ACE2 pathway regulates thermogenesis and energy metabolism
Abstract
Identification of key regulators of energy homeostasis holds important therapeutic promise for metabolic disorders, such as obesity and diabetes. ACE2 cleaves angiotensin II (Ang II) to generate Ang-(1-7) which acts mainly through the Mas1 receptor. Here, we identify ACE2 pathway as a critical regulator in the maintenance of thermogenesis and energy expenditure. We found that ACE2 is highly expressed in brown adipose tissue (BAT) and that cold stimulation increases ACE2 and Ang-(1-7) levels in BAT and serum. Ace2 knockout mice (Ace2-/y) and Mas1 knockout mice (Mas1-/-) displayed impaired thermogenesis. Mice transplanted with brown adipose tissue from Mas1-/- display metabolic abnormalities consistent with those seen in the Ace2 and Mas1 knockout mice. In contrast, impaired thermogenesis of Leprdb/db obese diabetic mice and high-fat diet-induced obese mice were ameliorated by overexpression of Ace2 or continuous infusion of Ang-(1-7). Activation of ACE2 pathway was associated with improvement of metabolic parameters, including blood glucose, lipids, and energy expenditure in multiple animal models. Consistently, ACE2 pathway remarkably enhanced the browning of white adipose tissue. Mechanistically, we showed that ACE2 pathway activated Akt/FoxO1 and PKA pathway, leading to induction of UCP1 and activation of mitochondrial function. Our data propose that adaptive thermogenesis requires regulation of ACE2 pathway and highlight novel potential therapeutic targets for the treatment of metabolic disorders.
Editor's evaluation
Authors have found that ACE2 is highly expressed in brown adipose tissue (BAT), indicating ACE2 pathway as a critical regulator in the maintenance of thermogenesis and energy expenditure. Identifying new regulators of energy homeostasis authors have shed light on novel potential therapeutic targets for the treatment of metabolic disorders.
https://doi.org/10.7554/eLife.72266.sa0Introduction
Energy imbalance and the associated metabolic syndromes have become a worldwide public health problem. Thus, identifying factors that can stimulate energy expenditure is instrumental to the development of therapeutics to reduce obesity associated disorders that affect over 10% of the world population (Dong et al., 2018). In the renin-angiotensin system (RAS), angiotensin-converting enzyme 2 (ACE2) cleaves angiotensin II (Ang II) to generate angiotensin-(1-7) (Ang-(1-7)). Ang-(1-7) is a heptapeptide hormone which acts mainly through G-protein-coupled receptor Mas1 (Santos et al., 2003). ACE2-Ang-(1-7)-Mas1 pathway works as a negative regulator of ACE-Ang II pathway in multiple disease states (Clarke and Turner, 2012).
Our group focused on ACE2 originated from concerns of severe acute respiratory syndrome (SARS) in 2003. Ambient hyperglycemia occurred very early in SARS patients and was an independent predictor for death and morbidity in SARS patients (Yang et al., 2006). Interestingly, ACE2 is the functional receptor for SARS coronavirus (Lavoie and Sigmund, 2003). We reported that Ace2 knockout (Ace2-/y) mice exhibited progressive impairments in glucose tolerance indicating that ACE2 is a potential new target for the treatment of type 2 diabetes (Niu et al., 2008). In addition, we have demonstrated that ACE2 regulates mitochondrial function in pancreatic β-cells, inhibits hepatic insulin resistance, ameliorates hepatic steatosis, and improves glucose uptake in adipocytes (Cao et al., 2019; Cao et al., 2016; Cao et al., 2014; Liu et al., 2012a; Song et al., 2020; Yang et al., 2018). These findings support the hypothesis that the ACE2-Ang-(1-7)-Mas1 axis may have protective effects on metabolic syndrome.
In this study, we reported the effects of ACE2 pathway on regulating thermogenesis and energy metabolism via modulating mitochondrial function. We found that Ace2-/y and Mas1 knockout (Mas1-/-) mice are cold intolerance. We provided compelling genetic, metabolic, physiological, histological, cellular, and molecular evidence to demonstrate that ACE2 pathway is a critical regulator in the maintenance of energy expenditure. This pathway regulates function of brown adipose tissue (BAT) and systemic energy metabolism. Mechanistically, ACE2 pathway activates both Akt/FoxO1 signaling and PKA signaling, leading to induction of uncoupling protein-1 (UCP1) and activation of mitochondrial function. Therefore, ACE2 pathway is a potential treatment target for metabolic disorders including diabetes, obesity, and even cardiovascular diseases.
Results
Acute cold exposure increases components of ACE2 pathway
The major tissue of the body where energy is converted into the form of heat to maintain the body temperature is BAT. We found both mRNA level and protein level of Ace2 and Mas1 in BAT were obviously higher than the ones in subcutaneous white adipose tissue (scWAT) and epididymal white adipose tissue (eWAT) in mice (Figure 1A and B). Acute cold exposure caused a significant up-regulation of ACE2 protein expression in BAT (Figure 1C). Meanwhile, Ace2 mRNA levels in BAT, scWAT and eWAT, and Mas1 mRNA levels in BAT and eWAT were increased after exposed to 4 °C for 48 hr (Figure 1D and E). ACE2 and Ang-(1-7) were also marginally increased in serum upon cold challenge (Figure 1F and G). These results demonstrated a selective induction of ACE2 pathway in thermogenic adipose depots (BAT and scWAT) in response to cold environment.
