Abstract
In mammals, hypoxic stress management is under the control of the Hypoxia Inducible Factors, whose activity depends on the stabilization of their labile α subunit. In particular, the skeletal muscle appears to be able to react to changes in substrates and O2 delivery by tuning its metabolism. The present study provides a comprehensive overview of skeletal muscle metabolic adaptation to hypoxia in mice and in human subjects exposed for 7/9 and 19 days to high altitude levels. The investigation was carried out combining proteomics, qRT-PCR mRNA transcripts analysis, and enzyme activities assessment in rodents, and protein detection by antigen antibody reactions in humans and rodents. Results indicate that the skeletal muscle react to a decreased O2 delivery by rewiring the TCA cycle. The first TCA rewiring occurs in mice in 2-day hypoxia and is mediated by cytosolic malate whereas in 10-day hypoxia the rewiring is mediated by Idh1 and Fasn, supported by glutamine and HIF-2α increments. The combination of these specific anaplerotic steps can support energy demand despite HIFs degradation. These results were confirmed in human subjects, demonstrating that the TCA double rewiring represents an essential factor for the maintenance of muscle homeostasis during adaptation to hypoxia.
Introduction
Despite a number of studies on cell models and on human subjects exposed to short and long term hypoxia the biochemical mechanisms adopted by muscle tissue to cope with oxygen restriction are not fully understood. Overall, in mammals, hypoxic stress management is under the control of a class of transcriptional activators, the Hypoxia Inducible Factors (HIFs), whose activity depends on the stabilization of their labile α subunit1. In normoxia, the α subunits of HIFs undergo destabilization through hydroxylation by a family of dioxygenases named prolyl hydroxylase domain-containing enzymes (Phds)2. Phd1, 2 and 3 regulate HIFs intracellular levels and specifically, Phd2 act as master regulator of hypoxia response3, 4. HIFs degradation through Phds activity depends primarily on O2 levels, and on α-ketoglutarate (α-KG) and Fe2+ as molecular cofactors, underlining the interdependence between O2 delivery and cellular metabolism2, 5–7. However, HIFs stabilization, regulated by O2 levels, varies according to tissues’ tolerance of hypoxia. In particular, the skeletal muscle reacts to changes in substrates and O2 delivery by tuning its metabolism modulating HIFs. A characteristic of the muscle tissue is its plasticity, defined as the capacity to modulate metabolic pathways in response to changed functional demand under physiological or pathological conditions (i.e. under physical exercise or immobilization)8–13.
Previous proteomic studies conducted on human skeletal muscles exposed to various degrees of hypoxia, indicate that short and long term hypoxia exposures do not permanently activate HIF14, 15. Furthermore, the study of human vastus lateralis muscle exposed to severe hypoxia for 19 and 60 days in the course of the Caudwell Xtreme Everest expedition16 suggested a new mechanism of adaptation to hypoxia, indicating a metabolic TCA cycle rewiring and the use of glutamine as an alternative source for energy production15. Unfortunately, due to the paucity of muscle tissue, enzyme activities and detailed features could not be determined, leaving some aspects of muscle adaptation and particularly the molecular changes associated with the duration of hypoxia exposure, unexplained. To clarify the role of muscle metabolism in hypoxia, animal models represent a valuable source of information that can be translated to human samples17–19 possibly contributing not only to our understanding of the physiological mechanism of human hypoxia adaptation but also to the molecular mechanisms of hypoxia-associated diseases, including cardiovascular and pulmonary disorders and critical illness.
Unexpectedly the activation of HIFs varies in different animal models: HIF is not activated in hearts of mice in acute or chronic exposure20 whereas, rats adapt to acute and chronic oxygen shortage by activating HIF program and increasing anaerobic metabolism21 suggesting that HIFs stabilization, under comparable oxygen exposures, is species dependent22.
The aim of the present study is to provide a comprehensive overview of metabolic adaptation to hypoxia utilizing a mouse model that could reflect the molecular mechanism of hypoxia adaptation of the human skeletal muscle. The investigation was carried out combining proteomic analysis for the primary identification of key factors regulating the complexity of muscle changes under 2- and 10-day hypoxia and mRNA transcripts analysis, by qRT-PCR, followed by protein detection by antigen antibody reactions. Results from the mouse model were verified on protein extracts from human healthy subjects enrolled in previous independent studies14–16 and exposed to hypoxic conditions for 7/9 days at the Margherita Hut, Mt. Rosa (4,559 m a.s.l.), and for 19 days at the Mt. Everest base camp (5,300 m a.s.l.), respectively. The results demonstrate that both mice and human subjects exposed to hypoxia utilized the TCA cycle rewiring to cope with oxygen deficiency introducing for the first time in mammals an alternative use of the TCA cycle to specifically sustain energy production under conditions of limited oxygen availability. These results highlight the capacity of the human body to utilize unconventional metabolic pathways to sustain energy demand and maintain tissue homeostasis.
Results
HIF-1α and HIF-2α signalling
HIF-1α was quantified in total extracts from gastrocnemius muscle of normoxic (N), 2-day hypoxic (2 H) and 10-day hypoxic (10 H) mice. No changes in HIF-1α protein levels were detected in skeletal muscle (Fig. 1A). HIF-1α mRNA expression increased in 2 H only (Fig. 1C).
HIF-2α protein and mRNA were significantly increased in 10 H (Fig. 1B and D) whereas a similar pattern of change, but of lesser magnitude, did not reach statistical significance in 2 H.
Energy sensing and energetic metabolism regulators
Energy sensing was assessed by monitoring the level of phosphorylated (active) form of AMP-activated protein kinase (pAMPK) in relation to the total (AMPK). Metabolic reprogramming in response to glucose and fatty acid availability was assessed by monitoring the level of peroxisome proliferator-activated receptor-gamma coactivator 1α (PGC1α).
The pAMPK/AMPK ratio increased, whereas PGC1α decreased, in both 2 H and 10 H skeletal muscles (Fig. 2, panel A).
The mRNA expression of serine/threonine-protein kinase mTOR and AMPK significantly increased specifically in 2 H skeletal muscle, whereas serine/threonine-protein kinase STK11 (LKB1) significantly increased in both 2 H and 10 H skeletal muscles; the increase in 2 H skeletal muscle was significantly higher than that observed in 10 H (Fig. 2, panel B).
Skeletal muscle proteome profile
The proteome profiles of skeletal muscles from N, 2 H and 10 H were obtained through 2D-DIGE analysis and ESI MS/MS mass spectrometry.
Fifty-one spots were significantly changed comparing 2 H versus N skeletal muscle; conversely 70 spots were significantly changed comparing 10 H vs. N and 38 comparing 2 H vs. 10 H skeletal muscles. Overall, 42% of the identified spots were metabolic enzymes, while the remaining 58% included structural, myofibrillar, stress response and other proteins pertaining to a variety of cellular processes.
