The maintenance of a constant ATP level (‘set-point’) is a vital homeostatic function shared by eukaryotic cells. In particular, mammalian myocardium exquisitely safeguards its ATP set-point despite 10-fold fluctuations in cardiac workload. However, the exact mechanisms underlying this regulation of ATP homeostasis remain elusive. Here we show mitochondrial flashes (mitoflashes), recently discovered dynamic activity of mitochondria, play an essential role for the auto-regulation of ATP set-point in the heart. Specifically, mitoflashes negatively regulate ATP production in isolated respiring mitochondria and, their activity waxes and wanes to counteract the ATP supply-demand imbalance caused by superfluous substrate and altered workload in cardiomyocytes. Moreover, manipulating mitoflash activity is sufficient to inversely shift the otherwise stable ATP set-point. Mechanistically, the Bcl-xL-regulated proton leakage through F1Fo-ATP synthase appears to mediate the coupling between mitoflash production and ATP set-point regulation. These findings indicate mitoflashes appear to constitute a digital auto-regulator for ATP homeostasis in the heart.https://doi.org/10.7554/eLife.23908.001
A small molecule called ATP is often referred to as the primary “energy currency” of living cells. It is required to power tasks as diverse as the general housekeeping processes that keep all cells alive to the programmed cell death response that dismantles any cells that are no longer needed. It is also crucial that cells maintain a constant level of ATP at all times, even when the supply of and demand for ATP fluctuate. This control is particularly important in the mammalian heart where the rates of ATP production and consumption change ten-fold during intense exercise. Despite intensive research over the past decades, it was still not known how cells keep ATP levels constant.
In many cell types, including heart muscle cells, ATP is mainly produced inside compartments called mitochondria. Each heart muscle cell contains between 5,000 and 8,000 mitochondria. Recent experiments have shown that ATP production in mitochondria is interrupted by ten-second bursts called “mitochondrial flashes” (or mitoflashes for short), during which the mitochondria release chemicals called reactive oxygen species. The mitoflashes are tightly linked with energy usage, and Wang, Zhang, Wu et al. have now explored if and how mitoflashes regulate ATP levels in the heart.
Experiments on isolated mitochondria from mouse heart muscle cells showed that mitoflashes inhibit the production of ATP. When the intact heart muscle cells were given excess of the building blocks needed to produce ATP – mitoflashes occurred more often. Conversely, when the cells were forced to contract more quickly, which increased demand for ATP, the mitoflashes occurred less often. Importantly, the level of ATP inside the cells actually remained constant in the experiments. Furthermore, inhibiting mitoflashes with antioxidants increased the ATP concentration in heart muscle cells. Lastly, Wang et al. demonstrated that mitoflashes could be triggered under certain conditions.
Overall, these experiments uncovered a way in which highly active cells can maintain a constant level of ATP. Future studies are needed to understand exactly how mitoflashes are initiated and how they in turn inhibit ATP production. A better understanding of these processes might uncover molecules that could be targeted by drugs to the control of the rate of ATP production to treat heart failure.https://doi.org/10.7554/eLife.23908.002
ATP is the most important energy currency and mitochondria constitute the largest cellular powerhouse, supplying ATP at a rate of ~6 kg/day in the human heart (Neubauer, 2007). More than an energy currency, ATP also plays diverse roles in physiological processes including signal transduction, ion channel regulation, cytoskeleton remodelling, and gene transcription (Rolfe and Brown, 1997). The regulation of intracellular ATP concentration is therefore a vital homeostatic function shared by all tissues and eukaryotic cells. An exemplary case is found in mammalian myocardium - the rate of energy consumption and supply (i.e., ATP flux) augments by 5–10 folds in situations of fight-or-flight or exercise, but the ATP concentration (i.e., ATP set-point) remains remarkably constant (Balaban et al., 1986; Neely et al., 1973; Matthews et al., 1981; Allue et al., 1996). The mechanism underlying such exquisite ATP homeostatic regulation has been extensively pursued over the last several decades. ADP, Pi and Ca2+ have been suggested to be regulators of ATP homeostasis, but challenges exist because of the relative constancy of ADP and Pi (Katz et al., 1989; Yaniv et al., 2010; Balaban, 2012) and the extremely low activity of the mitochondrial Ca2+ uniporter (MCU) in cardiac myocytes (Fieni et al., 2012; Williams et al., 2013). Moreover, recent findings in MCU knockout mice suggest that MCU is dispensable for energy metabolism except under extreme physiological stress (Pan et al., 2013). Myocardial overexpression of the dominant negative MCU increases, rather than decreases, mitochondrial oxygen consumption due in part to secondary effect on cytosol Ca2+ homeostasis (Rasmussen et al., 2015). To date, deciphering the exact mechanism underlying ATP set-point regulation in the heart remains an unmet challenge.
Mitochondrial flash (mitoflash) represents a recently discovered dynamic activity of the mitochondria (Wang et al., 2008) and has been ubiquitously detected in all eukaryotic species examined, from C. elegans to zebrafish and to rodents and humans (Wang et al., 2008; Hou et al., 2014; Wang et al., 2016a; Shen et al., 2014; Zhang et al., 2015). Individual mitoflash consists of multiple signal components including bursting superoxide production, transient matrix alkalization, oxidative redox shift, transient depletion of the electron donors NADH and FADH2, and mitochondrial membrane potential depolarization (Wang et al., 2008, 2016b). The generation of mitoflashes in intact cells requires the integrity of the electron transfer chain (ETC) (Wang et al., 2008); and mitoflash frequency is highly regulated over a wide dynamic range by factors including metabolic state, thus the mitoflash activity is considered a biomarker for mitochondrial energy metabolism under certain conditions (Wei et al., 2011; Pouvreau, 2010; Fang et al., 2011; Gong et al., 2015). Most recently, we have shown that protons produced by photolysis or electroneutral proton ionophores act as a powerful mitoflash trigger (Wang et al., 2016b). This finding is instructive because, in the Mitchell chemiosmotic theory of ATP synthesis (Nicholls and Ferguson, 2002; Mitchell, 1961), proton gradients, vectorial proton movement, and proton motive force (ΔμH) across the inner mitochondrial membrane are quintessential for energy metabolism. Thus, the mitoflash biogenesis may be mechanistically and functionally intertwined with energy metabolism at multiple levels.
Emboldened by these recent advances, we revisited the fundamental question of ATP set-point regulation. Our central hypothesis to be tested is that mitoflashes might provide the long-sought regulatory mechanism for ATP homeostasis in the mammalian heart. In particular, we sought to determine whether mitoflash activity is able to regulate mitochondrial ATP production, how mitoflash responds to altered ATP supply and expenditure, and whether manipulation of mitoflashes can reset the level at which the cellular ATP concentration is maintained stable. In the scenario that mitoflash emerges as the ATP set-point regulator, we also attempted to identify a possible physiological trigger that couples the mitoflash activity with the regulation of ATP homeostasis. Our findings indicate that, by sensing and counteracting the ATP supply-and-demand imbalance, mitoflashes appear to constitute a digital auto-regulator for the maintenance of ATP homeostasis in the heart.
