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成肌细胞融合:一“合”不易。

Myoblast fusion: when it takes more to make one.

机构信息

Program in Developmental Biology, Sloan-Kettering Institute, New York, NY 10065, USA.

出版信息

Dev Biol. 2010 May 1;341(1):66-83. doi: 10.1016/j.ydbio.2009.10.024. Epub 2009 Nov 20.

Abstract

Cell-cell fusion is a crucial and highly regulated event in the genesis of both form and function of many tissues. One particular type of cell fusion, myoblast fusion, is a key cellular process that shapes the formation and repair of muscle. Despite its importance for human health, the mechanisms underlying this process are still not well understood. The purpose of this review is to highlight the recent literature pertaining to myoblast fusion and to focus on a comparison of these studies across several model systems, particularly the fly, zebrafish and mouse. Advances in technical analysis and imaging have allowed identification of new fusion genes and propelled further characterization of previously identified genes in each of these systems. Among the cellular steps identified as critical for myoblast fusion are migration, recognition, adhesion, membrane alignment and membrane pore formation and resolution. Importantly, striking new evidence indicates that orthologous genes govern several of these steps across these species. Taken together, comparisons across three model systems are illuminating a once elusive process, providing exciting new insights and a useful framework of genes and mechanisms.

摘要

细胞融合是许多组织形态和功能形成过程中的一个关键且高度调控的事件。肌母细胞融合是一种特殊的细胞融合类型,是塑造肌肉形成和修复的关键细胞过程。尽管它对人类健康很重要,但这个过程的机制仍未被很好地理解。本文的目的是强调最近关于肌母细胞融合的文献,并特别关注这些研究在几个模型系统中的比较,特别是在果蝇、斑马鱼和小鼠中。技术分析和成像的进步使新的融合基因得以识别,并推动了对每个系统中以前鉴定的基因的进一步表征。在被确定为肌母细胞融合关键的细胞步骤中,有迁移、识别、黏附、膜对齐、膜孔形成和修复。重要的是,引人注目的新证据表明,在这些物种中,同源基因控制着其中的几个步骤。总之,这三个模型系统的比较为这一曾经难以捉摸的过程提供了启示,为基因和机制提供了令人兴奋的新见解和有用的框架。

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The small G-proteins Rac1 and Cdc42 are essential for myoblast fusion in the mouse.小G蛋白Rac1和Cdc42对小鼠成肌细胞融合至关重要。
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