The identified metabolic proteins are illustrated in the representative proteomics maps in the Supplementary Fig. S1 and listed in Supplementary Table S1 with the corresponding UniProtKB accession numbers, cellular function, degree of variation expressed as average ratio and detailed mass spectrometry data.
Proteomic results indicate that protein dysregulation took place in three major cell compartments: metabolism, antioxidant proteins and cytoskeletal re-organization.
Cell metabolism
The expression levels of metabolic enzymes involved in energy transfer, glycogen metabolism, glycolysis and tricarboxylic acid (TCA) cycle were altered in both 2 H and 10 H (Fig. 3A).
Decrement of two proteoforms of creatine kinase M-type (Ckm) (−39%, −31%) characterized 2 H only, whereas decrement in glycogen utilization and glycolysis was a common feature of 2 H and 10 H. Specifically, glycogen phosphorylase (Pygm) decreased in 2 H (four proteoforms: −37%, −43%, −34%, −24%) and in 10 H (three proteoforms: −34%, −37%, −26%); phosphoglucomutase 2 (Pgm2) changed in 2 H (one proteoform increased, +32%, another one decreased, −34%) and in 10 H (−33%). In addition, several proteoforms of β-enolase (Eno3) decreased in both 2 H (−36%, −28%, −27%) and 10 H (−33%, −23%) as well as pyruvate kinase (Pkm) that was decreased by 30% under both conditions.
With regards to aerobic metabolism, NADH-ubiquinone oxidoreductase 75 KDa subunit (Ndufs1, 13%), succinate dehydrogenase flavoprotein (Sdha, 17%), ATP synthase subunit beta (Atp5b, 15%), and the cytoplasmic malate dehydrogenase (Mdh1, 19%) were increased in 2 H, whereas aconitate hydratase was decreased (Aco2, −25%). By contrast, in 10 H, Ndufs1 (−16%), Sdha (−18%), three proteoforms of Aco2 (−30%, −27%, −31%), the subunit alpha of mitochondrial isocitrate dehydrogenase 3 (Idh3, −36%), two proteoforms of 2-oxoglutarate dehydrogenase (Ogdh, both proteoforms −21%) and two proteoforms of dihydrolipoyl dehydrogenase (Dld, both proteoforms −28%) decreased.
Structural/contractile and antioxidant defense molecules: proteomic results
Cytoskeletal remodelling (Fig. 3B) was suggested by a decrease of tubulin beta-2C chain (Tubb4) and vimentin (Vim) in 10 H, whereas desmin (Des) was decreased in both 2 H and 10 H.
Concerning contractile proteins: myosin-4 (Myh4) decreased in both conditions. Tubb4b, troponin T fast (Tnnt3), tropomyosin beta chain (Tpm2), myosin light chain 1/3, skeletal muscle isoform (Myl1) increased in 2 H, whereas myosin-binding protein H (Mybph) and myosin light chain 3 (Myl3) increased in 10 H.
Importantly, protein disulfide-isomerase (P4hb) decreased both in 2 H and 10 H. Protein disulfide-isomerase A3 (Pdia3), tripartite motif-containing protein 72 (Trim72), stress response protein HSP 90-beta (Hsp90ab1) and heat shock cognate 71 kDa protein (Hspa8) decreased in 10 H, whereas protein DJ-1 (Park7) increased.
Other proteins
Carbonic anhydrase 3 (Ca3) increased in 10 H and decreased in 2 H, whereas myoglobin (Mb) increased in 10 H and parvalbumin alpha (Pvalb) increased in 2 H and 10 H. The mitochondrial elongation factor Tu (Tufm) and Immt protein (Immt) decreased in 10 H, whereas fibrinogen beta chain (Fgb), fibrinogen gamma chain (Fgg), serotransferrin (Tf), and serum albumin (Alb) decreased in both conditions (Fig. 3B).
Citrate utilization
Citrate can be transported from mitochondria to cytoplasm to produce acetyl-CoA for fatty acid synthesis and oxaloacetate or, alternatively, it can be a substrate for α-ketoglutarate (α-KG) production through the cytosolic isocitrate dehydrogenase 1.
α-KG is a key metabolite being both a substrate for HIF prolyl hydroxylases and a precursor for glutamate production, which in turn can be utilized for glutamine and glutathione synthesis.
The expression levels of fatty acid synthase (Fasn), isocitrate dehydrogenase 1 (Idh1), HIF prolyl hydroxylases 2 and 3 (Phd2 and Phd3), l-glutathione synthetase and glutamine synthetase (Glns and Gss) were evaluated by immunoblotting, in skeletal muscle (Fig. 4). In 2 H, Fasn was decreased whereas an increment was observed for Idh1, Glns, Gss and Phd2. Conversely, in 10 H, the expression level of Fasn was markedly increased, while Idh1 was decreased. Glns and Gss remained increased compared to normoxic controls, Phd3 increased whereas Phd2 appeared normalized.
Beside fatty acid synthesis, citrate can generate cytosolic oxaloacetate. In a non-gluconeogenetic tissue such as muscle, oxaloacetate can be used through anaplerotic malate production by the cytosolic malate dehydrogenase (Mdh1). Cytosolic malate can be reimported into mitochondria and interconverted by mitochondrial malate dehydrogenase (Mdh2), fumarase and succinate dehydrogenase, refueling the TCA cycle. Proteomic data indicated a slight increment of Mdh1, succinate dehydrogenase A chain (Sdha), NADH ubiquinone oxidoreductase 75 KDa (Ndufs1) and ATP synthase beta (Atp5b) in 2 H and a decrement of Ndufs1 and Sdha in 10 H, in spite of a decrease of mitochondrial isocitrate dehydrogenase 3 (Idh3) and aconitate hydratase (Aco2) in both conditions (Fig. 3A). To demonstrate the use of this alternative pathway to produce energy, the expression levels of Mdh2 and Sdha were assessed by antigen antibody reactions (Fig. 4). Results showed a trend to increase in 2 H, and a statistically significant decrement in 10 H that confirmed proteomic data.
Concerning the respiratory chain, complex I and II activities were increased in 2 H compared with N, whereas complex III remained unchanged. In 10 H, complex I and II were unchanged with respect to controls and complex III increased. Citrate synthase activity remained unchanged in both 2 H and 10 H vs. N (Fig. 5).
Hexosamine pathway
Since the activation of glutamine synthetase and the restriction of α-KG flux through the TCA were observed, it can be postulated that glutamine is available either as substrate precursor or for the hexosamine pathway.