ACE2 promotes thermogenesis and energy metabolism
To explore the physiological roles of ACE2 in cold-induced adaptive thermogenesis, we used the HFD-induced Ace2-/y mice. ACE2 is essential for expression of neutral amino acid transporters in the gut (Hashimoto et al., 2012). This is consistent with our observation that Ace2-/y mice fed an HFD displayed significantly decreased weight compared to wild-type (WT) mice (Figure 2A). Serum Ang-(1-7) levels were decreased in the Ace2-/y mice (Figure 2B). Consistent with previous studies (Cao et al., 2014; Liu et al., 2012a; Niu et al., 2008; Shi et al., 2018; Zhang et al., 2016), Ace2-/y mice had an impaired glucose tolerance and abnormal lipid profiles (Figure 2—figure supplement 1A-C).
A key factor for controlling energy homoeostasis is the balance between caloric intake and energy expenditure. Thus, we measured energy expenditure using a comprehensive laboratory animal monitoring system (CLAMS). We observed a decreased oxygen consumption (VO2), carbon dioxide release (VCO2) and energy expenditure (EE) in Ace2-/y mice (Figure 2C, D and E), without observable changes in food and/or water intake as well as physical activity, compared to the WT mice (Figure 2—figure supplement 1D-F).
To further examine the differences in energy expenditure among these animals, we performed a cold tolerance test in order to gauge adaptive thermogenesis. Ace2-/y mice had lower thermogenesis than the WT mice in a cold environment (4 °C) (Figure 2—figure supplement 1G). To explore the source of thermogenesis, we analyzed the non-shivering thermogenesis (NST) of Ace2-/y mice in thermoneutral condition (30 °C), ambient temperature (22 °C) and acute cold (4 °C) for 8 hr. Ace2-/y mice had lower thermogenesis than the WT mice in either 22 °C or 4 °C (Figure 2F). This temperature difference was monitored by an infrared camera at 4 °C (Figure 2G).
To investigate whether ACE2-induced thermogenesis was related to BAT function, we performed the Positron emission tomography–computed tomography (PET-CT) analysis and the results showed a higher PET-CT signal in BAT of the HFD-induced WT mice than Ace2-/y mice (Figure 2H). As expected, BAT in Ace2-/y mice displayed larger lipid droplets but reduced multilocular structures compared to the WT mice, and reduced UCP1 expression (Figure 2I).
To evaluate the significance of cold-induced ACE2 for thermogenic function of BAT, the expression levels of a network of genes and proteins controlling energy expenditure and thermogenic programming were measured. Protein levels (UCP1, PGC1α, and ATP5A) (Figure 2J) and mRNA levels (Ucp1, Prmd16, and Pparg (Figure 2—figure supplement 1H)) in BAT from Ace2-/y were obviously decreased.
To validate the above-mentioned change of thermogenesis of BAT was cell autonomous, primary brown adipocytes from Ace2-/y mice was fractionated and differentiated in vitro. Notably, the protein and mRNA expression of known BAT markers were robustly decreased in Ace2-deficient primary brown adipocytes (Figure 2K, Figure 2—figure supplement 1I). Immunohistochemistry was applied to study the level of UCP1 in primary brown adipocytes differentiated from the BAT of the Ace2-/y mice. The result showed the UCP1 expression was reduced in the Ace2 deficiency primary brown adipocytes (Figure 2L). More importantly, the oxygen consumption rate (OCR) was significantly decreased in Ace2-deficient primary brown adipocytes (Figure 2M).
As a complementary approach to the KO mouse models, we carried out gain-of-function studies using Ace2 over expression in obese diabetic Leprdb/db mice. One week following adenovirus-induced Ace2 over-expression (Ad-Ace2) by tail vein injection in the Leprdb/db mice, both ACE2 (Figure 3—figure supplement 1A) in BAT and circulating Ang-(1-7) (Figure 3A) were increased. Consistent with our previous study, the Ad-Ace2-treated mice exhibited an improved metabolic profile as indicated by the significant alleviation of glucose intolerance (Figure 3—figure supplement 1B). Notably, although no observable change on the body weight was observed in the two groups (Figure 3B), serum triglyceride levels decreased in the Ad-Ace2-treated mice (Figure 3—figure supplement 1C), as well as a minor change in serum cholesterol levels (Figure 3—figure supplement 1D).
Notably, the Ad-Ace2-treated Leprdb/db mice had increased energy expenditure (VO2, VCO2 and EE) (Figure 3C–E). There was no obvious change in food and/or water intake as well as physical activity (Figure 3—figure supplement 1E-G).
We measured rectal temperature and infrared thermal imaging in the Leprdb/db mice that BAT activity was defective as same as the ones in previous observations (Trayhurn and Wusteman, 1990; Zhang et al., 2014). The results showed that the thermogenesis of the Leprdb/db mice was severely impaired (Figure 3—figure supplement 1H, I). As expected, the Ad-Ace2 treated Leprdb/db mice and HFD-induced obese mice exhibited better thermogenesis than the control mice in ambient temperature (22 °C) and acute cold (4 °C) conditions (Figure 3F and G, Figure 3—figure supplement 1J,K). Accordingly, PET-CT result showed that BAT was activated in the Ad-Ace2-treated Leprdb/db mice (Figure 3H). Moreover, BAT in the Ad-Ace2-treated Leprdb/db mice had smaller lipid droplets but increased multi-locular structures, and had increased UCP1 expression compared with the control group (Figure 3I).