To interrogate a possible role of mitoflashes in the regulation of ATP homeostasis, we first determined whether mitoflashes exert any direct effect on mitochondrial metabolic activity and, in particular, ATP production. To circumvent complicated homeostatic regulation at the cellular level, we opted to use isolated cardiac mitochondria freshly prepared from mt-cpYFP-transgenic mouse hearts (Wang et al., 2008). While the mitochondrial respiration was supported by the presence of succinate, ADP and phosphate, mitoflash activity was visualized with confocal imaging, and the rate of ATP production was measured with the luciferin luminescence method (Jouaville et al., 1999). We found that mitoflash events occurred randomly at a rate of 26 ± 2 events / (1000 µm2·100s) (Figure 1A and B) and individual mitoflashes exhibited an average rise time of 7 s, peak amplitude of 0.5 (ΔF/F0), and duration of 22 s, comparable with those in intact cardiac myocytes (Figure 1—figure supplement 1). Treatments using the mitochondria-targeted antioxidants, SS31 and mitoTEMPO, or the mitochondrial permeability transition pore (mPTP) inhibitor cyclosporin A (CsA) decreased the mitoflash frequency by 44%, 31%, and 47% (Figure 1A and B), whereas the amplitudes and time courses of mitoflashes were largely unchanged (Figure 1—figure supplement 1). Parallel luciferin luminescence measurement showed that, along with the repression of mitoflash activity, the rate of ATP production, assessed as the cumulative ATP formation over a 5 min time window, was enhanced by 25%, 24%, and 22%, respectively (Figure 1C). This result suggests that mitoflashes negatively regulate ATP production at the organelle level. In other words, mitoflash activity may also be directly involved in the regulation of energy metabolism, in addition to serving a biomarker of respiratory activity (Gong et al., 2015).
To investigate whether or not mitoflash activity responds to altered energy metabolism, we first tipped the ATP supply-and-demand balance by altering mitochondrial substrate supply in intact cardiac myocytes. As shown in Figure 2A, all metabolites examined, including glucose, free fatty acid and pyruvate, dose-dependently increased the mitoflash frequency, consistent with previous reports (Fang et al., 2011; Pouvreau, 2010; Wei et al., 2011; Gong et al., 2015). Strikingly, 10 mM pyruvate, the immediate metabolite that enters mitochondria and feeds the tricarboxylic cycle, elicited the most vigorous mitoflash activity, increasing the mitoflash frequency by 12 folds comparing to 5.6 mM glucose (Figure 2A). This stimulatory effect on mitoflash activity was fully reversed upon pyruvate washout, and was largely prevented by α-cyano-4-hydroxycinnamic acid, an inhibitor of the mitochondrial pyruvate transporter (Figure 2A). Likewise, a large and robust mitoflash response was obtained in beating hearts under Langendorff perfusion: switching from 5.6 mM glucose to 10 mM pyruvate augmented the mitoflash frequency from 1.2 ± 0.3 to 11.5 ± 2.8 mitoflashes / (1000 µm2·100s) (Figure 2B).
Parallel measurements revealed that the intracellular ATP content (measured with the luciferin luminescence method) and the ATP/ADP ratio (measured with the indicator PercevalHR [Tantama et al., 2013]) exhibited an initial overshoot upon the glucose-to-pyruvate switch and returned to its baseline in about 100 s (Figure 2C), indicating a transient escape of homeostatic control of the ATP level. Interestingly, the time-course response of mitoflashes showed that the significant rise of mitoflash activity occurred concomitantly with a decline in the ATP transient (Figure 2C). Along with the high activity of mitoflashes at the steady state, the rate of oxygen consumption and the cellular levels of NADH and FADH2 were all increased despite the constancy of ATP (Figure 2D–2F), indicative of decreased efficiency of ATP synthesis and substantiating the conclusion that mitoflashes negatively regulate ATP production. Thus, the higher mitoflash activity in response to superfluous substrate supply tends to dampen ATP production and restore the ATP concentration to its set-point.
In the second set of experiments, we aimed to investigate the response of mitoflashes to ATP supply-and-demand imbalance caused by altering energy expenditure. In cardiac myocytes, a single heartbeat consumes ~2% of the cellular ATP (Jacobus, 1985). The higher the heart rate, the greater is the rate of ATP expenditure and replenishment. We therefore assessed the mitoflash response to electrical pacing at various frequencies. To minimize interference from cell shortening, image acquisition in contracting cells was synchronized with the electrical pacing (See Materials and methods). The mitoflash activity in pyruvate-treated cells declined precipitously at the onset of electrical pacing, alongside the onset of intracellular Ca2+ transients and cell shortenings; it was readily restored at the offset of pacing, with the cessation of Ca2+ and contractile responses (Figure 3A and Figure 3—figure supplement 3). Quantitatively, mitoflash frequency was diminished by 45% at 1 Hz, 69% at 2 Hz, and 80% at 5 Hz pacing (Figure 3B). Similar results were found in cardiomyocytes exposed to physiological 5.6 mM glucose in Tyrode’s solution, i.e., increasing the workload inhibited rather than stimulated mitoflash activity (Figure 3C). Remarkably, the cellular ATP content and ATP/ADP ratio were held constant regardless of pacing at different frequencies (Figure 3D), substantiating the tightness of the ATP set-point regulation.
Because the oxidative phosphorylation (OXPHOS) activity is expected to be elevated upon increasing workloads, together with the results in Figure 2, it is clear that the mitoflash frequency is not a unique function of mitochondrial respiration. This finding reinforces the notion that mitoflash plays an active role on its own. To this end, we noticed that the rapid and reversible mitigation of mitoflash activity in response to pacing and the inverse relation between mitoflash activity and pacing frequency fit naturally the cell logic that the mitoflash acts as a rapid and sensitive responder to altered ATP demand. For instance, when the ATP demand is augmented at the onset of pacing, the mitoflash activity is downregulated to alleviate its inhibition on ATP production (Figure 1), leading to increased ATP supply. Similar reasoning is applicable to explain the equally fast mitoflash changes on cessation of electrical pacing. Taken together, we propose a unifying interpretation - mitoflash acts as a reporter of ATP supply-and-demand imbalance and an ATP homeostasis regulator through negative regulation of ATP production. That mitoflash can serve as the biomarker of mitochondrial respiration is merely a special case when the substrate supply is changed and at the same time the ATP demand is held constant.
Paradoxically, pacing-induced suppression of mitoflashes occurred concurrently with the onset of large cyclic intracellular Ca2+ transients, opposite to the prediction of Ca2+-dependent activation of mitoflashes in different cell types including cardiac myocytes (Jian et al., 2014; Gong et al., 2014). This discrepancy is only apparent, because cardiac mitochondria are relatively inert in terms of Ca2+ uptake (Fieni et al., 2012; Williams et al., 2013; Chen et al., 2011a) and a prolonged pacing protocol elicited only a moderate mitoflash-stimulatory effect as an after-effect (Gong et al., 2014). Thus, the bioenergetics-dependent mechanism might be more powerful than the Ca2+-dependent mechanism, thus dominating the mitoflash response in the present experimental conditions.