The hexosamine biosynthetic pathway (HBP) is considered a sensor for the nutritional state of the cell, as this metabolic pathway integrates glucose, glutamine, fatty acids and uridine. It provides UDP-N-acetylglucosamine (UDP-GlcNAc), the monosaccharide donor molecules for O-GlcNAcylation or N-glycosylation. The latter is necessary for ER homeostasis and contributes to protein tertiary structure formation and protein sorting to achieve proper protein folding in the ER. Disruption of this glycosylation leads to the accumulation of unfolded proteins in the ER lumen and induces the unfolded protein response (UPR)23. The HBP relies on glucose and glutamine uptake.
Fructose-1,6-bisphosphatase (Fbp1) was unchanged, both in 2 H and 10 H conditions. In 2 H, the HBP pathway analysis indicated glucosamine 6-phosphate N-acetyltransferase (Gna1) similar to normoxic control whereas UDP-N-acetylhexosamine pyrophosphorylase (Uap1) was increased. Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit STT3B (Stt3b) was unchanged, whereas UDP-N-acetylglucosamine-peptide N-acetylglucosaminyltransferase 110 kDa subunit (Ogt) and protein O-GlcNAcase (Oga) were decreased. In 10 H, Gna1 decreased whereas Uap1 and Ogt were normalized. Stt3b and Oga were decreased (Fig. 6).
These results suggest that glutamine in 2 H can be utilised for UDP-N-acetylglucosamine synthesis whereas in 10 H it might become available for anabolic substrate production or glutathione synthesis.
Autophagy
Cytoskeletal remodelling is associated with the activation of the autophagic process to clear damaged proteins. Immunoblottings indicated that the energy costly process of autophagy was increased as suggested by the increase of BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 (Bnip3) level both in 2 H and 10 H. The lipidated (activated) form of microtubule-associated protein 1 light chain 3 beta (LC3B-II) was increased in 2 H and normalized in 10 H. The levels of Beclin1 (Becn1) and apoptosis regulator Bcl2 were unchanged, both in 2 H and in 10 H (Fig. 7A). These results were confirmed also at transcript level, with the exception of Becn1 mRNA, which was upregulated in both conditions. qRT-PCR indicated that microtubule-associated protein 1 light chain 3 alpha (LC3A), LC3B and Bnip3 increased in 2 H whereas Becn1, apoptosis regulator Bax and BCL2/adenovirus E1B 19 kDa interacting protein 3-like (Bnip3L) increased both in 2 H and 10 H (Fig. 7B).
Rewiring of the TCA cycle in human skeletal muscle exposed to 7 to 9 days and 19 days severe hypoxia
Markers of TCA rewiring, detected in 2 H and 10 H mice, were also determined in human skeletal muscle exposed to either 7 to 9 days hypoxia (Angelo Mosso laboratory, Margherita Hut, Mt. Rosa Italy, 4,559 m a.s.l.) or 19 days hypoxia (at the Everest base camp, Mt. Everest, 5,300 m a.s.l.) and are represented in Fig. 8. Results indicated non-significant changes in citrate synthase protein level after both exposures, a significant down regulation of Aco2 in both conditions, an increment of Sdha after 7 to 9 days exposure and a down regulation after 19 days at the Everest base camp. Idh1 and Mdh2 were increased after 7 to 9 days, whereas they were unchanged and decreased respectively, after 19 days at the Everest base camp. Fasn did not change significantly after both exposures. These results confirm the role of TCA cycle rewiring in adaptation to hypoxia and its dependency on the duration of hypoxia exposure.
Discussion
This study addresses the role of TCA cycle during hypoxia adaptation of the skeletal muscle tissue in rodents and validates the results in human muscles.
In mice, the activity of Phds inhibits HIF-1α stabilization both in 2 H and 10 H, whereas HIF is active only in 10 H in which HIF-2α is increased, suggesting that metabolic adaptation is at variance with that observed in severely hypoxic cell cultures1, 24–26.
In muscle under physiological conditions, the response to energy demand is controlled by AMPK, whose activity increases during metabolic stress conditions induced by cellular ATP restriction. Upon activation, AMPK increases cellular energy levels by inhibiting anabolic energy consuming pathways (fatty acid synthesis, protein synthesis, etc.) and stimulating catabolic pathways (fatty acid oxidation, glucose transport, etc.). Furthermore, PGC1α stimulates mitochondrial biogenesis and promotes muscle tissue remodelling toward a more oxidative and less glycolytic fiber-type composition, and participates in the regulation of both carbohydrate and lipid metabolism27. Our results indicate that, despite AMPK signalling, in mice, PGC1α decreased in both 2 H and 10 H. These changes were observed also in the heart muscle exposed to the same hypoxia protocol in a previous study20. We believe that this profile is a transient state that precedes the activation of genes under HIFs control. This is possible due to the energy saving mechanisms since, by inhibiting PGC1α, the energy-costly process of the mitochondrial biogenesis is reduced. This phenomenon appears robust and characteristic of the early phase of adaptation to hypoxia, preceding HIFs activation and being associated to macroautophagy onset28. Autophagy can also explain the increment of respiratory chain complexes observed in the early stage. This event has been described also in hypoxic fibroblasts cultures29. In the presence of autophagy, the dysfunctional proteins are degraded, thus enzyme levels are reduced, despite their activities preserved. This can occur because the fusion and fission processes, at mitochondrial level, segregate and selectively discard damaged mitochondrial components, enriching the remaining mitochondria with undamaged material and thus contributing to the maintenance of the bioenergetics efficiency of the muscle cell30, 31. These results do not provide sufficient information on the energetic status of the tissue and on its adaptation to hypoxia. However, their integration with the proteomic analysis of primary metabolism, cytoskeletal remodelling and stress response, contributes to go better insight into both questions.
In the context of muscle energy demand, the tricarboxylic acid (TCA) cycle represents the metabolic link between carbohydrates, lipids, aminoacid oxidation and ATP production through oxidative phosphorylation. The metabolic profile of hypoxic skeletal muscle was characterized by lower expression levels of creatine kinase (Ckm) and of enzymes belonging to the glycogen metabolism (Pygm, Pgm2), glycolysis (Eno3, Pkm) and TCA cycle (Aco2, Idh3a, Ogdh, Dld), both in 2-day and in 10-day severe hypoxia. It is noteworthy that the drop of Ckm, involved in glycogen metabolism, and of the TCA cycle, is a common feature of human subjects exposed to short and long term extreme altitude, as described in previous proteomic differential studies of hypoxia adaptation14, 15. These studies indicated a decreased level of glycolytic enzymes in contrast with results on cultured cells or in rats under severe hypoxia24, 32.