The protein levels of UCP1, ATP5A and UQCRC2 were significantly increased in the BAT from the Ad-Ace2 treated mice (Figure 3J). Consistently, the mRNA levels, including Ucp1, ATP synthase F1 subunit beta (Atp5b), Cox8b, Cox7a, fatty acid binding protein 4 (Fabp4), Cpt1a, Prdm16, Ppargc1a and Ppargc1b, were increased in the BAT from the Ad-Ace2-treated Leprdb/db mice (Figure 3K). Taken together, these results indicated that ACE2 effectively regulated the mitochondrial biogenesis and respiratory function in brown adipocytes.
Ang-(1-7) promotes thermogenesis and energy metabolism
To explore the direct physiological roles of Ang-(1-7) in cold-induced adaptive thermogenesis, Ang-(1-7) administration by subcutaneous implantation of micro-osmotic pumps in the Leprdb/db and the HFD-induced obese mice were employed. Serum Ang-(1-7) was increased in Ang-(1-7)-treated mice (Figure 4—figure supplement 1A). There are no significant differences in body weight between the Ang-(1-7)-treated Leprdb/db mice and the Leprdb/db control mice (Figure 4A); however, Ang-(1-7)-treated Leprdb/db mice has an improved glucose tolerance ability (Figure 4—figure supplement 1B) and better lipid profiles (Figure 4—figure supplement 1C, D). The Ang-(1-7)-treated HFD-induced obese mice displayed a lower body weight compared to the control (Figure 4B).
Notably, the Ang-(1-7) treated Leprdb/db mice had increased energy expenditure (VO2, VCO2, and EE) (Figure 4C–E) without any changes in food and/or water intake as well as physical activity (Figure 4—figure supplement 1E-G). Moreover, the Ang-(1-7) treated Leprdb/db and the HFD-induced obese mice were better able to defend their body temperature during environmental cold (22 °C) and acute cold stress (4 °C) compared to the control (Figure 4F–H, Figure 4—figure supplement 1H). Meanwhile, the Ang-(1-7)-treated Leprdb/db mice had increased multi-locular structures but smaller lipid droplets, and increased UCP1 expression comparing to the control group (Figure 4I). Accordingly, the Ang-(1-7)-treated Leprdb/db and the HFD-induced obese mice showed more 18F-FDG uptake in the BAT than the control mice recorded by PET-CT (Figure 4J and K).
The protein levels of UCP1 and PGC1α were significantly induced in the BAT from the Ang-(1-7) treated Leprdb/db and the HFD-induced obese mice (Figure 4L and M). The mRNA levels, including Ucp1, Ppargc1a, Cidea, Atp5b, Cox4, Cox8b, Cox7a, Mcad, and Fabp2, were increased in the BAT from the Ang-(1-7)-treated Leprdb/db mice (Figure 4—figure supplement 1I).
To sum up, our results suggested that the enhanced thermogenesis effect in the Ad-Ace2 and Ang-(1-7) treated mice is caused by the increment of Ang-(1-7) levels, which demonstrates that Ang-(1-7) is crucial to the maintenance of thermogenesis.
Ablation of Mas1 impairs thermogenesis in brown adipose tissue
Since the Ang-(1-7), produced by ACE2, realized the function through the Mas1 receptor, these results above prompted us to hypothesize that the Mas1 receptor determines the effect of Ang-(1-7) in brown adipose tissue. Firstly, the HFD-induced Mas1-/-mice (low Ang-(1-7) action model) were used to assess the therapeutic effects (interventional effects) of Mas1 on energy metabolism. Although serum Ang-(1-7) levels were increased, the Mas1-/-mice had an impaired glucose tolerance, abnormal lipid profiles (Figure 5A, Figure 5—figure supplement 1A-C), and significantly increased body weight compared to the WT mice (Figure 5B). Meanwhile, the Mas1-/- mice exhibited decreased oxygen consumption (VO2) (Figure 5—figure supplement 1D) without any changes in food and/or water intake as well as physical activity (Figure 5—figure supplement 1E-G). Moreover, the Mas1-/- mice had lower thermogenesis than the WT mice in either 22 °C or 4 °C (Figure 5C, D and F). PET-CT analysis illustrated that the Mas1-/- mice has less 18F-FDG uptake in BAT than the WT mice (Figure 5E). Consistently, the Mas1-/- mice displayed larger lipid droplets and reduced multilocular structures, and had reduced UCP1 expression compared with the WT mice (Figure 5G). Nevertheless, deletion of Mas1 resulted in a striking repression of BAT thermogenic protein (UCP-1, UQCRC2, and SDHB) (Figure 5H) and genes (e.g. Ucp1, Prmd16, Ppargc1a, Ppargc1b, Atp5b, Cox7a, and Cpt1a) (Figure 5I).