Next, we extended our studies to other situations of altered ATP demand. Even in quiescence, it takes a significant portion of energy expenditure for a cardiac myocyte to maintain physiological Ca2+ gradients across different compartments. In this regard, we demonstrated that β-adrenergic stimulation with isoproterenol (ISO, 1 μM), to enhance Ca2+ cycling and thus to increase ATP demand, inhibited mitoflash frequency by 70% in pyruvate-treated cells (Figure 3E). In contrast, brief removal of extracellular Ca2+ (5 mM EGTA in nominal 0 Ca2+ solution) increased mitoflash activity by 48% (Figure 3E). These results provide additional lines of evidence that mitoflash regulation is dominated by bioenergetics - rather than Ca2+-dependent mechanism in the present experimental settings. Notably, the ATP content and ATP/ADP ratio were kept constant under either ISO stimulation or Ca2+ manipulation (Figure 3F and G). Taken together, both sets of experiments unveil a unifying interpretation of the mitoflash responses: mitoflash activity waxes and wanes in accordance with the ATP supply-and-demand imbalance, with higher activity occurring in response to over-exuberant ATP supply or diminished ATP demand, and vice versa.
The above results indicate that mitoflashes responding to altered energy supply and demand safeguard the ATP-set-point. The question arises whether tuning mitoflash activity can shift the ATP set-point when both energy expenditure and substrate supply are held unchanged. To answer this question, we inhibited mitoflashes with mitochondria-targeted antioxidants SS31 or mitoTEMPO, or overexpression of SOD2 in intact cardiac myocytes. As shown in Figure 4A and B, all these manipulations decreased mitoflash frequency and increased the ATP content even in intact cardiac myocytes. Quantitatively, the ATP set-point was elevated by ~60% while the mitoflash activity was mitigated by ~40% (Figure 4A and B). Linear regression revealed a strong inverse correlation between the mitoflash activity and the cellular ATP content (r = −0.96, p=0.009) (Figure 4B). A similar trend was seen in cells under physiological condition (at 5.6 mM glucose) displaying a lower basal mitoflash incidence (r = −0.79, p=0.11) (Figure 4C and D). Together with the above findings that mitoflashes inhibits ATP production, this result indicates that mitoflash activity is a potent ATP set-point regulator in cardiac myocytes.
The above results indicate that mitoflashes regulate the cellular ATP homeostasis in a digital and frequency-modulatory manner. Then, what is the specific mechanism that senses the ATP supply-and-demand imbalance and regulates mitoflash activity? To date, three mitochondrial signals have been shown to be effective triggers or activators of mitoflashes, i.e., matrix Ca2+, basal ROS, and protons (at nanodomains of the inner mitochondrial membrane) (Hou et al., 2013; Jian et al., 2014; Wang et al., 2016b). Mitochondrial Ca2+ is unlikely the candidate signal for the bioenergetics-dependent mitoflash activity, because no apparent Ca2+ changes were detected upon pyruvate-stimulated mitoflash activation (Figure 5—figure supplement 1A) and electrical pacing elicited opposite mitoflash and Ca2+ responses. Moreover, inhibiting MCU with Ru360 did not show any significant effect on mitoflash frequency (Figure 5—figure supplement 2). The lack of significant effect of Ru360 on mitoflashes in cardiomyocytes is expected because pyruvate treatment did not induce any changes in cytosolic Ca2+ and thus mitochondrial Ca2+ uptake (Figure 5—figure supplement 1A). However, mitoflash is sensitive to MCU inhibition in situations when it is induced by elevations of mitochondrial Ca2+, e.g., in HeLa cells under hyperosmotic stress or high cytosolic Ca2+ stimulation (in permeabilized cells) (Hou et al., 2013; Jian et al., 2014). Further, electrical pacing did not alter (Figure 5—figure supplement 1C) and pyruvate stimulation caused a slight decrease of mitochondrial ROS (Figure 5—figure supplement 1B), indicating that ROS are unlikely a major player, either. TMRM measurement revealed little effects of these manipulations on ΔΨm, excluding changes in ΔΨm as a possible cause of the mitoflash response (Figure 5—figure supplement 1D). Given that protons act as a potent trigger of mitoflashes (Wang et al., 2016b), we reckoned that ATP synthesis-uncoupled proton entry might be a logic candidate for the trigger of mitoflashes to counteract the ATP supply-and-demand imbalance.
While proton entry at the F1Fo-ATP synthase drives ATP production, there exist multiple routes for ATP synthesis-uncoupled futile proton entry, and varying the proportion of the coupled and uncoupled proton entry would effectively alter the metabolic efficiency. We therefore determined the proton leakage by measuring the ATP-synthesis uncoupled oxygen consumption rate (OCR). Interestingly, we found that the proton leakage associated OCR was augmented by 28% in response to increasing ATP supply, i.e. 10 mM pyruvate stimulation (Figure 5—figure supplement 3). Increasing workloads by ISO treatment attenuated the proton leakage associated OCR by 11% while decreasing energy expenditure by brief removal of extracellular Ca2+ (5 mM EGTA in nominal 0 Ca2+ solution) elevated the proton leakage associated OCR by 14% (Figure 5—figure supplement 3). This result indicates that the ATP-synthesis uncoupled proton leakage varies in accordance with the changes of ATP supply and demand, consistent with its role in sensing the ATP supply-and-demand imbalance and triggering mitoflashes.
In search for the specific uncoupled proton leak for the triggering of mitoflashes, we examined possible involvement of proton leakage through mitochondrial uncoupling proteins (UCPs). Inhibition of UCP2, the dominant isoform of UCPs in heart (Ricquier and Bouillaud, 2000) (Figure 5—figure supplement 4) with either genipin (Zhang et al., 2006) or RNA interference, slightly increased, rather than decreased, the mitoflash incidence (Figure 5A–5C and Figure 5—figure supplement 4). This result excludes UCPs as the source of mitoflash-triggering proton flux. Recently, a Bcl-xL-regulated proton leakage through F1Fo-ATPase has been demonstrated with multiple approaches, including patch-clamping of sub-mitochondrial vesicles, proton flux measurement, and immunochemical demonstration of a Bcl-xL interaction with the β-subunit of ATP synthase in hippocampal neuronal mitochondria (Alavian et al., 2011; Chen et al., 2011b). We therefore turned our attention to this F1Fo-ATPase-mediated proton leakage with its hallmark sensitivity to Bcl-xL regulation. Indeed, we found that Bcl-xL overexpression, to inhibit the uncoupled proton flux, markedly decreased mitoflash incidence, whereas knockdown of Bcl-xL with siRNAs (Figure 5—figure supplement 5), increased mitoflashes at both 5.6 mM glucose and 10 mM pyruvate (Figure 5D and E). Likewise, treatment with ABT-737, a mimetic of BH3-only proteins that inhibits Bcl-xL (Oltersdorf et al., 2005), also elevated mitoflash production (Figure 5D). Furthermore, the mitoflash responses were accompanied by a 19% upward shift of the ATP set-point with Bcl-xL overexpression, and an 11% downward shift with ABT-737 treatment (Figure 5F and G). These lines of evidence support the notion that proton leakage through ATP synthase is an important physiological trigger of mitoflashes, coupling the mitoflash biogenesis with auto-regulation of ATP homeostasis in cardiac myocytes.
