4.7 Article

Comprehensive Transcriptome Profiling of NAFLD- and NASH-Induced Skeletal Muscle Dysfunction

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2022.851520

Keywords

NAFLD; NASH; quadriceps muscle; lipid deposition; insulin resistance; myokines

Funding

  1. National Key Research and Development Program of China [2019YFA0904500]
  2. Science and Technology Commission of Shanghai Municipality [21140904300]
  3. National Natural Science Foundation of China [32022034, 31770840, 32071148, 31800989]
  4. Fundamental Research Funds for the Central Universities
  5. ECNU public platform for Innovation [011]
  6. instruments sharing platform of School of Life Sciences

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This study provides a comprehensive analysis of the molecular characteristics of skeletal muscles in NAFLD and NASH mouse models. The analysis reveals that NAFLD and NASH impair glucose and lipid metabolism and deteriorate functionality in skeletal muscle. Additionally, myokines are identified as potential mediators of the crosstalk between muscles and other metabolic organs in pathological conditions.
Nonalcoholic fatty liver disease (NAFLD), characterized by extensive triglyceride accumulation in hepatocytes, may progress to nonalcoholic steatohepatitis (NASH) with liver fibrosis and inflammation and increase the risk of cirrhosis, cancer, and death. It has been reported that physical exercise is effective in ameliorating NAFLD and NASH, while skeletal muscle dysfunctions, including lipid deposition and weakness, are accompanied with NAFLD and NASH. However, the molecular characteristics and alterations in skeletal muscle in the progress of NAFLD and NASH remain unclear. In the present study, we provide a comprehensive analysis on the similarity and heterogeneity of quadriceps muscle in NAFLD and NASH mice models by RNA sequencing. Importantly, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway functional enrichment analysis revealed that NAFLD and NASH led to impaired glucose and lipid metabolism and deteriorated functionality in skeletal muscle. Besides this, we identified that myokines possibly mediate the crosstalk between muscles and other metabolic organs in pathological conditions. Overall, our analysis revealed a comprehensive understanding of the molecular signature of skeletal muscles in NAFLD and NASH, thus providing a basis for physical exercise as an intervention against liver diseases.

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