To investigate the role of the Mas1 receptor in BAT, we generated BAT-specific Mas1 knockout mice (Mas1-/- BAT transplanted mice). According to the previous studies (Liu et al., 2013; Yuan et al., 2016), firstly, BAT of the C57B/L6 recipient mice was removed from the interscapular region. Then, the BAT, which dissected from strain-, sex-, and age-matched Mas1-/- donor mice, was subcutaneously transplanted into the dorsal interscapular region of the C57B/L6 recipient mice (WT + Mas1-/--BAT). As controls, C57B/L6-recipient mice transplanted with C57B/L6 BAT (WT + WT BAT) and C57B/L6 epididymal white adipose tissue (eWAT) (WT + WT eWAT) were used as positive control and negative control, respectively. After the transplantation, the recipient mice were fed by HFD for 10 weeks.
Interestingly, compared with the WT + WT BAT control mice, the WT + Mas1-/--BAT mice showed greatly impaired HFD-induced insulin resistance. There is no significant difference between the WT + Mas1-/--BAT mice and the WT + WT eWAT mice in intraperitoneal glucose tolerance test (GTT) and the insulin tolerance test (ITT) (Figure 5J and K). Notably, Mas1-/-BAT transplantation also strikingly induced HFD-induced weight gain in the WT + Mas1-/--BAT mice compared with the WT + WT BAT control mice (Figure 5L).
More importantly, compared to the WT + WT BAT control mice, the WT + Mas1-/--BAT mice had decreased oxygen consumption (VO2), carbon dioxide release (VCO2), and energy expenditure (EE) (Figure 5M–O), along with normal food and/or water intake as well as physical activity (Figure 5—figure supplement 1H-J). Taken together, these results demonstrate that the Mas1 receptor can directly induce thermogenic program in brown adipose tissues.
ACE2 pathway induces white fat browning and thermogenesis
Next, we investigated the impact of ACE2/Ang-(1-7) on the process of browning of WAT, a prominent feature in subcutaneous white adipose tissue (scWAT). Histological examination of scWAT from the Ad-Ace2-treated Leprdb/db obese mice showed a profound morphological transformation toward a BAT-like phenotype (smaller adipocytes with multiple lipid droplets) compared with the control (Figure 6A). Meanwhile, markers of brown adipocytes, such as Ucp1, were significantly increased in scWAT of the Ad-Ace2-treated Leprdb/db mice. A much greater induction of transcription factors, including Prmd16, Ppargc1a and Ppargc1b, occurred in the scWAT of the Ad-Ace2-treated group (Figure 6B). As expected, the Ang-(1-7) treated Leprdb/db mice had a similar browning effect as the Ad-Ace2-treated Leprdb/db mice in scWAT. Morphological brown-like adipocyte and thermogenic gene expression levels slight increasement were observed in the scWAT after Ang-(1-7) treatment (Figure 6C and D).
These alterations were restricted to scWAT, but not to epididymal white adipose tissue (eWAT). As shown in Figure 6E, the morphology and size of eWAT in the Ad-Ace2-treated Leprdb/db mice are same compared to the control (Figure 6E). Meanwhile, no significant increase in the thermogenic gene expression levels in the eWAT of the Ad-Ace2-treated Leprdb/db mice was found (Figure 6F).
ACE2 pathway enhances thermogenesis via Akt and PKA signaling
We further investigated the molecular mechanisms through which ACE2 pathway regulates BAT. Firstly, we performed RNA-seq analysis on BAT isolated from the WT and the Ace2 KO mice. Notable differences between the two are displayed as 3D-PCA analysis and heat map (Figure 7—figure supplement 1A, B). Consistent with the RT-PCR results of BAT in the Ace2 KO mice, genetic deficiency of Ace2 significantly altered expression of genes involved in fatty acid biosynthesis, lipid catabolism, lipid biosynthesis, fatty acid beta-oxidation, and cholesterol biosynthesis in the BAT of the Ace2 KO mice (Figure 7—figure supplement 1C).
Interestingly, we found that the expression level of Akt associated genes were significantly decreased in the Ace2 KO mice compared with the WT mice (Figure 7—figure supplement 1D). The phosphorylation levels of Akt at residues Thr308 was significantly inhibited in BAT of the Ace2 KO mice (Figure 7A). Furthermore, the phosphorylation levels of Akt were dramatically increased in BAT of the Ad-Ace2-treated mice (Figure 7B).
These results prompted us to consider whether ACE2 pathway regulates the function of BAT via Akt signaling. Thus, we treated primary brown adipocytes which isolated from mice with Ang-(1-7). We found phosphorylation of Akt was activated by Ang-(1-7), accompanied by UCP1 up-regulation and forkhead box-containing protein O subfamily-1 (FoxO1) phosphorylation (Figure 7C). MK2206, an Akt inhibitor (Chorner and Moorehead, 2018; Matsuzaki et al., 2018), suppressed Ang-(1-7)-induced UCP1 up-regulation and FoxO1 phosphorylation (Figure 7C). Compared to Ang-(1-7)-treated primary brown adipocytes cells, MK2206 down-regulated the mRNA levels of Ucp1, Ppargc1a, Cidea, Atp5b, Fabp4, and Cpt1a genes (Figure 7D). More importantly, Ang-(1-7)-treated primary brown adipocytes exhibited higher OCR, and MK2206 inhibited OCR in the Ang-(1-7) treated primary brown adipocytes (Figure 7E). Accordingly, the Ace2-overexpressing primary brown adipocytes cells showed a similar result. MK2206 suppressed ACE2 induced up-regulation of protein (UCP1 and phosphorylated FoxO1) (Figure 7—figure supplement 2A) and mRNA (Ucp1 and Cpt1a) (Figure 7—figure supplement 2B), as well as action on OCR (Figure 7—figure supplement 2C). These results suggest that the Akt signaling are required for the thermogenic activity of ACE2 pathway.