It has been established for decades that myocardial ATP level remains constant in the face of large fluctuations in the rate of ATP consumption and production. Indeed, the present results show that the ATP content and ATP/ADP ratio are held constant regardless of electrical pacing, altered substrate supply, receptor stimulation, and Ca2+ manipulations in isolated single cardiac myocytes, attesting to the exquisiteness of the ATP set-point regulation. Ironically, as ADP, Pi and Ca2+ have been dismissed as the major players, the exact mechanism underlying ATP set-point regulation remains an unsolved enigma. From the design principle of control systems, at least three criteria should be met for any candidate mechanism to be qualified as an ATP set-point regulator. First, it should have an impact on mitochondrial ATP production through the OXPHOS process. Second, it should respond to cellular ATP supply-demand imbalance. More specifically, its direction of response should counteract the imbalance and its dynamic range as well as kinetics of response should be robust and fast enough to cope with 10-fold fluctuations of ATP supply and demand on a beat-to-beat basis. Third, actively tuning this regulatory mechanism should be able to reset the ATP level in situations when the ATP supply and demand are held unaltered. Additional mechanism is also required to sense the state of ATP supply-demand imbalance and to couple the regulator’s response with the OXPHOS process. In this scenario, the major finding of the present study is that the recently-discovered, digital mitoflash activity meets all these criteria at once.
First, the current study provides direct evidence that mitoflashes negatively regulate ATP production in isolated cardiac mitochondria. Inhibiting mitoflash activity can increase the rate of ATP production by 25%. Multiple mechanisms could contribute to the mitoflash-mediated inhibition of ATP production. First of all, multifaceted energy-consuming processes occur in a mitoflash, including diversion of electrons from energy metabolism to bursting superoxide production, dissipation of ΔΨm, and loss of membrane permeability due to flickering mPTP opening (Wang et al., 2008, 2016b). Albeit the ETC activity is accelerated as indicated by transient matrix alkalization and depletion of the electron-donor pools of NADH and FADH2, ΔμH for ATP synthesis is dissipated because of loss of ΔΨm. All these events indicate that mitochondria undergoing a mitoflash are at a state of futile respiration. That is, intermittent mitoflashes of the ATP-generating organelles are analogous to discharges of the safety-valve of a working steam engine. Second, as ΔμH dissipates, the Complex V could operate in the reverse mode, switching on its ATPase activity and consuming ATP in the flashing mitochondria. Third, mitoflashes may activate some yet-unknown downstream pathways to impose prolonged inhibition of OXPHOS activity. Regardless of specific mechanism of action, the finding that mitoflashes negatively regulate ATP production sheds new light on possible bioenergetics role of this digital activity built-in in the powerhouse of the cell.
Second, based on results from numerous maneuvers purported to perturb the ATP supply-and-demand balance, a unifying pattern emerges in which mitoflashes counteract the imbalance between ATP supply and expenditure, whereby safeguarding the ATP set-point. Specifically, the mitoflash frequency increases with either superfluous substrate supply or diminished energy demand (e.g., offset of electrical pacing, removal of extracellular Ca2+); conversely, it mitigates upon substrate washout or with enhanced workload and energy expenditure (e.g., onset of electrical pacing, β-adrenergic stimulation). Remarkably, the dynamic range of mitoflash frequency spans over an order of magnitude and its kinetics are fast enough to cope with sudden changes occurring in the pacing protocol, allowing for only a transient escape of ATP from its tightly controlled constant level. Thus, compared to the interpretation of mitoflashes as a biomarker of mitochondrial respiration (Gong et al., 2015), which holds true in certain conditions (e.g., varying substrate supply without altering the ATP demand), we re-interpret mitoflashes as a reporter of ATP supply-and-demand imbalance and an ATP set-point regulator through its ability to regulate ATP production.
Third, not only that the mitoflash stabilizes the ATP level in fluctuations of energy expenditure and substrate supply, but also it participates in determining the specific level at which cellular ATP is held stable. When the mitoflash activity is manipulated independently of changes in ATP supply and demand, e.g., by ROS scavenging, SOD2 overexpression, and Bcl-xL manipulation, it can tune the ATP set-point upwardly or downwardly: the higher the mitoflash activity is, the lower the ATP set-point becomes. The negative correlation between mitoflash activity and ATP level attained is in remarkable contrast to the constancy of ATP level in situations of electrical pacing, receptor stimulation and calcium manipulation, and testifies the robustness of this mitoflash-mediated ATP set-point regulation.
It is of interest to note that mitoflash regulation of the ATP set-point bears prominent features of a digital, distributed control system. Individual mitoflashes occur only intermittently, and are confined to single mitochondria. They are digital and operate in the frequency-modulatory mode, i.e, the average amplitude and duration of mitoflashes are relatively constant in different conditions. At the single-mitochondrion level, a mitoflash is a dramatic event blanketing the entire organelle and interrupting the ATP synthesis. In a cardiac myocyte typically containing 5,000–8,000 mitochondria, only a tiny portion of mitochondria undergo the flashing activity at any moment; No central control mechanism is identifiable in this control system, because stochastic mitoflash events are evenly distributed among the population of mitochondria, with their frequency rapidly and tightly regulated in accordance with the ATP supply-and-demand imbalance. Keeping in mind that ATP diffuses freely in the cytosol, such local, stochastic ATP-negating events afford a novel mechanism to finely regulate ATP homeostasis at the cellular level. Taken together, we conclude that mitoflashes act as the long-sought ATP set-point regulator in the mammalian heart.
In search for possible mechanism that couples metabolism and mitoflashes in the context of ATP set-point regulation, we demonstrate that the proton leakage through F1Fo-ATP synthase regulated by Bcl-xL (Chen et al., 2011b; Alavian et al., 2011) provides a physiological proton trigger of mitoflashes for the regulation of metabolic efficiency. Our recent studies have shown that protons at the nanodomains of inner mitochondrial membrane trigger mitoflashes (Wang et al., 2016b), suggesting a possible link between mitoflash biogenesis and the OXPHOS process at the deepest mechanistic level. In the present study, we first show that the ATP synthesis- uncoupled proton leakage varies in accordance with alterations in ATP supply or expenditure, increasing when the supply is superfluous and decreasing when the ATP demand is high. More importantly, we then provide direct evidence that bidirectional manipulations of Bcl-xL-sensitive proton leakage, but not those of UCP2, cause robust, bidirectional changes in the mitoflash frequency and ATP content.
