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体重指数增加的人类骨骼肌中合胞素-1表达增加。

Increased Expression of Syncytin-1 in Skeletal Muscle of Humans With Increased Body Mass Index.

作者信息

Ravichandran Jayachandran, Roust Lori R, Katsanos Christos S

机构信息

School of Life Sciences, Arizona State University, Tempe, AZ, United States.

College of Medicine, Mayo Clinic in Arizona, Scottsdale, AZ, United States.

出版信息

Front Physiol. 2022 Apr 4;13:858341. doi: 10.3389/fphys.2022.858341. eCollection 2022.

DOI:10.3389/fphys.2022.858341
PMID:35444566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9013906/
Abstract

Obesity negatively impacts skeletal muscle protein metabolism, and also impairs skeletal muscle maintenance and regeneration. We analyzed muscle biopsy samples from humans with increased body mass index (BMI) (i.e. > 30 kg/m) and controls (i.e., BMI < 25 kg/m) for expression of syncytin-1, a fusogenic protein regulating skeletal muscle regeneration. When compared to controls, humans with increased BMI and concomitant reduction in muscle protein synthesis had higher expression of syncytin-1 in skeletal muscle ( < 0.05). Across human subjects, muscle protein synthesis correlated inversely ( = -0.51; = 0.03) with syncytin-1 expression in muscle. Using a C2C12 cell line we found that expression of syncytin-A (i.e, corresponding protein in murine tissue) is increased by insulin, and that this response is impaired in the presence of fatty acids, whose metabolism is altered within the metabolic environment induced by increased BMI. In C2C12 cells, the response of the protein 4E-BP1, which signals increase in protein synthesis in muscle, resembled that of syncytin-A. These findings provide novel insights into the expression of syncytin-1 in skeletal muscle of humans with increased BMI, as well as its basic regulation by insulin and fatty acids in muscle. The findings signify the need for further research into the regulation of syncytin-1 in skeletal muscle of humans with increased BMI, as well as its biological implications for altering muscle protein metabolism and regeneration.

摘要

肥胖对骨骼肌蛋白质代谢产生负面影响,还会损害骨骼肌的维持和再生。我们分析了体重指数(BMI)升高(即>30kg/m²)的人和对照组(即BMI<25kg/m²)的肌肉活检样本,以检测合胞素-1的表达,合胞素-1是一种调节骨骼肌再生的融合蛋白。与对照组相比,BMI升高且肌肉蛋白质合成减少的人骨骼肌中合胞素-1的表达更高(P<0.05)。在所有人类受试者中,肌肉蛋白质合成与肌肉中合胞素-1的表达呈负相关(r=-0.51;P=0.03)。我们使用C2C12细胞系发现,胰岛素可增加合胞素-A(即小鼠组织中的相应蛋白)的表达,并且在脂肪酸存在的情况下这种反应会受损,在BMI升高所诱导的代谢环境中脂肪酸的代谢会发生改变。在C2C12细胞中,蛋白质4E-BP1(其信号表明肌肉中蛋白质合成增加)的反应与合胞素-A相似。这些发现为BMI升高的人类骨骼肌中合胞素-1的表达及其在肌肉中受胰岛素和脂肪酸的基本调节提供了新的见解。这些发现表明需要进一步研究BMI升高的人类骨骼肌中合胞素-1的调节,以及其对改变肌肉蛋白质代谢和再生的生物学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/5ad10c01b462/fphys-13-858341-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/ec21922cd5d7/fphys-13-858341-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/60d297f13cb1/fphys-13-858341-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/5ad10c01b462/fphys-13-858341-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/ec21922cd5d7/fphys-13-858341-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/60d297f13cb1/fphys-13-858341-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb5b/9013906/5ad10c01b462/fphys-13-858341-g003.jpg

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本文引用的文献

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