After the determination that ACE2 pathway regulates adaptive thermogenesis through the Akt signaling, we paid attention on whether this program could still be provoked by protein kinase A (PKA) signaling, a pathway known to be involved in the canonical thermogenic activation of fat cells. Interestingly, we found that the phosphorylation level of PKA was significantly inhibited in BAT of the Ace2 KO mice (Figure 7F). Similar results appeared in the Mas1 KO mice (Figure 7—figure supplement 2D). However, the phosphorylation level of PKA was increased in BAT of the Ad-Ace2-treated Leprdb/db mice (Figure 7G).
To further elucidate the study on the mechanism of Ang-(1-7)-induced PKA signaling, we administrated Ang-(1-7)-treated primary brown adipocytes with PKA and adenylylcyclase inhibitors, simultaneously. Firstly, the Ang-(1-7)-induced PKA signaling was validated in primary brown adipocytes (Figure 7—figure supplement 2E). However, H89, a PKA inhibitor, significantly blunted the Ang-(1-7)-induced mRNA levels (Ucp1, Cidea, and Fabp4) (Figure 7H) and protein levels (UCP1 and PGC1α) (Figure 7I). Similar effects were observed by using SQ-22536, an adenylylcyclase inhibitor on the formation of intracellular cAMP (Figure 7H,I). As expected, the Ang-(1-7)-treated primary brown adipocytes exhibited higher OCR, and H89 inhibited OCR in the Ang-(1-7)-treated primary brown adipocytes (Figure 7J). H89 also suppressed ACE2-induced maximal respiration (Figure 7—figure supplement 2F). Our results thus strongly suggest that the PKA signaling is important for the thermogenic activity of ACE2 pathway.
Combine with the above result, these data indicated that Ang-(1-7) treatment induced respiration at least partly through Akt and PKA signaling pathway. Notably, treatment with PKA inhibitors on non-Ang-(1-7) stimulated cells results in very little change in OCR, whereas treatment on Ang-(1-7) stimulated cells results in reversion to normal OCR levels (Figure 7J). In contrast, treatment of non-Ang-(1-7) stimulated cells with AKT inhibitors led to an equivalent level of decrease in OCR as in Ang-(1-7)-treated cells (Figure 7E), suggesting that AKT inhibition may generically decrease OCR in adipocytes, whereas inhibiting PKA only affects the OCR of Ang-(1-7)-treated cells. PKA is more likely responsible in the changes in mitochondrial activity due to Ang-(1-7) stimulation than AKT signaling. More importantly, our data showed that co-treatment with Akt and PKA inhibitors have an additive effect in Ace2-overexpressing primary brown adipocytes cells (Figure 7—figure supplement 2G).
Furthermore, in Ang-(1-7)-treated primary brown adipocytes, there is no significant difference between A779 and PKA/Akt inhibitor treatment on OCR (Figure 7—figure supplement 2H). This data indicated that A779 treatment plays similar effect to PKA/Akt inhibitor on mitochondrial respiration in Ang-(1-7) treated cells.
Discussion
RAS is classically known to regulate blood pressure and maintain water and electrolyte balance. It also plays as a crucial role in metabolic disorders, such as obesity and insulin resistance (Das, 2016). Comprehensive understanding of the complexly biological function of the RAS remains a major biomedical challenge. Recently, a research group separately reported that ACE2 and Ang-(1-7) exert anti-obesity effect by BAT in HFD-induced obesity mice (Kawabe et al., 2019; Morimoto et al., 2018). In ACE2 pathway, ACE2, Ang-(1-7), and Mas1 receptor interact and antagonize each other’s actions. As these two studies only used gain-of-function approaches, they cannot clarify the specific physiological role of ACE2-Ang1-7-Mas1 axis in the thermogenesis brown adipose tissue. Therefore, it is critically important and urgent to systematically analyze the function of these three elements using reverse genetics approaches.
In our study, we used seven mice models, Ace2 KO mice, Ad-Ace2 Leprdb/db and HFD mice, Ang-(1-7) treated Leprdb/db and HFD mice, Mas1 KO mice and BAT-specific Mas1 knockout mice (Mas1-/- BAT transplanted mice), respectively. Based on a series of functional assays in these mouse models and primary brown adipocytes, we effectively confirmed that the ACE2 pathway regulates glucose and lipid homeostasis. Furthermore, ACE2 pathway maintains thermogenesis and systemic energy metabolism. Molecular analyses, including the use of several inhibitors of Akt and PKA, demonstrate that the effects of ACE2 pathway on brown adipocytes are mediated by both the Akt signaling and the PKA signaling, resulting in the activation of PGC1α, followed by activation of UCP1 (Figure 7K). These findings significantly expand our understanding of the biological function of RAS. Furthermore, our results propose a new concept that the ACE2 pathway can improve obesity and the associated metabolic disorders.
