TCA cycle rewiring fosters metabolic adaptation to oxygen restriction in skeletal muscle from rodents and humans
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 O 2 delivery by tuning its metabolism. The p...
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Published in | Scientific reports Vol. 7; no. 1; pp. 9723 - 16 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
29.08.2017
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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 O
2
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 O
2
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. |
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AbstractList | 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. 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 O 2 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 O 2 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. 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.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. 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 O 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 O 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. |
ArticleNumber | 9723 |
Author | Viganò, Agnese Capitanio, Daniele Grocott, Michael P. W. Levett, Denny Z. H. Samaja, Michele Cerretelli, Paolo Caretti, Anna Fania, Chiara Bravatà, Valentina Gelfi, Cecilia Torretta, Enrica Moriggi, Manuela |
Author_xml | – sequence: 1 givenname: Daniele orcidid: 0000-0001-7701-728X surname: Capitanio fullname: Capitanio, Daniele organization: Department of Biomedical Sciences for Health, University of Milan – sequence: 2 givenname: Chiara surname: Fania fullname: Fania, Chiara organization: UO Proteomica Clinica, IRCCS Policlinico San Donato – sequence: 3 givenname: Enrica surname: Torretta fullname: Torretta, Enrica organization: Department of Biomedical Sciences for Health, University of Milan – sequence: 4 givenname: Agnese surname: Viganò fullname: Viganò, Agnese organization: Department of Biomedical Sciences for Health, University of Milan – sequence: 5 givenname: Manuela surname: Moriggi fullname: Moriggi, Manuela organization: CNR-Institute of Bioimaging and Molecular Physiology – sequence: 6 givenname: Valentina surname: Bravatà fullname: Bravatà, Valentina organization: CNR-Institute of Bioimaging and Molecular Physiology – sequence: 7 givenname: Anna orcidid: 0000-0001-6140-6969 surname: Caretti fullname: Caretti, Anna organization: Department of Health Sciences, University of Milan – sequence: 8 givenname: Denny Z. H. surname: Levett fullname: Levett, Denny Z. H. organization: Centre for Altitude, Space, and Extreme Environment Medicine, University College London (UCL), Institute of Child Health, University College London, Anaesthesia and Critical Care Research Unit, University Hospital Southampton, NHS Foundation Trust, Integrative Physiology and Critical Illness Group, Division of Clinical and Experimental Science, Faculty of Medicine, University of Southampton – sequence: 9 givenname: Michael P. W. surname: Grocott fullname: Grocott, Michael P. W. organization: Centre for Altitude, Space, and Extreme Environment Medicine, University College London (UCL), Institute of Child Health, University College London, Anaesthesia and Critical Care Research Unit, University Hospital Southampton, NHS Foundation Trust, Integrative Physiology and Critical Illness Group, Division of Clinical and Experimental Science, Faculty of Medicine, University of Southampton – sequence: 10 givenname: Michele surname: Samaja fullname: Samaja, Michele organization: Department of Health Sciences, University of Milan – sequence: 11 givenname: Paolo surname: Cerretelli fullname: Cerretelli, Paolo organization: CNR-Institute of Bioimaging and Molecular Physiology – sequence: 12 givenname: Cecilia orcidid: 0000-0002-2996-6912 surname: Gelfi fullname: Gelfi, Cecilia email: cecilia.gelfi@unimi.it organization: Department of Biomedical Sciences for Health, University of Milan, UO Proteomica Clinica, IRCCS Policlinico San Donato, CNR-Institute of Bioimaging and Molecular Physiology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28852047$$D View this record in MEDLINE/PubMed |
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SubjectTerms | 38 38/77 631/45/475/2290 692/4017 82 82/1 82/29 82/58 Adaptation, Physiological Animals Autophagy Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Citric Acid Cycle Energy demand Energy Metabolism Enzymatic activity Gene Expression Glutamine Hexosamines - metabolism High-altitude environments Homeostasis Human subjects Humanities and Social Sciences Humans Hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - genetics Hypoxia-Inducible Factor 1, alpha Subunit - metabolism Metabolic Networks and Pathways Metabolism Models, Biological multidisciplinary Muscle, Skeletal - metabolism Musculoskeletal system Oxygen - metabolism Proteome Proteomics Proteomics - methods Rodentia Rodents Science Science (multidisciplinary) Signal Transduction Skeletal muscle Time Factors Tricarboxylic acid cycle |
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Title | TCA cycle rewiring fosters metabolic adaptation to oxygen restriction in skeletal muscle from rodents and humans |
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