The cause of hypoxic skeletal muscle harm has been mainly attributed to ROS production induced by oxidative stress33, 34. Several pieces of evidence have shown that proteins exposed to oxidants like hydrogen peroxide, superoxide, hydroxyl radical and peroxynitrite enhanced proteasomal degradation35. Creatine kinase, glycogen phosphorylase and pyruvate kinase as well as the ryanodine receptor 136 were described as targets of oxidation of Cys residues and nitration37. In the present context, the role of mitochondrial ROS affecting calcium handling proteins involved in contractility, described in animal model36, can be associated to muscle mass loss observed in Caucasian exposed to high altitude38, 39.
Also, mitochondrial aconitate hydratase (Aco2) was under expressed both in 2- and 10-day severe hypoxia. This enzyme has been reported as being particularly susceptible to ROS-mediated inhibition40, 41 and, subsequently, to proteolytic degradation after oxidative modification. Aco2 decrement was also observed in previous studies of hypoxia adaptation in animal models21 and in the vastus lateralis muscle of humans exposed to hypobaric hypoxia14. It can be hypothesized that under-expression of the above-described molecules could be due to impaired translation or enhanced protein degradation to support the amino acid pool. Further investigations, addressing these aspects, are in progress.
Concerning Mdh2 and Sdha, the increased levels in 2 H and decreased levels in 10 H, assessed by immunoblotting, confirm proteomic data and suggest that the reverse TCA cycle utilizes citrate synthase to convert citrate into oxaloacetate and acetyl-CoA in 2 H, whereas in prolonged hypoxia lipid metabolism plays a prominent role.
To support TCA cycle rewiring, NADH is an essential cofactor and it can become available through a cytosolic accumulation mediated by enolases and pyruvate kinase decrement. The latter, by decreasing the availability of pyruvate, blunts its transformation to lactate, and thus the oxidation of NADH to NAD+, leaving the substrate available for cytoplasmic malate dehydrogenase. The resulting cytosolic malate can be reimported into mitochondria, thus refueling the TCA cycle.
Previous studies have indicated that during the transition from a short-term to prolonged hypoxia (i.e. Mt. Everest Pyramid, 5,400 m a.s.l.) human subjects, performing maximal exercise at high altitude, acutely exhibit reduced levels of blood lactate, that renormalize after a long stay at altitude. This unexpected transient phenomenon has been termed the “lactate paradox”42–44. Taking into consideration that mice have a five to seven-fold faster specific metabolic rate than humans, in our experimental conditions, lactate is not produced since enolases are decreased and NADH is utilized to support malate and succinate synthesis, and it is transient since the metabolic rewiring reflects the early phase of adaptation only. Further study, based on metabolomics analysis, could be useful to determine metabolites associated with the above-described TCA rewiring: these molecules, can be considered putative biomarkers for clinical monitoring of diseases associated with oxygen deprivation that occurs when patients experience intermittent hypoxia, such as in sleep apnoea syndrome45.
To sustain the metabolic demand, the first TCA rewiring occurs in mice in 2 H and is mediated by cytosolic malate whereas the second rewiring occurs in 10 H and is mediated by Idh1 and Fasn, supported by glutamine and HIF-2α increments. It is known that, under hypoxic stress, mitochondrial lipid oxidation is reduced in favor of lipid storage46, 47 and this process is modulated by the action of HIF-2α48. In humans, the first rewiring is observed after 7/9 days of hypoxia exposure whereas the second rewiring is revealed after 19 days of oxygen restriction. Our results also indicate a role for glutamine in the 10 H phase of adaptation. Glutamine, exerts many important metabolic functions49 like anaplerosis50 or de novo lipogenesis via a reductive metabolism51, 52. Since skeletal muscle is the main site of glutamine production as well as the major contributor to whole-body glutamine supply53, it is clear that effective glutamine synthesis contributes to ensure nutrient provision, anti-inflammatory and anti-oxidative responses, not only to muscular function54, 55. Our results indicate that glutamine could become available as an anabolic precursor of UDP-N-acetylglucosamine, as indicated by Uap1 upregulation in 2 H, or generate de novo lipogenesis utilizing the anaplerotic cycle trough Idh1 in 10 H.
This observation in 10 H is supported by the increment in fatty acid synthase (Fasn) that is a common outcome of prolonged hypoxia exposure in human skeletal muscle. Fasn uses products of the TCA cycle to synthesize the saturated fatty acid palmitate, contributing to de novo lipogenesis.
Overall, it can be concluded that in the early phase of adaptation muscle tissue utilizes recycled malate to refuel the TCA in mice and this is confirmed in human subjects exposed to 7/9 days hypoxia, whereas after 10 days in mice and 19 days in humans, a central role of glutamine can be postulated.
Concerning prolyl hydroxylase domain containing enzymes, it is known that both enzymes contribute to the HIF system regulation with different substrate specificity, Phd2 being more active towards HIF-1α and Phd3 towards HIF-2α3, 56. Here we confirmed the induction of Phd2 and Phd3 in skeletal muscle under 2-day hypoxia only. Their inducible behavior presumably reflects the tissue flexibility in regulating HIF-dependent response to hypoxia and this response is modulated in a time-dependent manner.
Another element, clearly disclosed by the present study, is the cytoskeletal re-arrangement that can be associated to autophagosome formation enhancing the protein quality control thus preserving tissue homeostasis and preventing ER stress23.
Our data suggest that the autophagic activation observed in 2 H is sustained by the metabolic rewiring that utilizes cytosolic malate dehydrogenase to refuel the TCA cycle thus maintaining tissue homeostasis. In contrast, the energetic status of 10 H cannot support autophagosome formation, being energy production impaired. These results provide a link among autophagic impairment, cytoskeletal remodelling and TCA cycle rewiring, to muscle homeostasis disruption17–19. For the first time this study identifies a modified TCA rewiring system in human and mouse muscles. These results could contribute to improve the understanding of the metabolic adaptation occurring in pathological conditions, including sleep apnea, cardiovascular and pulmonary disorders and critical illness.
Nevertheless we are aware that the small sample size and the absence of an independent replication for more confident statistics, besides the inability of 2D-DIGE to identify species under 125 picomoles, represent a major limitation of this study. More efforts should be implemented to increase the number of samples, recruiting not only healthy subjects exposed to low oxygen levels but also patients characterized by comparable hypoxic conditions, like sleep apnea syndrome, cardiovascular and pulmonary insufficiency. The validation step is essential to support the proposed adaptive molecular mechanism, overcoming eventual statistical bias and the contribution of confounding effects.
Overall Conclusions
From the present study, it can be hypothesized that citrate, generated by pyruvate and the reductive TCA cycle, driven by cytosolic Idh1, could be utilized to produce ATP for energetic support. This occurs through an alternative pathway that utilizes the cytosolic malic enzyme to produce malate. These results suggest that the combination of two specific anaplerotic steps can support energy demand despite HIFs degradation, activating sophisticated mechanisms, including ROS signaling and autophagy, specific for tissue preservation. Interestingly, this mechanism is active in 2 H not in 10 H, where adaptation occurs by increasing fatty acid oxidation as indicated by Fasn increment and Idh1 decrement.
