Mitochondrial Function and Reactive Oxygen/Nitrogen Species in Skeletal Muscle
Skeletal muscle fibers contain a large number of mitochondria, which produce ATP through oxidative phosphorylation (OXPHOS) and provide energy for muscle contraction. In this process, mitochondria also produce several types of “reactive species” as side product, such as reactive oxygen species and r...
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| Veröffentlicht in: | Frontiers in cell and developmental biology Jg. 10; S. 826981 |
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| Hauptverfasser: | , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
Switzerland
Frontiers Media SA
21.02.2022
Frontiers Media S.A |
| Schlagworte: | |
| ISSN: | 2296-634X, 2296-634X |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Skeletal muscle fibers contain a large number of mitochondria, which produce ATP through oxidative phosphorylation (OXPHOS) and provide energy for muscle contraction. In this process, mitochondria also produce several types of “reactive species” as side product, such as reactive oxygen species and reactive nitrogen species which have attracted interest. Mitochondria have been proven to have an essential role in the production of skeletal muscle reactive oxygen/nitrogen species (RONS). Traditionally, the elevation in RONS production is related to oxidative stress, leading to impaired skeletal muscle contractility and muscle atrophy. However, recent studies have shown that the optimal RONS level under the action of antioxidants is a critical physiological signal in skeletal muscle. Here, we will review the origin and physiological functions of RONS, mitochondrial structure and function, mitochondrial dynamics, and the coupling between RONS and mitochondrial oxidative stress. The crosstalk mechanism between mitochondrial function and RONS in skeletal muscle and its regulation of muscle stem cell fate and myogenesis will also be discussed. In all, this review aims to describe a comprehensive and systematic network for the interaction between skeletal muscle mitochondrial function and RONS. |
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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 Diego De Stefani, University of Padua, Italy These authors have contributed equally to this work Reviewed by: Pablo Hernansanz-Agustín, Spanish National Centre for Cardiovascular Research, Spain This article was submitted to Cellular Biochemistry, a section of the journal Frontiers in Cell and Developmental Biology Edited by: Luigi M. Terracciano, University of Basel, Switzerland |
| ISSN: | 2296-634X 2296-634X |
| DOI: | 10.3389/fcell.2022.826981 |