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胰岛素样生长因子结合蛋白5通过与胰岛素样生长因子-II结合并开启胰岛素样生长因子-II的自动调节环来调节肌肉细胞分化。

IGFBP-5 regulates muscle cell differentiation by binding to IGF-II and switching on the IGF-II auto-regulation loop.

作者信息

Ren Hongxia, Yin Ping, Duan Cunming

机构信息

Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

J Cell Biol. 2008 Sep 8;182(5):979-91. doi: 10.1083/jcb.200712110. Epub 2008 Sep 1.

Abstract

IGF-II stimulates both mitogenesis and myogenesis through its binding and activation of the IGF-I receptor (IGF-IR). How this growth factor pathway promotes these two opposite cellular responses is not well understood. We investigate whether local IGF binding protein-5 (IGFBP-5) promotes the myogenic action of IGF-II. IGFBP-5 is induced before the elevation of IGF-II expression during myogenesis. Knockdown of IGFBP-5 impairs myogenesis and suppresses IGF-II gene expression. IGF-II up-regulates its own gene expression via the PI3K-Akt signaling pathway. Adding IGF-II or constitutively activating Akt rescues the IGFBP-5 knockdown-caused defects. However, an IGF analogue that binds to the IGF-IR but not IGFBP has only a limited effect. When added with low concentrations of IGF-II, IGFBP-5 restores IGF-II expression and myogenic differentiation, whereas an IGF binding-deficient IGFBP-5 mutant has no effect. These findings suggest that IGFBP-5 promotes muscle cell differentiation by binding to and switching on the IGF-II auto-regulation loop.

摘要

胰岛素样生长因子-II(IGF-II)通过与胰岛素样生长因子-I受体(IGF-IR)结合并激活该受体,刺激有丝分裂和肌生成。目前对于这条生长因子信号通路如何促进这两种相反的细胞反应还了解得不够透彻。我们研究了局部胰岛素样生长因子结合蛋白-5(IGFBP-5)是否促进IGF-II的肌生成作用。在肌生成过程中,IGFBP-5在IGF-II表达升高之前就被诱导产生。敲低IGFBP-5会损害肌生成并抑制IGF-II基因表达。IGF-II通过PI3K-Akt信号通路上调其自身的基因表达。添加IGF-II或组成型激活Akt可挽救由IGFBP-5敲低导致的缺陷。然而,一种与IGF-IR结合但不与IGFBP结合的IGF类似物只有有限的作用。当与低浓度的IGF-II一起添加时,IGFBP-5可恢复IGF-II表达和肌生成分化,而一种缺乏IGF结合能力的IGFBP-5突变体则没有作用。这些发现表明,IGFBP-5通过结合并开启IGF-II的自调节环路来促进肌肉细胞分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64c8/2528583/a900b363b003/jcb1820979f01.jpg

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