Overall these results suggest a direct interplay between ROS production and the double TCA cycle rewiring in which ROS may act as signalling molecules in concert with the metabolic rewiring, supported by a fine quality control exerted by autophagy.
These aspects should be considered in the frame of adaptive cell hypoxia, a transient phenomenon in which compensatory mechanisms sustain metabolism and energy utilization, in a changing environment34, 57. Mitochondrial ROS formation can be considered a potential effector of such a sensing system58. Low Po2 and high OXPHOS complexes levels, make electrons more available for reduction reactions (e.g. the reduction of O2 to superoxide), enhancing ROS production and triggering cell signaling to keep the energy demand at lower levels.
In conclusion, in 2-day hypoxia, cytosolic citrate is utilized for glutamine, glutathione and α-KG production to promote HIF prolyl hydroxylases activity and to sustain muscle adaptation to hypoxia. Conversely, after 10-day exposure cytosolic citrate is diverted to fatty acids biosynthesis (see Fig. 9). Importantly, these results are confirmed in human subjects exposed for 7/9 and 19 days, respectively, to severe hypoxia, demonstrating that the TCA double rewiring is also active in human subjects and represents an essential factor for the maintenance of muscle homeostasis during adaptation to hypoxia.
Methods
Animals
Mice were divided into three groups: controls, normoxic mice (N, n = 5), which breathed room air (FIO2 = 0.21), mice exposed for 48 h to normobaric hypoxic atmosphere (FIO2 = 0.08) (2 H, n = 5) and mice which were subjected to the same treatment as 2 H, but for 10 days (10 H, n = 5). The hypoxic chamber incorporated a compensation unit to prevent any exposure of animals to room air during feeding, cleaning operations and sacrifice59. For sacrifice, animals were transferred to the compensation chamber, which was continuously flushed with the hypoxic gas, and anesthetized with a hip injection of sodium thiopental (10 mg/100 g body wt) and heparin (500 units). Skeletal muscles were removed soon after the sacrifice (less than 1 min), immediately frozen in liquid nitrogen and then stored at −80 °C until use. The investigation was carried out in accordance with 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). All experimental protocols were approved by the University of Milan ethical committee.
Human biopsies
The participants were: (a) healthy volunteers recruited from the investigators group of the Caudwell Xtreme Everest 2007 research expedition to Mount Everest of the University College London (UCL), UK15, 16 or (b) members recruited by the Margherita Hut Scientific Committee at the University of Torino (UNITO), Italy14. Written informed consent was obtained from all participants. Protocols were approved by the UCL research ethics committee and the UNITO Ethical Committee in accordance to the World Medical Association Code of Ethics, Declaration of Helsinki (1964). Baseline skeletal muscle biopsies were taken from both groups prior to departure. Members of a) had a repeat biopsy taken on expedition day 19 (6 days after arrival at the Everest Base Camp, Mt. Everest, 5,300 m a.s.l.), whereas members of b) had a repeat biopsy taken over days 7–9 (3 days after arrival at the Angelo Mosso laboratory, Margherita Hut, Mt. Rosa, 4,559 m a.s.l.). Biopsies were taken from the mid part of the vastus lateralis muscle. A part of each biopsy (5–10 mg) was snap-frozen and maintained in liquid nitrogen until analysis in Milan.
Protein extraction
Two-dimensional differences in gel electrophoresis (2D-DIGE) and immunoblots: an aliquot of each frozen muscle was suspended in lysis buffer (urea 7 M, thiourea 2 M, CHAPS 4%, Tris 30 mM, and PMSF 1 mM) and solubilized by sonication on ice. Proteins were selectively precipitated using PlusOne 2D-Clean-up kit to remove non-protein impurities and re-suspended in lysis buffer. Protein extracts were adjusted to pH 8.5 by the addition of NaOH 1 M solution, and sample concentrations were determined using PlusOne 2D-Quant kit.
Enzymatic activities: 30–50 mg of frozen muscle were diluted 1:20 (wt/vol) in ice-cold sucrose muscle homogenization buffer (Tris 20 mM, KCl 40 mM, EGTA 2 mM, Sucrose 250 mM, pH 7.4) and homogenized in a glass-glass tissue grinder. Muscle homogenates were centrifuged at 600 g for 10 min at 4 °C. Supernatants were immediately assayed for enzymatic activities. Total protein quantitation was determined using PlusOne 2D-Quant kit.
Proteomic analysis
Protein labeling, 2D separation and analysis were performed as previously described20. The proteomic profile of each group of hypoxic mice was compared with the normoxic group. Statistically significant differences of 2D-DIGE data were computed by an independent one-way analysis of variance (ANOVA) coupled to Tukey’s multiple-group comparison test (p < 0.01). Normality of data distribution was assessed by applying the Shapiro-Wilk test. False discovery rate was applied as multiple test correction in order to keep the overall error rate as low as possible. Statistically changed spots were further filtered on the basis of the average ratio value provided by DeCyder 2D software: only spots with an average ratio >1.1 or <−1.1 were considered as differentially expressed.
Proteins were identified by matrix-assisted laser desorption/ionization time of flight utilizing the method previously described20.
Identified proteins are indicated in representative proteomics maps in Supplementary Fig. S1. Detailed proteomics and mass spectrometry data are reported in Supplementary Table S1.
Real time PCR
Total RNA from frozen muscle was extracted by TRIzol Reagent according to the manufacturer’s protocol (Invitrogen) and residual phenol and salts were removed using the PureLink™ Micro-to Midi™ RNA Total RNA Purification System (Invitrogen). RNA quality and dosage were assessed on the Bioanalyzer instrument (Agilent Technologies): the A260/280 ratio and RNA Integrity Number (RIN) were measured. Samples in which RIN value was below 7.0 were unused for this study. About 1 µg of RNA sample was reverse transcribed to cDNA with SuperScriptII reverse transcriptase and oligo(dT) according to manufacturer’s specifications (Invitrogen). Primers for qRT-PCR analysis were designed by the Primer3 software (http:// fokker.wi.mit.edu/primer3) and tested for their mouse specificity using NCBI database. The sequences of the qRT-PCR primer pairs (forward and reverse) used are listed in Supplementary Table S2. The reactions were performed in a 20 µL reaction volume containing 10 pmole of each primer. qRT-PCR was performed with a Fast SYBR Green Master Mix and processed on a 7500 Fast Real-Time PCR System according to manufacturer’s specifications (Applied Biosystems). The following PCR amplification parameters were used: 5 min at 95 °C, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min. The dissociation curve was conducted at the end of each PCR reaction. Quantitative data were analysed by average of octuplicates Ct (Cycle threshold) according to the 2−ΔΔct method and normalized versus housekeeping actB and tbp genes. Data were generated from eight independent experiments and subjected to a an independent one-way ANOVA coupled to Tukey’s multiple-group comparison test (p < 0.05).
