardinis, UT Southwestern Medical Center, United States

Reviewer

  1. Ralph J DeBerardinis, UT Southwestern Medical Center, United States

Publication history

  1. Received: January 25, 2021
  2. Accepted: May 2, 2021
  3. Accepted Manuscript published: May 4, 2021 (version 1)
  4. Version of Record published: May 20, 2021 (version 2)

Copyright

© 2021, Yoneshiro et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Takeshi Yoneshiro
  2. Naoya Kataoka
  3. Jacquelyn M Walejko
  4. Kenji Ikeda
  5. Zachary Brown
  6. Momoko Yoneshiro
  7. Scott B Crown
  8. Tsuyoshi Osawa
  9. Juro Sakai
  10. Robert W McGarrah
  11. Phillip J White
  12. Kazuhiro Nakamura
  13. Shingo Kajimura
(2021)
Metabolic flexibility via mitochondrial BCAA carrier SLC25A44 is required for optimal fever
eLife 10:e66865.
https://doi.org/10.7554/eLife.66865

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