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细胞外基质金属蛋白酶诱导因子(EMMPRIN/CD147)作为一种新的肌细胞分化调节因子。

Extracellular matrix metalloproteinase inducer (EMMPRIN/CD147) as a novel regulator of myogenic cell differentiation.

机构信息

Laboratoire CRRET, CNRS EAC 7149, Université Paris-Est Créteil, Créteil, France.

出版信息

J Cell Physiol. 2011 Jan;226(1):141-9. doi: 10.1002/jcp.22315.

Abstract

Matrix metalloproteinases (MMPs) are thought to play an important role in skeletal muscle cell growth and differentiation. In view of the MMP inducing function of EMMPRIN/CD147, its role in myogenic cell differentiation was investigated. EMMPRIN level increased during differentiation of both rat primary myoblasts derived from satellite cells and mouse C2.7 myogenic cells and was associated with an alteration in its molecular forms. In parallel, expression of pro-MMP-9 gradually decreased and that of pro-MMP-2 and active MMP-2 increased. While small interfering RNA (siRNA) inhibition of EMMPRIN expression accelerated cell differentiation, exogenously added recombinant EMMPRIN inhibited differentiation by an MMP-mediated mechanism, as the MMP inhibitor marimastat abrogated EMMPRIN's effect. Our results further suggest that EMMPRIN regulates differentiation through an MMP activation of transforming growth factor beta (TGFβ), a known inhibitor of myoblast's differentiation, as the increased activation and signaling of TGFβ by EMMPRIN was attenuated in the presence of marimastat. EMMPRIN inhibition may thus represent a novel strategy in the treatment of muscular degenerative disorders.

摘要

基质金属蛋白酶(MMPs)被认为在骨骼肌细胞的生长和分化中发挥重要作用。鉴于 EMMPRIN/CD147 具有诱导 MMP 的功能,研究了其在成肌细胞分化中的作用。大鼠卫星细胞来源的原代肌母细胞和小鼠 C2.7 成肌细胞分化过程中 EMMPRIN 水平增加,并且其分子形式发生改变。同时,前 MMP-9 的表达逐渐减少,而前 MMP-2 和活性 MMP-2 的表达增加。虽然小干扰 RNA(siRNA)抑制 EMMPRIN 表达可加速细胞分化,但外源性添加重组 EMMPRIN 通过 MMP 介导的机制抑制分化,因为 MMP 抑制剂 marimastat 消除了 EMMPRIN 的作用。我们的结果进一步表明,EMMPRIN 通过 MMP 激活转化生长因子β(TGFβ)来调节分化,TGFβ 是已知的成肌细胞分化抑制剂,因为 marimastat 存在时,EMMPRIN 增加 TGFβ 的激活和信号转导被减弱。因此,EMMPRIN 抑制可能成为治疗肌肉退行性疾病的一种新策略。

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