Immunoblotting
Protein extracts (50 μg) from hypoxic and control skeletal muscles, were resolved by SDS-PAGE on 6_14% gradient polyacrylamide gels or 12% homogeneous polyacrylamide gels and transferred onto PVDF membranes. MagicMark XP western protein standard (Thermo Fisher Scientific) was loaded in a separate lane as a molecular weight marker (size range: 20–220 KDa). Blots were incubated with rabbit, goat or mouse polyclonal primary antibodies diluted as follows: anti-HIF-1α (Novus Biologicals) 1:1000, anti-HIF-2α (Novus Biologicals) 1:1000, anti-AMPK (Cell Signaling Technology, CST) 1:1000, anti-pAMPK (CST) 1:1000, anti-PGC1α (Santa Cruz Biotechology, SCBT) 1:500, anti Bnip3 (CST) 1:1000, anti-Becn1 (CST) 1:1000, anti-bcl2 (BD transduction labs) 1:1000, anti-LC3B (CST) 1:1000, anti-Fasn (SCBT) 1:80, anti-Idh1 (SCBT) 1:500, anti-Phd2 and 3 (Novus Biologicals) 1:500 and 1:1000 respectively, anti-Glns (SCBT) 1:500, anti-Gss (SCBT) 1:500, anti-Mdh2 (SCBT) 1:500, anti-Sdha (SCBT) 1:500, anti-Fbp1 (GeneTex) 1:1000, anti-Gna1 (SCBT) 1:500, anti-Uap1 (SCBT) 1:500, anti-Stt3b (Proteintech) 1:1000, anti-Ogt (CST) 1:1000, anti-Oga (Sigma Aldrich) 1:1000. Signals were visualized by chemiluminescence by ECL prime detection kit (GE Healthcare). Images were scanned using ImageQuant LAS 4000 mini digital imaging system (GE Healthcare) and each band was quantitated using ImageQuant Software (GE Healthcare). Data were normalized against the total amount of proteins stained by Sypro Ruby and subjected to an independent one-way ANOVA coupled to Tukey’s multiple-group comparison test. Differences were considered significant at p < 0.05.
Enzymatic activity assay
Citrate synthase and respiratory chain complexes I, II, and III activities were assessed following thoroughly the method described by M. Spinazzi et al.60.
Electronic supplementary material
Acknowledgements
This work was supported by the Italian Ministry of Education, University and Research (MIUR), grant FIRB RBRN07BMCT and PRIN 2015FBNB5Y to CG, by the European Community’s Seventh Framework Program (FP7/2007–2013), grant agreement n. 241665 (BIO-NMD) and by Italian Federation of Sport Medicine, CONI, Rome, Italy. Authors are grateful to Prof. Carsten Lundby, at the University of Zurich, Center for Integrative Human Physiology, for having provided human sample biopsies. The authors thank Dr. Antonia Orsi, at Salupont Consulting Ltd., for manuscript revision.
Author Contributions
D.C.: immunoblotting, data analysis and manuscript preparation. A.V., M.M.: 2-D DIGE experiments. E.T., C.F.: mass spectrometry. V.B.: real time PCR analyses. M.S., A.C.: provided muscle tissue from hypoxic mice. D.L., M.G., P.C.: provided human biopsies, manuscript review. C.G.: study design, data analysis, manuscript preparation.
Competing Interests
The authors declare that they have no competing interests.
Footnotes
Electronic supplementary material
Supplementary information accompanies this paper at doi:10.1038/s41598-017-10097-4
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Semenza GL. Oxygen sensing, hypoxia-inducible factors, and disease pathophysiology. Annual review of pathology. 2014;9:47–71. doi: 10.1146/annurev-pathol-012513-104720. [DOI] [PubMed] [Google Scholar]
- 2.Kaelin WG, Jr., Ratcliffe PJ. Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway. Molecular cell. 2008;30:393–402. doi: 10.1016/j.molcel.2008.04.009. [DOI] [PubMed] [Google Scholar]
- 3.Appelhoff RJ, et al. Differential function of the prolyl hydroxylases PHD1, PHD2, and PHD3 in the regulation of hypoxia-inducible factor. The Journal of biological chemistry. 2004;279:38458–38465. doi: 10.1074/jbc.M406026200. [DOI] [PubMed] [Google Scholar]
- 4.Berra E, et al. HIF prolyl-hydroxylase 2 is the key oxygen sensor setting low steady-state levels of HIF-1alpha in normoxia. The EMBO journal. 2003;22:4082–4090. doi: 10.1093/emboj/cdg392. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Epstein AC, et al. C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell. 2001;107:43–54. doi: 10.1016/S0092-8674(01)00507-4. [DOI] [PubMed] [Google Scholar]
- 6.Fandrey J, Gorr TA, Gassmann M. Regulating cellular oxygen sensing by hydroxylation. Cardiovascular research. 2006;71:642–651. doi: 10.1016/j.cardiores.2006.05.005. [DOI] [PubMed] [Google Scholar]
- 7.Siddiq A, Aminova LR, Ratan RR. Hypoxia inducible factor prolyl 4-hydroxylase enzymes: center stage in the battle against hypoxia, metabolic compromise and oxidative stress. Neurochemical research. 2007;32:931–946. doi: 10.1007/s11064-006-9268-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Ferraro E, Giammarioli AM, Chiandotto S, Spoletini I, Rosano G. Exercise-induced skeletal muscle remodeling and metabolic adaptation: redox signaling and role of autophagy. Antioxidants & redox signaling. 2014;21:154–176. doi: 10.1089/ars.2013.5773. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Hoppeler H, Baum O, Lurman G, Mueller M. Molecular mechanisms of muscle plasticity with exercise. Comprehensive Physiology. 2011;1:1383–1412. doi: 10.1002/cphy.c100042. [DOI] [PubMed] [Google Scholar]
- 10.Moriggi M, et al. Long term bed rest with and without vibration exercise countermeasures: effects on human muscle protein dysregulation. Proteomics. 2010;10:3756–3774. doi: 10.1002/pmic.200900817. [DOI] [PubMed] [Google Scholar]
- 11.Salanova M, et al. Disuse deterioration of human skeletal muscle challenged by resistive exercise superimposed with vibration: evidence from structural and proteomic analysis. FASEB journal: official publication of the Federation of American Societies for Experimental Biology. 2014;28:4748–4763. doi: 10.1096/fj.14-252825. [DOI] [PubMed] [Google Scholar]
- 12.Salanova M, et al. Vibration mechanosignals superimposed to resistive exercise result in baseline skeletal muscle transcriptome profiles following chronic disuse in bed rest. Scientific reports. 2015;5 doi: 10.1038/srep17027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Carson, J. A., Hardee, J. P. & VanderVeen, B. N. The emerging role of skeletal muscle oxidative metabolism as a biological target and cellular regulator of cancer-induced muscle wasting. Seminars in cell & developmental biology (2015). [DOI] [PMC free article] [PubMed]
