使用SILAC和Shotgun蛋白质组学分析骨骼肌发生的分泌组学。

International journal of proteomics Pub Date : 2011-01-01 Epub Date: 2011-03-29 DOI:10.1155/2011/329467
C Y X'avia Chan, John C McDermott, K W Michael Siu
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引用次数: 15

摘要

骨骼肌的形成是一个多步骤的过程,从成肌细胞增殖开始,然后是细胞周期停滞,最后通过单核成肌细胞融合形成多核肌管。每个步骤都是由充分记录的细胞内因子精心安排的,例如细胞质信号分子和核转录因子。无论如何,更全面地了解肌生成调控的关键一步是探索能够激发下游细胞内因子的细胞外因子。这可以进一步为维持正常肌肉发育的外部信号的急性细胞反应提供有价值的见解。在本文中,我们研究了响应细胞外信号的细胞内因子,这些细胞外信号负责肌发生过程中的级联事件:成肌细胞增殖、成肌细胞的细胞周期阻滞和成肌细胞向肌管的分化。这种对肌肉发育的细胞外视角的关注说明了我们基于质谱的蛋白质组学方法来识别骨骼肌发生过程中差异表达的分泌因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Secretome Analysis of Skeletal Myogenesis Using SILAC and Shotgun Proteomics.

Myogenesis, the formation of skeletal muscle, is a multistep event that commences with myoblast proliferation, followed by cell-cycle arrest, and finally the formation of multinucleated myotubes via fusion of mononucleated myoblasts. Each step is orchestrated by well-documented intracellular factors, such as cytoplasmic signalling molecules and nuclear transcription factors. Regardless, the key step in getting a more comprehensive understanding of the regulation of myogenesis is to explore the extracellular factors that are capable of eliciting the downstream intracellular factors. This could further provide valuable insight into the acute cellular response to extrinsic cues in maintaining normal muscle development. In this paper, we survey the intracellular factors that respond to extracellular cues that are responsible for the cascades of events during myogenesis: myoblast proliferation, cell-cycle arrest of myoblasts, and differentiation of myoblasts into myotubes. This focus on extracellular perspective of muscle development illustrates our mass spectrometry-based proteomic approaches to identify differentially expressed secreted factors during skeletal myogenesis.

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