Department of Bioengineering, University of California, San Diego, California.
Department of Bioengineering, Bioinformatics & Systems Biology, University of California, San Diego, California.
Wiley Interdiscip Rev Syst Biol Med. 2020 Jan;12(1):e1462. doi: 10.1002/wsbm.1462. Epub 2019 Aug 13.
Decades of research in skeletal muscle physiology have provided multiscale insights into the structural and functional complexity of this important anatomical tissue, designed to accomplish the task of generating contraction, force and movement. Skeletal muscle can be viewed as a biomechanical device with various interacting components including the autonomic nerves for impulse transmission, vasculature for efficient oxygenation, and embedded regulatory and metabolic machinery for maintaining cellular homeostasis. The "omics" revolution has propelled a new era in muscle research, allowing us to discern minute details of molecular cross-talk required for effective coordination between the myriad interacting components for efficient muscle function. The objective of this review is to provide a systems-level, comprehensive mapping the molecular mechanisms underlying skeletal muscle structure and function, in health and disease. We begin this review with a focus on molecular mechanisms underlying muscle tissue development (myogenesis), with an emphasis on satellite cells and muscle regeneration. We next review the molecular structure and mechanisms underlying the many structural components of the muscle: neuromuscular junction, sarcomere, cytoskeleton, extracellular matrix, and vasculature surrounding muscle. We highlight aberrant molecular mechanisms and their possible clinical or pathophysiological relevance. We particularly emphasize the impact of environmental stressors (inflammation and oxidative stress) in contributing to muscle pathophysiology including atrophy, hypertrophy, and fibrosis. This article is categorized under: Physiology > Mammalian Physiology in Health and Disease Developmental Biology > Developmental Processes in Health and Disease Models of Systems Properties and Processes > Cellular Models.
几十年来,骨骼肌生理学的研究为理解这种重要解剖组织的结构和功能复杂性提供了多尺度的见解,其设计目的是完成产生收缩、力量和运动的任务。骨骼肌可以被视为一种具有各种相互作用组件的生物力学装置,包括用于冲动传递的自主神经、用于有效氧合的脉管系统,以及用于维持细胞内稳态的嵌入式调节和代谢机制。“组学”革命推动了肌肉研究的新纪元,使我们能够辨别出无数相互作用组件之间有效协调所需的分子相互作用的细微细节,以实现有效的肌肉功能。本综述的目的是提供一个系统水平的全面映射,以了解健康和疾病状态下骨骼肌结构和功能的分子机制。我们从肌肉组织发育(成肌)的分子机制开始综述,重点关注卫星细胞和肌肉再生。接下来,我们回顾了肌肉的许多结构成分的分子结构和机制:神经肌肉接头、肌节、细胞骨架、细胞外基质和肌肉周围的脉管系统。我们强调了异常的分子机制及其可能的临床或病理生理学相关性。我们特别强调环境应激源(炎症和氧化应激)对肌肉病理生理学的影响,包括萎缩、肥大和纤维化。本文归类于:生理学 > 哺乳动物生理学在健康和疾病中的应用 发育生物学 > 健康和疾病中的发育过程 系统属性和过程的模型 > 细胞模型。