- 14.Vigano A, et al. Proteins modulation in human skeletal muscle in the early phase of adaptation to hypobaric hypoxia. Proteomics. 2008;8:4668–4679. doi: 10.1002/pmic.200800232. [DOI] [PubMed] [Google Scholar]
- 15.Levett DZ, et al. Changes in muscle proteomics in the course of the Caudwell Research Expedition to Mt. Everest. Proteomics. 2015;15:160–171. doi: 10.1002/pmic.201400306. [DOI] [PubMed] [Google Scholar]
- 16.Levett DZ, et al. Design and conduct of Caudwell Xtreme Everest: an observational cohort study of variation in human adaptation to progressive environmental hypoxia. BMC medical research methodology. 2010;10 doi: 10.1186/1471-2288-10-98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.De Palma S, et al. Muscle proteomics reveals novel insights into the pathophysiological mechanisms of collagen VI myopathies. Journal of proteome research. 2014;13:5022–5030. doi: 10.1021/pr500675e. [DOI] [PubMed] [Google Scholar]
- 18.De Palma S, et al. Changes in muscle cell metabolism and mechanotransduction are associated with myopathic phenotype in a mouse model of collagen VI deficiency. PloS one. 2013;8 doi: 10.1371/journal.pone.0056716. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Grumati P, et al. Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration. Nature medicine. 2010;16:1313–1320. doi: 10.1038/nm.2247. [DOI] [PubMed] [Google Scholar]
- 20.Vigano A, et al. Protein modulation in mouse heart under acute and chronic hypoxia. Proteomics. 2011;11:4202–4217. doi: 10.1002/pmic.201000804. [DOI] [PubMed] [Google Scholar]
- 21.De Palma S, et al. Metabolic modulation induced by chronic hypoxia in rats using a comparative proteomic analysis of skeletal muscle tissue. Journal of proteome research. 2007;6:1974–1984. doi: 10.1021/pr060614o. [DOI] [PubMed] [Google Scholar]
- 22.Bianciardi P, et al. Chronic in vivo hypoxia in various organs: hypoxia-inducible factor-1alpha and apoptosis. Biochemical and biophysical research communications. 2006;342:875–880. doi: 10.1016/j.bbrc.2006.02.042. [DOI] [PubMed] [Google Scholar]
- 23.Palorini R, et al. Protein Kinase A Activation Promotes Cancer Cell Resistance to Glucose Starvation and Anoikis. PLoS genetics. 2016;12 doi: 10.1371/journal.pgen.1005931. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Semenza GL. Transcriptional regulation by hypoxia-inducible factor 1 molecular mechanisms of oxygen homeostasis. Trends in cardiovascular medicine. 1996;6:151–157. doi: 10.1016/1050-1738(96)00039-4. [DOI] [PubMed] [Google Scholar]
- 25.Semenza GL, et al. Hypoxia response elements in the aldolase A, enolase 1, and lactate dehydrogenase A gene promoters contain essential binding sites for hypoxia-inducible factor 1. The Journal of biological chemistry. 1996;271:32529–32537. doi: 10.1074/jbc.271.51.32529. [DOI] [PubMed] [Google Scholar]
- 26.Semenza GL, Wang GL. A nuclear factor induced by hypoxia via de novo protein synthesis binds to the human erythropoietin gene enhancer at a site required for transcriptional activation. Molecular and cellular biology. 1992;12:5447–5454. doi: 10.1128/MCB.12.12.5447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Liang H, Ward WF. PGC-1alpha: a key regulator of energy metabolism. Advances in physiology education. 2006;30:145–151. doi: 10.1152/advan.00052.2006. [DOI] [PubMed] [Google Scholar]
- 28.Zhang H, et al. Mitochondrial autophagy is an HIF-1-dependent adaptive metabolic response to hypoxia. The Journal of biological chemistry. 2008;283:10892–10903. doi: 10.1074/jbc.M800102200. [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
- 29.Baracca A, Sgarbi G, Padula A, Solaini G. Glucose plays a main role in human fibroblasts adaptation to hypoxia. The international journal of biochemistry & cell biology. 2013;45:1356–1365. doi: 10.1016/j.biocel.2013.03.013. [DOI] [PubMed] [Google Scholar]
- 30.Twig G, et al. Fission and selective fusion govern mitochondrial segregation and elimination by autophagy. The EMBO journal. 2008;27:433–446. doi: 10.1038/sj.emboj.7601963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Twig G, Hyde B, Shirihai OS. Mitochondrial fusion, fission and autophagy as a quality control axis: the bioenergetic view. Biochimica et biophysica acta. 2008;1777:1092–1097. doi: 10.1016/j.bbabio.2008.05.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Bergeron M, Yu AY, Solway KE, Semenza GL, Sharp FR. Induction of hypoxia-inducible factor-1 (HIF-1) and its target genes following focal ischaemia in rat brain. The European journal of neuroscience. 1999;11:4159–4170. doi: 10.1046/j.1460-9568.1999.00845.x. [DOI] [PubMed] [Google Scholar]
- 33.Kim JW, Tchernyshyov I, Semenza GL, Dang CV. HIF-1-mediated expression of pyruvate dehydrogenase kinase: a metabolic switch required for cellular adaptation to hypoxia. Cell metabolism. 2006;3:177–185. doi: 10.1016/j.cmet.2006.02.002. [DOI] [PubMed] [Google Scholar]
- 34.Clanton TL. Hypoxia-induced reactive oxygen species formation in skeletal muscle. J Appl Physiol (1985) 2007;102:2379–2388. doi: 10.1152/japplphysiol.01298.2006. [DOI] [PubMed] [Google Scholar]
- 35.Grune T, Merker K, Sandig G, Davies KJ. Selective degradation of oxidatively modified protein substrates by the proteasome. Biochemical and biophysical research communications. 2003;305:709–718. doi: 10.1016/S0006-291X(03)00809-X. [DOI] [PubMed] [Google Scholar]
- 36.Umanskaya A, et al. Genetically enhancing mitochondrial antioxidant activity improves muscle function in aging. Proceedings of the National Academy of Sciences of the United States of America. 2014;111:15250–15255. doi: 10.1073/pnas.1412754111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Kanski J, Hong SJ, Schoneich C. Proteomic analysis of protein nitration in aging skeletal muscle and identification of nitrotyrosine-containing sequences in vivo by nanoelectrospray ionization tandem mass spectrometry. The Journal of biological chemistry. 2005;280:24261–24266. doi: 10.1074/jbc.M501773200. [DOI] [PubMed] [Google Scholar]
