Grounds Miranda D
School of Anatomy, Physiology and Human Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Perth 6009, WA, Australia.
Int J Biochem Cell Biol. 2014 Nov;56:56-65. doi: 10.1016/j.biocel.2014.09.010. Epub 2014 Sep 19.
A more precise definition of the term 'skeletal muscle regeneration' is required to reduce confusion and misconceptions. In this paper the term is used only for events that follow myofibre necrosis, to result in myogenesis and new muscle formation: other key events include early inflammation and revascularisation, and later fibrosis and re-innervation. The term 'muscle regeneration' is sometimes used casually for situations that do not involve myonecrosis; such as restoration of muscle mass by hypertrophy after atrophy, and other forms of damage to muscle tissue components. These situations are excluded from the definition in this paper which is focussed on mammalian muscles with the long-term aim of clinical translation to enhance new muscle formation after acute or chronic injury or during surgery to replace whole muscles. The paper briefly outlines the cellular events involved in myogenesis during development and post-natal muscle growth, discusses the role of satellite cells in mature normal muscles, and the likely incidence of myofibre necrosis/regeneration in healthy ageing mammals (even when subjected to exercise). The importance of the various components of regeneration is outlined to emphasise that problems in each of these aspects can influence overall new muscle formation; thus care is needed for correct interpretation of altered kinetics. Various markers used to identify regenerating myofibres are critically discussed and, since these can all occur in other conditions, caution is required for accurate interpretation of these cellular events. Finally, clinical situations are outlined where there is a need to enhance skeletal muscle regeneration: these include acute and chronic injuries or transplantation with bioengineering to form new muscles, therapeutic approaches to muscular dystrophies, and comment on proposed stem cell therapies to reduce age-related loss of muscle mass and function. This article is part of a directed issue entitled: Regenerative Medicine: the challenge of translation.
需要对“骨骼肌再生”一词给出更精确的定义,以减少混淆和误解。在本文中,该术语仅用于指在肌纤维坏死后发生的、导致肌生成和新肌肉形成的事件:其他关键事件包括早期炎症和血管再生,以及后期的纤维化和重新神经支配。“肌肉再生”一词有时被随意用于不涉及肌坏死的情况;例如萎缩后通过肥大恢复肌肉质量,以及肌肉组织成分的其他形式损伤。本文的定义不包括这些情况,本文聚焦于哺乳动物肌肉,其长期目标是进行临床转化,以增强急性或慢性损伤后或手术替换整块肌肉时的新肌肉形成。本文简要概述了发育过程中和出生后肌肉生长期间肌生成所涉及的细胞事件,讨论了卫星细胞在成熟正常肌肉中的作用,以及健康衰老哺乳动物(即使进行运动)中肌纤维坏死/再生的可能发生率。概述了再生各个组成部分的重要性,以强调这些方面中的每一个出现问题都可能影响整体新肌肉形成;因此,需要谨慎正确解释动力学变化。对用于识别再生肌纤维的各种标志物进行了批判性讨论,并且由于这些标志物都可能出现在其他情况中,因此需要谨慎准确解释这些细胞事件。最后,概述了需要增强骨骼肌再生的临床情况:这些情况包括急性和慢性损伤或通过生物工程移植形成新肌肉、治疗肌肉萎缩症的方法,以及对提议的干细胞疗法的评论,以减少与年龄相关的肌肉质量和功能丧失。本文是名为《再生医学:转化的挑战》的定向专题文章的一部分。