By analogy of local Ca2+ signalling (Cheng and Lederer, 2008), we have envisaged a ‘local control model’ for proton triggering of mitoflashes (Wang et al., 2016b) in order to explain the finding that protons from different sources differ in terms of mitoflash triggering efficiency. Recent numerical analysis has revealed that free protons are short-lived (lifetime ~1.4 ns) and diffuse only over a nanometre scale (~2.1 nm) in the matrix environment (Wang et al., 2016b). Furthermore, free protons are extremely scarce in an alkaline mitochondrial matrix (~0.4 protons in a mitochondrion of 2 μm length and 200 nm diameter at pH 8.0), and matrix pH buffering capacity is estimated to be about 5 mM per pH unit at pH 8.0 (i.e., 1:500,000 for free: bound proton ratio) (Poburko et al., 2011). Thus, we envision that only protons in the nanoscopic vicinity of the putative trigger sites can effectively serve their role as the mitoflash trigger. Consistent with this model, super-resolution microscopy has shown, in the mitochondria from neurons, nanoscale protein partition of UCP4 and F1Fo-ATP synthase, residing in the inner boundary membrane and the cristae membrane, respectively (Klotzsch et al., 2015). Several groups have independently proposed that F1Fo-ATP synthase is of the same molecular identity as that of mPTP (Giorgio et al., 2013; Alavian et al., 2014; Bonora et al., 2013; Bernardi et al., 2015), whose flickering openings signify the ignition of mitoflashes (Wang et al., 2008; Hou et al., 2014). If this picture turns out to be true, both proton leakage and mitoflash triggering would occur within the same macrocomplex protein machinery, thus conferring high selectivity among different proton sources.
In summary, we have presented a set of novel and cohesive findings on mitoflashes as a digital auto-regulator of ATP homeostasis in the heart. First, mitoflashes respond rapidly and robustly to ATP supply-and-demand imbalance, increasing with a superfluous supply and mitigating with a greater demand. Because mitoflashes negatively regulate mitochondrial ATP production, such bioenergetics-dependent mitoflash activity acts as an auto-regulator of the ATP homeostasis (mode I, Figure 6), akin to the safety-valve of a steam engine. Second, tuning the mitoflash activity is able to shift the level at which ATP is held constant (mode II, Figure 6), revealing that mitoflash activity is an important, heretofore unappreciated determinant of the ATP set-point. Third, we demonstrate that the Bcl-xL-sensitive proton leakage through F1Fo-ATP synthase constitutes a physiological proton trigger of mitoflashes (Figure 6). These findings not only mark mitoflashes as the putative auto-regulator for cellular ATP homeostasis, but also uncover compelling cell logic for the biogenesis of mitoflashes in the heart.
Luciferin, carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone (FCCP), pyruvate, palmitate, α-cyano-4-hydroxycinnamic acid (α-CCA), isoproterenol (ISO), blebbistatin, cyclosporin A (CsA), antimycin A, and genipin were from Sigma. Ethylene glycol tetraacetic acid (EGTA) was from Amresco. ABT-737 (ABT) was from Selleck Chemicals (Houston, Texas). Rotenone was from Calbiochem. MitoTEMPO was from Enzo Life Sciences. Mg2+-Green AM, Rhod-4 AM, BCECF AM, and mitoSOX were from Invitrogen (Eugene, Oregon). The tetrapeptide SS31 (D-arg-dmt-lys-phe-NH2) was synthesized as described (Zhao et al., 2004).
All procedures were carried out according to the rules of the American Association for the Accreditation of Laboratory Animal Care International and approved by the Animal Care Committee of Peking University accredited by AAALAC International (IMM-ChengHP-1). This investigation conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85–23, revised 1996).
Single ventricular myocytes were enzymatically isolated from the hearts of adult male Sprague–Dawley rats (200–250 g) or adult C57BL-6 mice (25–35 g), as described previously (Cheng et al., 1993; Shang et al., 2016). Freshly-isolated cardiac myocytes were plated on culture dishes coated with laminin (Sigma) for 1 hr and then the attached cells were cultured in M199 medium (Invitrogen, Carksbad, California) along with (in mM) 5 creatine, 2 L-carnitine, 5 taurine, and 25 HEPES (all from Sigma). Cells were then infected with adenovirus carrying mt-cpYFP, firefly luciferase, Bcl-xL, or the SOD2 gene at an m.o.i. of 20 and experiments were performed after 60–72 hr in culture.
Ventricular myocytes were isolated from 1-day-old Sprague-Dawley rats, as described previously (Shen et al., 2007). Myocytes were plated at 5 × 105 cells/cm2 in DMEM (Invitrogen) supplemented with 10% FBS (Hyclone) in the presence of 0.1 mM 5-bromo-2-deoxyuridine (Sigma). Adenovirus infection or siRNA transfection was implemented after 24 hr quiescence in serum-free DMEM following 48–72 hr culture in DMEM containing 10% FBS. For adenovirus infection, cells were infected with adenovirus carrying mt-cpYFP, mt-GCaMP5 or the Bcl-xL gene at an m.o.i. of 20. For siRNA transfection, 100 nM siRNA was transiently transfected using Lipofectamine RNAiMax (Invitrogen) according to the manufacturer’s instructions. The knockdown efficiency was assessed by western-blot.
The mitochondria were isolated from mouse hearts as previously reported (Zhao et al., 2012). Briefly, mouse hearts were washed with ice-cold isolation buffer (210 mM mannitol, 70 mM sucrose, 5 mM HEPES (pH 7.4), 1 mM EGTA and 0.5 mg/ml BSA), minced, and homogenized. The homogenate was centrifuged at 4°C for 10 min at 1000 g, and the supernatant was collected and further centrifuged at 4°C for 10 min at 12000 g. The pellet was re-suspended for functional assessment.
An inverted confocal microscope (Zeiss LSM 710) with a 40×, 1.3 NA oil-immersion objective was used for imaging. When acquiring the mt-cpYFP signal, images were captured by exciting alternately at 488 and 405 nm, and collecting the emission at >505 nm. For mitoSOX measurement, the indicator (5 μM) was loaded at 37°C for 20 min followed by washing three times. The mitoSOX fluorescence was reported by exciting at 514 nm and collecting the emission at 559–740 nm.
In typical time-series recordings of mitoflashes, 100 frames of 900 × 256 (for adult cardiac myocytes) or 512 × 512 pixels (for neonatal cardiac myocytes) were collected at 0.10–0.14 μm/pixel in bidirectional scanning mode. The frame rate was 30–60 frames/min, and the axial resolution was set to 1.0 μm. All experiments were performed at room temperature (22–26°C) unless specified otherwise.