- 38.Hoppeler H, Desplanches D. Muscle structural modifications in hypoxia. International journal of sports medicine. 1992;13(Suppl 1):S166–168. doi: 10.1055/s-2007-1024628. [DOI] [PubMed] [Google Scholar]
- 39.Hoppeler H, Howald H, Cerretelli P. Human muscle structure after exposure to extreme altitude. Experientia. 1990;46:1185–1187. doi: 10.1007/BF01936933. [DOI] [PubMed] [Google Scholar]
- 40.Powell CS, Jackson RM. Mitochondrial complex I, aconitase, and succinate dehydrogenase during hypoxia-reoxygenation: modulation of enzyme activities by MnSOD. American journal of physiology. Lung cellular and molecular physiology. 2003;285:L189–198. doi: 10.1152/ajplung.00253.2002. [DOI] [PubMed] [Google Scholar]
- 41.Cantu D, Schaack J, Patel M. Oxidative inactivation of mitochondrial aconitase results in iron and H2O2-mediated neurotoxicity in rat primary mesencephalic cultures. PloS one. 2009;4 doi: 10.1371/journal.pone.0007095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.West JB. J Appl Physiol (1985) 2007. Point: the lactate paradox does/does not occur during exercise at high altitude; pp. 2398–2399. [DOI] [PubMed] [Google Scholar]
- 43.Lundby C, Saltin B, van Hall G. The ‘lactate paradox’, evidence for a transient change in the course of acclimatization to severe hypoxia in lowlanders. Acta physiologica Scandinavica. 2000;170:265–269. doi: 10.1046/j.1365-201x.2000.00785.x. [DOI] [PubMed] [Google Scholar]
- 44.van Hall G, Calbet JA, Sondergaard H, Saltin B. The re-establishment of the normal blood lactate response to exercise in humans after prolonged acclimatization to altitude. The Journal of physiology. 2001;536:963–975. doi: 10.1111/j.1469-7793.2001.00963.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Xu H, Zheng X, Jia W, Yin S. Chromatography/Mass Spectrometry-Based Biomarkers in the Field of Obstructive Sleep Apnea. Medicine. 2015;94 doi: 10.1097/MD.0000000000001541. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Huss JM, Levy FH, Kelly DP. Hypoxia inhibits the peroxisome proliferator-activated receptor alpha/retinoid X receptor gene regulatory pathway in cardiac myocytes: a mechanism for O2-dependent modulation of mitochondrial fatty acid oxidation. The Journal of biological chemistry. 2001;276:27605–27612. doi: 10.1074/jbc.M100277200. [DOI] [PubMed] [Google Scholar]
- 47.Bostrom P, et al. Hypoxia converts human macrophages into triglyceride-loaded foam cells. Arteriosclerosis, thrombosis, and vascular biology. 2006;26:1871–1876. doi: 10.1161/01.ATV.0000229665.78997.0b. [DOI] [PubMed] [Google Scholar]
- 48.Rankin EB, et al. Hypoxia-inducible factor 2 regulates hepatic lipid metabolism. Molecular and cellular biology. 2009;29:4527–4538. doi: 10.1128/MCB.00200-09. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Oliveira GP, Dias CM, Pelosi P, Rocco PR. Understanding the mechanisms of glutamine action in critically ill patients. Anais da Academia Brasileira de Ciencias. 2010;82:417–430. doi: 10.1590/S0001-37652010000200018. [DOI] [PubMed] [Google Scholar]
- 50.DeBerardinis RJ, et al. Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis. Proceedings of the National Academy of Sciences of the United States of America. 2007;104:19345–19350. doi: 10.1073/pnas.0709747104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Metallo CM, et al. Reductive glutamine metabolism by IDH1 mediates lipogenesis under hypoxia. Nature. 2012;481:380–384. doi: 10.1038/nature10602. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Wise DR, et al. Hypoxia promotes isocitrate dehydrogenase-dependent carboxylation of alpha-ketoglutarate to citrate to support cell growth and viability. Proceedings of the National Academy of Sciences of the United States of America. 2011;108:19611–19616. doi: 10.1073/pnas.1117773108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Biolo G, Zorat F, Antonione R, Ciocchi B. Muscle glutamine depletion in the intensive care unit. The international journal of biochemistry & cell biology. 2005;37:2169–2179. doi: 10.1016/j.biocel.2005.05.001. [DOI] [PubMed] [Google Scholar]
- 54.Meador BM, Huey KA. Glutamine preserves skeletal muscle force during an inflammatory insult. Muscle & nerve. 2009;40:1000–1007. doi: 10.1002/mus.21430. [DOI] [PubMed] [Google Scholar]
- 55.Chamney C, Godar M, Garrigan E, Huey KA. Effects of glutamine supplementation on muscle function and stress responses in a mouse model of spinal cord injury. Experimental physiology. 2013;98:796–806. doi: 10.1113/expphysiol.2012.069658. [DOI] [PubMed] [Google Scholar]
- 56.Willam C, et al. HIF prolyl hydroxylases in the rat; organ distribution and changes in expression following hypoxia and coronary artery ligation. Journal of molecular and cellular cardiology. 2006;41:68–77. doi: 10.1016/j.yjmcc.2006.04.009. [DOI] [PubMed] [Google Scholar]
- 57.Connett RJ, Honig CR, Gayeski TE, Brooks GA. Defining hypoxia: a systems view of VO2, glycolysis, energetics, and intracellular PO2. J Appl Physiol (1985) 1990;68:833–842. doi: 10.1152/jappl.1990.68.3.833. [DOI] [PubMed] [Google Scholar]
- 58.Chandel NS, Budinger GR, Schumacker PT. Molecular oxygen modulates cytochrome c oxidase function. The Journal of biological chemistry. 1996;271:18672–18677. doi: 10.1074/jbc.271.31.18672. [DOI] [PubMed] [Google Scholar]
- 59.Milano G, Corno AF, Lippa S, Von Segesser LK, Samaja M. Chronic and intermittent hypoxia induce different degrees of myocardial tolerance to hypoxia-induced dysfunction. Exp Biol Med (Maywood) 2002;227:389–397. doi: 10.1177/153537020222700604. [DOI] [PubMed] [Google Scholar]
- 60.Spinazzi M, Casarin A, Pertegato V, Salviati L, Angelini C. Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells. Nature protocols. 2012;7:1235–1246. doi: 10.1038/nprot.2012.058. [DOI] [PubMed] [Google Scholar]
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