BAT, which utilizes glucose and fatty acids for thermogenesis, contains large number of mitochondria and promotes thermogenesis by mitochondrial respiration through UCP1. BAT-specific UCP1, localized in the inner mitochondrial membrane, plays a fundamental role in thermogenesis. In response to stimulation, activation of PGC1α up-regulates the expression of BAT-specific UCP1, which dissipates the proton motive force across the inner mitochondrial membranes, and consequentially producing ATP (Sambeat et al., 2016; Schreiber et al., 2017). On the other hand, PGC1α induces the acquisition of BAT features, including the expression of mitochondria and fatty acid-oxidation and thermogenic genes (Puigserver et al., 1998; Tiraby et al., 2003). We found that the mRNA levels of Ucp1, Ppargc1a, mitochondrial program and fatty acid oxidation related genes (Ppargc1b, Atp5b, Cox7a, Cox8b, Fabp4, and Cpt1a) were up-regulated in the Ace2 overexpression and the Ang-(1-7)-treated Leprdb/db mice, whereas down-regulated in the Ace2 KO or the Mas1 KO mice. These results supported that PGC1α and UCP1 might be critical for the effects of ACE2 pathway on thermogenesis.
We also investigated the underlying mechanisms of ACE2 pathway on the regulation of BAT via the Akt signaling and the PKA signaling (Figure 7K).
First, we verified the Akt signaling in the downstream of ACE2 pathway. Akt has a critical function in cell survival and energy balance. Multiple pieces of evidence show that activation of PI3K is followed by the activation of Akt, which in turn triggers a complex cascade of events that include the inhibition of FoxO1 transcription factors and thus the activation of Ucp1 and its transcriptional regulator PGC1α (Nakae et al., 2008; Ortega-Molina et al., 2012). In human and 3T3-L1 preadipocytes, Ang-(1-7)-Mas1 signaling promotes adipogenesis via activation of PI3K-Akt signaling (Than et al., 2013). AT2R activation induces white adipocyte browning by increasing PPARγ expression, at least in part, via PI3K-Akt signaling pathways (Than et al., 2017). We previously reported that ACE2 and Ang-(1-7) can activate Akt signaling to ameliorate hepatic steatosis (Cao et al., 2016; Cao et al., 2014). In the present study, the Ace2 KO and the Mas1 KO mice displayed a strong decrease in Akt S308 phosphorylation in BAT. The Ace2 over-expression or the Ang-(1-7) treatment activated Akt S308 phosphorylation in BAT. Furthermore, the effect of ACE2-Ang-(1-7) on primary brown adipocytes can be attenuated by Akt inhibitor. These results suggest that the Akt signaling might also play a role in ACE2 pathway related regulation of BAT function.
Second, we verified the PKA signaling in the downstream of ACE2 pathway. The Mas1 receptor was shown to constitutively couple to Gαs, including Gαi, Gαq, and Gα12/13proteins (Dias-Peixoto et al., 2008; Gomes et al., 2012; Tirupula et al., 2014). In the kidney, Ang-(1-7) treatment increased cAMP levels and activated PKA through Gαs activation by the Mas1 receptor (Liu et al., 2012b; Magaldi et al., 2003). Ang-(1-7) regulates insulin secretion through a Mas1-dependent cAMP signaling pathway (Sahr et al., 2016). It is well known that norepinephrine released from the sympathetic nerves is a powerful stimulator of BAT. Norepinephrine activates BAT thermogenic program via PKA signaling, followed by the UCP1-mediated proton uncoupling (Su et al., 2017). In this study, the PKA signaling in BAT was changed significantly by ACE2 pathway in mice model. In addition, the effect of ACE2 pathway on primary brown adipocytes can be depressed by cAMP and PKA inhibitor.
Previously, we demonstrate that the ACE2 pathway is involved in the regulation of glucose and lipid homeostasis with limited understanding of the underlying mechanisms (Cao et al., 2014; Liu et al., 2012a; Niu et al., 2008; Shi et al., 2018; Zhang et al., 2016). Here, for the first time, we provide evidence that the alteration in glucose and lipid homeostasis is associated with the change in maintaining brown adipocyte function for the facilitation of energy expenditure. In summary, the ACE2 pathway regulates BAT function and systemic energy metabolisms which is a potential treatment target for metabolic disorders including metabolic syndrome, diabetes, dyslipidemia, and fatty liver.
Materials and methods
Mice
Obese BKS-db (Leprdb/db) male mice, wild-type mice and Mas1 KO mice were purchased from Nanjing Biological Medicine Research Institute, Nanjing University, China. Male C57BL/6 J mice were purchased from Vital River Laboratory Animal Technology (Beijing, China). Ace2 KO mice have been previously described (Niu et al., 2008).
The obese diabetic Leprdb/db mice at 7–8 weeks of age were used. Adenovirus (5 × 108 particle forming units (pfu) in a total volume of 100 μL of 0.9% wt/vol saline) was introduced into the Leprdb/db mice by tail vein injection. The ad-Ace2 Leprdb/db mice were used at the 6th day post-virus injection. The Leprdb/db mice were treated with Ang-(1-7) by subcutaneous infusion of Ang-(1-7) (100 ng/kg/min) or saline using osmotic mini-pumps (Alzet-Durect, Cupertino, CA, USA Model #1004) for 4 weeks.