For ex vivo imaging of mitoflashes, the heart was excised from mt-cpYFP transgenic mice (10–14 weeks old) (Wang et al., 2008), and the ascending aorta was cannulated with a customized needle. The heart was perfused in the Langendorff configuration under constant perfusion pressure (~90 mmHg) with oxygenated (100% O2) Tyrode’s solution consisting of (in mM) 137 NaCl, 5.4 KCl, 1.2 MgCl2, 1.2 NaH2PO4, 1.8 CaCl2, 5.6 glucose or 10 pyruvate, and 20 HEPES (pH 7.35, adjusted with NaOH) at 37°C. The image acquisition plane was focused ~30 μm deep into the epimyocardium and the motion artefacts due to spontaneous beating of the heart were minimized with 10 μM blebbistatin (Sigma).
For imaging mitoflashes in isolated cardiac mitochondria, the mitochondria were suspended in a solution consisting of (in mM) 100 potassium aspartate, 1.0 MgCl2, 20 KCl, 0.5 EGTA, 10 glutathione, 20 HEPES, 8% dextran (MW 35,000–45,000), 10 KH2PO4, 2.5 succinate, and 0.2 ADP (pH 7.2). Typically, 100 frames of 512 × 512 pixels were collected at the rate of 60 frames/min.
In a subset of experiments, electrical field stimulation (5 ms square-wave pulses at 2× threshold voltage) was applied via a pair of platinum electrodes, and cells were perfused with Tyrode’s solution at a rate of 3 ml/min. Cells displaying healthy contractility were chosen for mitoflash measurement and those near the anode, where electrolysis can produce reactive oxygen species locally (Jackson et al., 1986), were avoided. These cautious measures were necessary because we have recently shown that ROS generated by electrolysis of Tyrode’s solution at the anode can cause significant increase in mitoflash as well as mitochondrial Ca2+ (Zhang et al., 2014). To minimize interference from cell shortening, image acquisition in contracting cells was at 1 s/frame and synchronized with the electrical pacing, such that it was phase-locked with cell contraction. In parallel experiments, cell length and cytosolic Ca2+ transients were monitored continuously by placing the scan line along the long axis of the cell. The cytosolic Ca2+ transients were measured by Rhod-4 with excitation at 543 nm and emission collection at 548–646 nm. Fluorescent images of the line were acquired every 3.78 ms and the time-course of cell shortening was extracted from the line-scan images by an edge-detection algorithm.
Cellular ATP content was measured directly with the firefly luciferase-catalysed chemiluminescence method (Jouaville et al., 1999) and indirectly with the small-molecule indicator Mg2+-Green (Campanella et al., 2008). For chemiluminescence measurement, cultured cardiac myocytes expressing firefly luciferase were bathed in Tyrode’s solution with 1 mM luciferin (Sigma). The luminescence was recorded with an electron-multiplying charge-coupled device camera (Andor iXon DU-897D-C00-#BV, Andor Technology, South Windsor, CT) and analysed by AndoriQ software (version 1.0). To measure the ATP content with Mg2+-Green, cells were loaded with 5 μM Mg2+-Green AM and the fluorescence was recorded with excitation at 488 nm and emission at >560 nm.
The cellular ATP/ADP ratio was measured by expressing PercevalHR (Tantama et al., 2013) in cardiac myocytes. Briefly, the PercevalHR fluorescence was acquired by alternate excitation at 488 nm and 405 nm and emission collection at 506–702 nm. To remove the pH bias of PercevalHR, we adopted the procedure developed previously (Tantama et al., 2013). Specifically, the changes of BCECF fluorescence and PercevalHR fluorescence upon pH alterations were recorded and an empirical linear correlation between the PercevalHR signal and the BCECF signal was established for calibration. The pH bias in the PercevalHR signal was corrected by subtracting the estimated pH component based on the pH calibration of PercevalHR and parallel BCECF measurement.
For measuring ATP production in isolated cardiac mitochondria, the isolated mitochondria were suspended in respiration solution containing (in mM) 220 mannitol, 70 sucrose, 5 KH2PO4, 2.5 MgCl2, 0.5 EDTA, 2.5 succinate, 0.2 ADP, 2 HEPES (pH7.4), and 0.1% BSA. The ATP content was measured with the luciferase assay (Promega, Madison, Wisconsin).
Oxygen consumption rate in intact adult cardiac myocytes was measured with a Clark-type oxygen electrode (Strathkelvin 782 2-Channel Oxygen System version 1.0; Strathkelvin Instruments, Motherwell, UK). Briefly, 1 × 105 cells were suspended in Tyrode’s solution containing 5.6 mM glucose or 10 mM pyruvate and the oxygen consumption was measured over 10 min with the Strathkelvin System.
To measure ATP synthesis-uncoupled oxygen consumption rate, the mouse cardiac myocytes were cultured in XF24 cell-culture microplates (Seahorse Bioscience). The cells were suspended in different medium: Tyrode’s solution with 5.6 mM glucose, Tyrode’s solution with 10 mM pyruvate, Tyrode’s solution with 10 mM pyruvate and 1 μM ISO, nominal 0 Ca2+ Tyrode’s solution with 10 mM pyruvate and 5 mM EGTA. Bioenergetics analyses were performed in an XF24 Extracellular Flux Analyzer (Seahorse Bioscience) with the injection of oligomycin (1 μM), FCCP (1 μM), and rotenone (1 μM) and antimycin A (1 μM) sequentially. The uncoupled oxygen consumption rate was calculated as the oligomycin-insensitive percentage relative to basal oxygen consumption.
Cell lysates were separated by 4–12% NuePAGE (Invitrogen) and transferred to nitrocellulose membranes (Millipore). Membranes were blocked with 5% non-fat dry milk and incubated with primary antibody overnight at 4°C. Monoclonal anti-UCP2 antibody (Santa Cruz Biotechnology, California), monoclonal anti-Bcl-xL (Sigma), polyclonal anti-SOD2 (Abcam, RRID:AB_300434), and anti-α-tubulin antibody (Sigma, RRID:AB_477593) were used. Blots were visualized using secondary antibodies conjugated with IRDye (LI-COR, Lincoln, Nebraska) and an Odyssey imaging system (LI-COR).
Total RNA was extracted from adult or neonatal cardiac myocytes using Trizol reagent (Invitrogen) and converted to cDNA using M-MLV reverse transcriptase (TaKaRa, Japan) with oligo-dT primers. Quantitative real-time PCR was performed using Trans Start Green qPCR Super Mix (TransGen Biotech, China) with primers designed with the NCBI/Primer-BLAST tool (see the following table for the primer sequences). The Ct values were obtained using CFX Manager Quantification software (BioRad, Hercules, California) and the relative expression of target genes was analysed by comparison with 18S rRNA.
Confocal images were analysed using custom-developed programs written in Interactive Data Language (IDL, ITT). Cell-motion artefacts and background fluorescence changes were corrected by image processing and individual mitoflashes were located with the aid of FlashSniper (Li et al., 2012; LJHIS007, 2017; https://github.com/ljhis007/flashsniper. A copy is archived at https://github.com/elifesciences-publications/flashsniper).
