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

Abstract

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.

• Authors: Mingwei Guo, Liping Xiang, Jing Yao, Jun Zhang, Shuangshuang Zhu, Dongmei Wang, Caizhi Liu, Guoqiang Li, Jiawen Wang, Yuqing Gao, Cen Xie, Xinran Ma, Lingyan Xu, Jian Zhou
• Journal: Frontiers in endocrinology (Front Endocrinol (Lausanne)) Vol. 13 Pg. 851520 ( 2022) ISSN: 1664-2392 [Print] Switzerland
• PMID: 35265044 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2022 Guo, Xiang, Yao, Zhang, Zhu, Wang, Liu, Li, Wang, Gao, Xie, Ma, Xu and Zhou.

Topics

• Animals
• Gene Expression Profiling
• Inflammation (pathology)
• Liver Cirrhosis
• Mice
• Muscle, Skeletal (metabolism)
• Non-alcoholic Fatty Liver Disease (genetics, metabolism)