Six-week-old male C57BL/6 J mice were used to develop obesity by high-fat (HFD) diet (60 kcal% fat) (Research Diets, New Brunswick, NJ, USA) for 8 weeks, and the mice treated with Ang-(1-7) by osmotic mini-pumps at the 5th weeks post-HFD. Eight- to 10 weeks old male Ace2 KO mice and WT controls, Mas1 KO and WT controls were fed HFD diet for 8 weeks before experimental analysis. The mice were housed in a room at controlled temperature (23°C ± 1°C) with a 12-hr light-dark cycle. All animals were handled in accordance with the protocol approved by the Ethics Committee of Animal Research at Beijing Tongren Hospital, Capital Medical University, Beijing, China.
BAT transplantation
Request a detailed protocolAccording to the methods described previously (Liu et al., 2013; Yuan et al., 2016), BAT was removed from the interscapular region of 8 week old Mas1 KO mice or C57BL/6 mice donor mouse and implanted into the interscapular region of recipient mice. BAT of C57B/L6 recipient mice was removed from the interscapular region. After cervical dislocation of donor mice, the BAT or eWAT (also from the epididymal fat pad of 8-week-old C57BL/6 mice) was removed and peripheral white fat was excluded, and then the remaining BAT (0.2 g) or eWAT (0.2 g) was washed with sterile PBS and transplanted into the interscapular region of recipients as quickly as possible. Recipient mice were anesthetized by ip injection with 400 mg/kg body weight avertin, and then BAT or eWAT was transplanted underneath the skin. The recipient mice were then fed an HFD, which began immediately after the transplantation and continued for 10 weeks.
Adipocyte oxygen consumption rate (OCR) measurement
Request a detailed protocolPrimary brown adipose cells were isolated and cultured for 3 days before plated in XF cell culture microplates (Seahorse Bioscience). Cells (10,000 cells) were seeded in each well and each sample has eight replicates. After 6 days of differentiation, cultured adipocytes were washed twice and pre-incubated in XF medium for 2 hr at room temperature. The oxygen consumption rate was measured by the XF extracellular flux analyzer (Seahorse Biosciences). The results were normalized to protein content in each well. The process was cycled three times for baseline and drug injection measurement. Each cycle consisted of 3 min of mix, 2 min of delay, and 3 min of measurement time. The concentrations of the injection compounds used were Oligomycin (1 μM), FCCP (1 μM), and Rotenone/antimycin A (0.5 μM).
Glucose tolerance test (GTT)
Request a detailed protocolMice were fasted for 16 hours (17:00–9:00) with free access to drinking water. Glucose (1.0 g/kg for the Leprdb/db mice and 2.0 g/kg for the HFD mice) was administered intraperitoneally (i.p.), and blood glucose levels were measured immediately 0, 15, 30, 60, and 120 min after glucose injection by using an Accu-Chek glucose monitor (Roche Diagnostics Corp).
Insulin tolerance test (ITT)
Request a detailed protocolITT was performed by injecting intraperitoneally 0.75 IU/kg of insulin at mice fasted for 1 hr and measured blood glucose levels at 0, 15, 30, 60, 90, and 120 min post injection by using an Accu-Chek glucose monitor (Roche Diagnostics Corp).
RNA extraction and quantitative real-time RT-PCR
Request a detailed protocolTotal RNA was isolated using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. A total of 500 ng of RNA was used as the template for the first-strand cDNA synthesis using ReverTra Ace qPCR RT Kit (TOYOBO, Osaka, Japan) in accordance with the manufacturer’s protocol. The transcripts were quantified using Light Cycler 480 Real-Time PCR system (Roche, Basel, Switzerland). Primers were designed using Primer Quest (Integrated DNA Technologies, Inc).
Positron emission tomography–computed tomography (PET-CT)
Request a detailed protocolSiemens Inveon Dedicated PET (dPET) System and Inveon Multimodality (MM) System (CT/SPECT) (Siemens Preclinical Solutions) was used to detect PET-CT imaging at Chinese Academy of Medical Sciences. According to the previously studies (Liu et al., 2013; Yuan et al., 2016), mice were allowed to fast overnight and were lightly anesthetized with isoflurane, and then followed by a tail vein injection of 18F-FDG (500 mCi). Sixty minutes after the injection of the radiotracer, the mice were subjected to PET/CT analysis. A 10 min CT X-ray for attenuation correction was scanned before PET-CT scan. Static PET-CT scans were acquired for 10 min, and images were reconstructed by an OSEM3D algorithm followed by Maximization/Maximum a Posteriori (MAP) or Fast MAP provided by Inveon Acquisition Workplace (IAW) software. The 3D regions of interest (ROIs) were drawn over the guided CT images, and the tracer uptake was measured using Inveon Research Workplace (IRW) (Siemens) software. Individual quantification of the 18F-FDG uptake in each of the ROI was calculated. The data for the accumulation of 18F-FDG on micro-PET images were expressed as the standard uptake values (SUVs), which were determined by dividing the relevant ROI concentration by the ratio of the injected activity to the bodyweight.