Data are expressed as mean ± SEM. When appropriate, Student’s t-test was applied to determine the statistical significance, and a simple linear regression model was used to investigate the correlation between mitoflash activity and ATP content. The coefficient of determination (R2) was used to evaluate the goodness of fit of the model. Prism linear regression analysis was used for the statistical analysis. p<0.05 was considered statistically significant. The number of samples chosen for each comparison was determined based on past similar experiments.
Perspectives on: sgp symposium on mitochondrial physiology and medicine: metabolic homeostasis of the heartThe Journal of General Physiology 139:407–414.https://doi.org/10.1085/jgp.201210783
Differential mitochondrial calcium responses in different cell types detected with a mitochondrial calcium fluorescent Indicator, mito-GCaMP2Acta Biochimica Et Biophysica Sinica 43:822–830.https://doi.org/10.1093/abbs/gmr075
Bcl-xL regulates mitochondrial energetics by stabilizing the inner membrane potentialThe Journal of Cell Biology 195:263–276.https://doi.org/10.1083/jcb.201108059
Activity of the mitochondrial calcium uniporter varies greatly between tissuesNature Communications 3:1317.https://doi.org/10.1038/ncomms2325
Regulation of metabolism in individual mitochondria during excitation-contraction couplingJournal of Molecular and Cellular Cardiology 76:235–246.https://doi.org/10.1016/j.yjmcc.2014.09.012
Mitochondrial flash as a novel biomarker of mitochondrial respiration in the heartAmerican Journal of Physiology - Heart and Circulatory Physiology 309:H1166–H1177.https://doi.org/10.1152/ajpheart.00462.2015
Synergistic triggering of superoxide flashes by mitochondrial Ca2+ uniport and basal reactive oxygen species elevationJournal of Biological Chemistry 288:4602–4612.https://doi.org/10.1074/jbc.M112.398297
Mitochondrial flashes: new insights into mitochondrial ROS signalling and beyondThe Journal of Physiology 592:3703–3713.https://doi.org/10.1113/jphysiol.2014.275735
Electrolysis-induced myocardial dysfunction: a novel method for the study of free radical mediated tissue injuryJournal of Pharmacological Methods 15:305–320.https://doi.org/10.1016/0160-5402(86)90010-0
Regulation of superoxide flashes by transient and steady mitochondrial calcium elevationsScience China Life Sciences 57:495–501.https://doi.org/10.1007/s11427-014-4628-z
Flashsniper, version c423bdbGithub.
The steady-state rate of ATP synthesis in the perfused rat heart measured by 31P NMR saturation transferBiochemical and Biophysical Research Communications 103:1052–1059.https://doi.org/10.1016/0006-291X(81)90915-3
Dynamic regulation of the mitochondrial proton gradient during cytosolic calcium elevationsJournal of Biological Chemistry 286:11672–11684.https://doi.org/10.1074/jbc.M110.159962
The uncoupling protein homologues: UCP1, UCP2, UCP3, StUCP and AtUCPBiochemical Journal 345:161–179.https://doi.org/10.1042/bj3450161
Cyclophilin D regulates mitochondrial flashes and metabolism in cardiac myocytesJournal of Molecular and Cellular Cardiology 91:63–71.https://doi.org/10.1016/j.yjmcc.2015.10.036
Mitofusin-2 is a Major determinant of oxidative stress-mediated heart muscle cell apoptosisJournal of Biological Chemistry 282:23354–23361.https://doi.org/10.1074/jbc.M702657200
Mitochondrial flash: integrative reactive oxygen species and pH signals in cell and organelle biologyAntioxidants & Redox Signaling 25:534–549.https://doi.org/10.1089/ars.2016.6739
Matching ATP supply and demand in mammalian heart: in vivo, in vitro, and in silico perspectivesAnnals of the New York Academy of Sciences 1188:133–142.https://doi.org/10.1111/j.1749-6632.2009.05093.x
Subsarcolemmal mitochondrial flashes induced by hypochlorite stimulation in cardiac myocytesFree Radical Research 48:1085–1094.https://doi.org/10.3109/10715762.2014.932114
Central role of mitofusin 2 in autophagosome-lysosome fusion in cardiomyocytesJournal of Biological Chemistry 287:23615–23625.https://doi.org/10.1074/jbc.M112.379164
Richard P HarveyReviewing Editor; Victor Chang Cardiac Research Institute, Australia
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Thank you for submitting your article "Mitochondrial Flashes Regulate ATP Homeostasis in the Heart" for consideration by eLife. Your article has been favorably evaluated by Marianne Bronner (Senior Editor) and three reviewers, one of whom is a member of our Board of Reviewing Editors.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
This study investigates the role of mitochondrial flashes in regulating the ATP set-point in the cardiac muscle cells. The results show that the frequency of mitoflashes is negatively correlated with the ATP production and serves as a key regulator for maintaining the balance of ATP supply-demand. The results show that the BCl-xL-regulated proton leakage through F1Fo-ATP synthase appears to mediate the coupling between mitoflash production and the ATP set-point regulation. It is concluded that mitoflashes constitute a digital auto-regulator for ATP homeostasis in the heart.
This is a very important study because it is bringing in a novel concept to explain one of most fundamental questions in bioenergetics, namely, regulation of ATP set-point in beating heart. The authors have applied different approaches to validate their hypothesis. However, there are several major concerns as listed below that either require further explanations or additional experiments. While the authors provide evidence that mito flashes vary according to the interventions applied, the authors have not provided convincing evidence that the mito flashes are setting the ATP homeostasis. Rather mito flashes may be a consequence of alterations in proton flow or proton leak rather than a regulator of ATP production. Furthermore, mito flashes do not occur in every mitochondria suggesting that mito flashes are not playing a significant role in ATP homeostasis. In addition, further experimentation is need to understand the role that calcium plays in frequency of mitoflashes.
1) The ATP measurements in the isolated mitochondria were done in mitochondria suspensions, however, the mitoflash events occurred randomly in only a very small subset of mitochondria (26 ± 2 events / 1000 µm2·100s). The justification for correlating these two measurements was not explained (whole populations of mitochondria vs. a relatively small number of mitochondria).
2) Figure 2C shows the correlation of ATP/ADP, ATP, and flashes. As indicated, glucose-to-pyruvate switch leads to an initial overshoot of mitoflash frequency that coincides with a transient increase of luciferin luminescence (ATP increase), which does not indicate a clear "negative" correlation. Please clarify.
3) Figure 3 used super-high levels of pyruvate, which already significantly increased (many folds) flashes (shown in Figure 2B). It is therefore not clear how the pacing induced suppression of this very high level of flashes has any physiological relevance.
4) Also in Figure 3, manipulations that significantly suppressed the super-high level of flashes did not change ATP levels. This does not support the correlation?
5) Figure 4 is confusing, since the manipulations of flashes through antioxidants may exert other effects to alter the detection/measurement of ATP using the fluorescent indicator. The authors need to rule out that the negative correlation was not a result of indirect effect or off-target effect.
