Skeletal muscle: molecular structure, myogenesis, biological functions, and diseases

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL MedComm Pub Date : 2024-07-10 DOI:10.1002/mco2.649
Lan-Ting Feng, Zhi-Nan Chen, Huijie Bian
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Abstract

Skeletal muscle is an important motor organ with multinucleated myofibers as its smallest cellular units. Myofibers are formed after undergoing cell differentiation, cell–cell fusion, myonuclei migration, and myofibril crosslinking among other processes and undergo morphological and functional changes or lesions after being stimulated by internal or external factors. The above processes are collectively referred to as myogenesis. After myofibers mature, the function and behavior of skeletal muscle are closely related to the voluntary movement of the body. In this review, we systematically and comprehensively discuss the physiological and pathological processes associated with skeletal muscles from five perspectives: molecule basis, myogenesis, biological function, adaptive changes, and myopathy. In the molecular structure and myogenesis sections, we gave a brief overview, focusing on skeletal muscle-specific fusogens and nuclei-related behaviors including cell–cell fusion and myonuclei localization. Subsequently, we discussed the three biological functions of skeletal muscle (muscle contraction, thermogenesis, and myokines secretion) and its response to stimulation (atrophy, hypertrophy, and regeneration), and finally settled on myopathy. In general, the integration of these contents provides a holistic perspective, which helps to further elucidate the structure, characteristics, and functions of skeletal muscle.

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骨骼肌:分子结构、肌肉生成、生物功能和疾病。
骨骼肌是一种重要的运动器官,其最小的细胞单位是多核肌纤维。肌纤维的形成要经过细胞分化、细胞-细胞融合、肌核迁移和肌原纤维交联等过程,并在内部或外部因素的刺激下发生形态和功能的变化或病变。上述过程统称为肌生成。肌纤维成熟后,骨骼肌的功能和行为与人体的自主运动密切相关。在这篇综述中,我们将从分子基础、肌生成、生物功能、适应性变化和肌病五个方面系统全面地讨论与骨骼肌相关的生理和病理过程。在分子结构和肌生成部分,我们简要概述了骨骼肌特异性致裂原和细胞核相关行为,包括细胞-细胞融合和肌核定位。随后,我们讨论了骨骼肌的三种生物功能(肌肉收缩、产热和肌动蛋白分泌)及其对刺激的反应(萎缩、肥大和再生),最后讨论了肌病。总的来说,这些内容的整合提供了一个整体视角,有助于进一步阐明骨骼肌的结构、特征和功能。
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CiteScore
6.70
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0.00%
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审稿时长
10 weeks
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