Western blot analysis
Request a detailed protocolTissues were dissolved in RIPA buffer (150 mM sodium chloride, 1.0% Triton X-100, 0.5% sodium deoxycholate, 0.1% SDS, 50 mM Tris, protease and phosphatase inhibitor mixture (Roche Diagnostics)). Protein concentrations were determined using a BCA assay kit (Pierce Diagnostics). Protein was separated by 10% (wt/vol) SDS/PAGE, transferred to a PVDF membrane (Millipore), blocked in 5% (wt/vol) skim milk in TBST (0.02 M Trisbase, 0.14 M Vehicle, 0.1% Tween 20, pH 7.4), and incubated with primary antibodies overnight at 4 °C and then incubated with secondary antibodies conjugated with HRP. The following primary antibodies were used: anti-UCP1 (ab10983, Abcam), anti-PGC1ɑ (ab54481, Abcam), anti-OXPHOS (ab110413, Abcam), anti-Mas1 (AAR-013, Alomone labs), anti-Akt (#9272, cell signaling technology), anti-p-Akt308 (#13038, cell signaling technology), anti-FoxO1 (#2880, cell signaling technology), anti-p-FoxO1 (#84192, cell signaling technology), anti-PKA (#4782, cell signaling technology), anti-p-PKA (#9621, cell signaling technology), anti-ACE2 (#92485, cell signaling technology), and actin (#4970, Cell Signaling Technology). Signals were detected with Super Signal West Pico Chemiluminescent Substrate (Pierce).
Histology and immunofluorescence analysis
Request a detailed protocolTissues fixed in 4% paraformaldehyde were sectioned after being paraffin embedded. Multiple sections were prepared and stained with hematoxylin and eosin for general morphological observations. Cells grown on poly-L-lysine (Sigma)-pretreated coverslips were fixed with 4% paraformaldehyde. Immunofluorescence staining was performed according to the standard protocol using the following antibodies and dilutions: UCP1 (1:100 dilution; Santa Cruz Biotechnologies), MitoTracker Red (1:1,000 dilution; Invitrogen). Incubations were performed overnight in a humidified chamber at 4 °C. 40, 6-diamidino-2-phenylindole staining was used to mark the cell nuclei. The images were acquired by microscope (DS-RI1; Nikon).
Metabolic rate and physical activity
Request a detailed protocolOxygen consumption and physical activity were determined with a TSE LabMaster, as previously described (Chi and Wang, 2011). Mice were acclimated to the system for 24 hr, and then VO2 and VCO2 were measured during the next 24 hr. Voluntary activity of each mouse was measured with an optical beam technique (Opto-M3, Columbus Instruments, Columbus, OH, USA) over 24 hr and expressed as 24 hr average activity. Energy expenditure and respiratory exchange ratio were then calculated (Liu et al., 2013).
RNA-Seq analysis
Request a detailed protocolTotal RNA was extracted from Ace2 KO or WT primary brown adipocytes by Trizol reagent (Invitrogen), respectively. Extracted RNA samples were sent to Novel Bioinformatics company (Shanghai, China) for RNA-seq. RNA with RIN >8.0 is right for cDNA library construction. The cDNA libraries were processed for the proton sequencing according to the commercially available protocols. Data were submitted to the GEO archive. Fisher’s exact test was calculated to select the significant pathway, and the threshold of significance was defined by p-value and false discovery rate (FDR) (Dupuy et al., 2007).
Infrared thermography and core temperature
Request a detailed protocolMice were exposed to a cold chamber (4 °C) with one mouse per cage for up to 6 hr, with free access to food and water. An infrared digital thermographic camera was used to taken images (E60: Compact Infrared Thermal Imaging Camera; FLIR). The images were analyzed by FLIR Quick Report software (FLIR ResearchIR Max 3.4; FLIR). A rectal probe connected to a digital thermometer was used to measure core body temperature (Yellow Spring Instruments).
Statistical analysis
Request a detailed protocolAll of the data are presented as the mean ± SEM. The data were analyzed by Student’s t-test or one-way ANOVA (with Bonferroni post-hoc tests to compare replicate means) when appropriate. Statistical comparisons were performed using Prism5 (GraphPad Software, San Diego, CA). The CLAMS data were performed using ANCOVA on webtool (https://calrapp.org/) (Mina et al., 2018). p Values less than 0.05 were considered statistically significant. Representative results from at least three independent experiments are shown unless otherwise stated.
Data availability
All data generated or analysed during this study are included in the manuscript and supporting file.
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Article and author information
Author details
Funding
National Natural Science Foundation of China (81930019)
- Jin-Kui Yang
National Natural Science Foundation of China (81561128015)
- Jin-Kui Yang
National Natural Science Foundation of China (81670774)
- Xi Cao
National Natural Science Foundation of China (82070850)
- Xi Cao
Beijing Natural Science Foundation (7162047)
- Xi Cao
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Acknowledgements
This work was supported by grants from National Key R&D Program of China (2017YFC0909600) and National Natural Science Foundation of China (81561128015, 81471014) to Jinkui Yang, National Natural Science Foundation of China (81670774, 82070850) and Beijing Natural Science Foundation (7162047) to Xi Cao.
Ethics
All animal protocols used in this study were reviewed and approved by the Ethics Committee of Animal Research at Beijing Tongren Hospital, Capital Medical University (#2017-0107).
Copyright
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
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