6) Figure 5 is the key data to support this study's conclusion. The idea that BCl-XL coupled but not UCP coupled proton leak triggers flashes (and suppressed ATP) is interesting. However, the authors need to show with direct measurements that manipulating UCP or BCl-XL changes the pH in the microdomain in the matrix near the inner membrane of mitochondria in cardiomyocytes. They also need to explain why and how the leaked protons between these two mechanisms could have a different effect in triggering flashes.
7) What happens to mito membrane potential during the interventions applied and when mitoflashes appear?
8) What happens to the frequency of mito flashes after application of the ATP synthase inhibitor oligomycin?
9) The authors argue that calcium does not regulate the appearance of mito flashes. What effect does inhibition of MCU have on mito flashes? Why does pyruvate which feeds the TCA cycle (a calcium dependent process) increase mito flashes while a calcium chelator also increases mito flashes by 48% (subsection “Mitoflash Response to Altered Energy Expenditure”, last paragraph; Figure 3D)?
10) If the authors argue that mitoflashes regulate ATP, what are the circumstances that "mitoflashes are biomarkers of mito respiration" as mentioned by the authors in the manuscript and argued by others? Why different roles?
11) Since mitoflashes do not occur in all mitos is this a consequence of alterations in mito biogenesis? Do they occur in the mitos undergoing autophagy or undergoing fission?
12) The authors state…"Remarkably, the cellular ATP content and ATP/ADP ratio were held constant regardless of pacing at different frequencies (Figure 3C), substantiating the tightness of the ATP set-point regulation" but this statement seems in contradiction of mito flashes setting the ATP level if pacing results in a decrease in mito flashes. Please clarify.
[Editors' note: further revisions were requested prior to acceptance, as described below.]
Thank you for resubmitting your work entitled "Mitochondrial Flashes Regulate ATP Homeostasis in the Heart" for further consideration at eLife. Your revised article has been favorably evaluated by Marianne Bronner (Senior Editor), a Reviewing Editor, and two reviewers.
The manuscript has been improved but there are some remaining issues that need to be addressed before acceptance, as outlined below:
The authors have made a good effort in addressing the previous concerns. Overall, this study deals with a fundamental question regarding the ATP set-point regulation in beating heart. The data indeed give a strong correlation that mitoflash could be a digital auto-regulator for ATP homeostasis in the heart. Before publication, however, there are still issues concerning the physiological relevance and the causal relationships. There exist several key discrepancies that will require the authors' further consideration. In addition, one reviewer may have overlooked the technical issue last time for flash measurement during pacing (see below). It is candidly felt that the authors should not over interpret their data.
1) The results in Figure 5—figure supplement 2 showing that inhibiting MCU with Ru360 did not show any significant effect on mitoflash frequency, which are in contradictory with two recent publications by several key authors in this manuscript. They have previously shown that blocking mitochondrial Ca2+ transport by knockdown of MICU1 or MCU, markedly diminished the flash response (PMID: 23283965), consistent with the idea that Ca2+ triggers mPTP, the underlying mechanisms for mitoflash. In addition, they have also shown that inhibition of MCU activity by ruthenium red (RR) or by genetic disruption with siRNAs, both significantly depressed superoxide flashes induced by μM [Ca2+]c in permeabilized cells. Specifically, RR decreased flash frequency by 73.8%, siMCU-1 by 73.2% and siMCU-2 by 49.1%. These results show that mitoflashes are activated by the steady-state mitochondrial Ca2+ elevation (PMID: 24699914). These crucial discrepancies between the authors own data need to be explained in detail and unequivocally.
2) The pacing mediated decreases in flash frequency are quite interesting and surprising. However, it is in opposition to the results published by Dr. Wang's group in University of Washington (PMID: 25252178). As I can see, the only difference between these two reports is that the current mitoflash data are acquired before, during and after pacing. The frequency during pacing is decreased, and it returned back right after the pacing stopped. This is different from Wang's JMCC paper, in which the flash is measured before and after pacing, but not during pacing. My concern is that a motion artifact (as shown in their Figure 3 the cell continues to beat, shorten, change volume) could affect the recording of mitoflash. This technical issue needs to be addressed. This technical issue will require the authors to perform simple new experiments by recording the mitoflash right before and after the pacing.
3) I am still bothered by the use of 10 mM pyruvate in the majority of the experiments. I understand that this manipulation increases mitoflash frequency approximately 12 times more than when the cells are incubated in the physiological glucose concentrations (Figure 2A), as such, the authors can have a robust mitoflash signal to study. However, this raises the concern about the physiological relevance and the causal relationship of the reported data. This is an important issue because the "artificially" high mitoflash data support a correlation rather than a causal relationship. Please discuss this issue.
4) Another issue, as pointed out in the previous Question#1 that the measurement of ATP (steady state) and flash are on different populations. In fact, the unchanged ATP level during pacing is understandable (Figure 3C). What really matters is the flux (the rate of ATP production). The flux (ATP generation rate) is likely increased when the pacing rates are increased, but this is not determined. For instance, it is well-known that without a dynamic and continuous ATP regeneration, in less than 60 beats, the entire cellular ATP reservoir will be consumed. Therefore, pacing the heart will drop the cellular ATP to a minimal level within a few seconds until the Ca2+-mediated generation of NADH starts to kick in (see Figure 2 of Brandes R & Bers DM, Biophys J, 2002, PMID: 12124250). Therefore, it is hard to use the steady state ATP measurement to show that ATP flux is controlled by flash mechanistically. Please address this issue.
5) The BCl-xL-mediated leak channel proposed by Jonas group (Alavian et al., 2011, Chen et al., 2011) has a peak conductance of 600 pS on average, which should be much higher than the H+ leak channel that is proposed here. Subsequent studies by Dr. Jonas group suggest this channel could be mPTP itself.https://doi.org/10.7554/eLife.23908.023
- Heping Cheng
- Heping Cheng
- Xianhua Wang
- Heping Cheng
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Drs SS Liu, W Wang, MQ Dong, RP Xiao, YM Wang, JC Luo, M Ouyang, and CQ Song for valuable comments, X Wang for the generous gift of SOD2 adenovirus, T Ye for the synthesis of SS31, and IC Bruce and WL Yan for manuscript editing. This work was supported by the National Key Basic Research Program of China (2013CB531200) and the National Science Foundation of China (31130067, 31470811, and 31521062).
Animal experimentation: All procedures were carried out according to the rules of the American Association for the Accreditation of Laboratory Animal Care International and approved by the Animal Care Committee of Peking University accredited by AAALAC International (IMM-ChengHP-1). This investigation conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996).
- Richard P Harvey, Reviewing Editor, Victor Chang Cardiac Research Institute, Australia
- Received: December 5, 2016
- Accepted: May 16, 2017
- Version of Record published: July 10, 2017 (version 1)
© 2017, Wang 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.