Loss of Myostatin Alters Mitochondrial Oxidative Phosphorylation, TCA Cycle Activity, and ATP Production in Skeletal Muscle

• Published in: International journal of molecular sciences 2022-12, Vol.23 (24), p.15707
• Main Authors: Wang, Xueqiao, Wei, Zhuying, Gu, Mingjuan, Zhu, Lin, Hai, Chao, Di, Anqi, Wu, Di, Bai, Chunling, Su, Guanghua, Liu, Xuefei, Yang, Lei, Li, Guangpeng
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Animals; Body temperature; Calorimetry; CRISPR; Dehydrogenases; Electron transport; Energy; Energy balance; Energy metabolism; Enzyme-linked immunosorbent assay; Enzymes; Gene expression; Glucose metabolism; Homeostasis; Hypertrophy; Investigations; Kinases; Lipolysis; Metabolic rate; Metabolism; Metabolites; Mice; Mice, Knockout; Mitochondria; Mitochondria - metabolism; Muscle, Skeletal - metabolism; Muscles; Musculoskeletal system; Mutation; Myostatin; Myostatin - genetics; Myostatin - metabolism; Oxidative metabolism; Oxidative Phosphorylation; Phenotypes; Phosphorylation; Proteins; Respiration; Skeletal muscle; Smad2 protein; Tricarboxylic acid cycle
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232415707

Myostatin (MSTN) is an important negative regulator of skeletal muscle growth in animals. A lack of MSTN promotes lipolysis and glucose metabolism but inhibits oxidative phosphorylation (OXPHOS). Here, we aimed to investigate the possible mechanism of MSTN regulating the mitochondrial energy homeostasis of skeletal muscle. To this end, MSTN knockout mice were generated by the CRISPR/Cas9 technique. Expectedly, the MSTN null ( ) mouse has a hypermuscular phenotype. The muscle metabolism of the mice was detected by an enzyme-linked immunosorbent assay, indirect calorimetry, ChIP-qPCR, and RT-qPCR. The resting metabolic rate and body temperature of the mice were significantly reduced. The loss of MSTN not only significantly inhibited the production of ATP by OXPHOS and decreased the activity of respiratory chain complexes, but also inhibited key rate-limiting enzymes related to the TCA cycle and significantly reduced the ratio of NADH/NAD+ in the mice, which then greatly reduced the total amount of ATP. Further ChIP-qPCR results confirmed that the lack of MSTN inhibited both the TCA cycle and OXPHOS, resulting in decreased ATP production. The reason may be that Smad2/3 is not sufficiently bound to the promoter region of the rate-limiting enzymes Idh2 and Idh3a of the TCA cycle, thus affecting their transcription.