Hu Li-Yen R, Ackermann Maegen A, Kontrogianni-Konstantopoulos Aikaterini
Department of Biochemistry and Molecular Biology, School of Medicine, University of Maryland, 108 N Greene Street, Baltimore, MD 21201, USA.
Biomed Res Int. 2015;2015:714197. doi: 10.1155/2015/714197. Epub 2015 Apr 15.
The sarcomeric M-region anchors thick filaments and withstands the mechanical stress of contractions by deformation, thus enabling distribution of physiological forces along the length of thick filaments. While the role of the M-region in supporting myofibrillar structure and contractility is well established, its role in mediating additional cellular processes has only recently started to emerge. As such, M-region is the hub of key protein players contributing to cytoskeletal remodeling, signal transduction, mechanosensing, metabolism, and proteasomal degradation. Mutations in genes encoding M-region related proteins lead to development of severe and lethal cardiac and skeletal myopathies affecting mankind. Herein, we describe the main cellular processes taking place at the M-region, other than thick filament assembly, and discuss human myopathies associated with mutant or truncated M-region proteins.
肌节M区锚定粗肌丝,并通过变形承受收缩的机械应力,从而使生理力沿粗肌丝长度分布。虽然M区在支持肌原纤维结构和收缩性方面的作用已得到充分证实,但其在介导其他细胞过程中的作用直到最近才开始显现。因此,M区是关键蛋白质发挥作用的中心,这些蛋白质参与细胞骨架重塑、信号转导、机械传感、代谢和蛋白酶体降解。编码与M区相关蛋白质的基因突变会导致影响人类的严重致命性心脏和骨骼肌病。在此,我们描述了除粗肌丝组装外,在M区发生的主要细胞过程,并讨论了与突变或截短的M区蛋白相关的人类肌病。