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骨形态发生蛋白 4 通过磷脂酰肌醇 3 激酶介导的 N-钙黏蛋白上调,刺激神经球附着和神经球中的神经干细胞星形胶质发生。

Bone morphogenetic protein 4 stimulates attachment of neurospheres and astrogenesis of neural stem cells in neurospheres via phosphatidylinositol 3 kinase-mediated upregulation of N-cadherin.

机构信息

Translational Research Center for Protein Function Control, College of Life Science and Biotechnology, Yonsei University, Seoul 120-749, Korea.

出版信息

Neuroscience. 2010 Sep 29;170(1):8-15. doi: 10.1016/j.neuroscience.2010.07.020. Epub 2010 Jul 16.

DOI:10.1016/j.neuroscience.2010.07.020
PMID:20638445
Abstract

The neurosphere culture system is useful for expanding neural stem cells (NSCs) without affecting self-renewal potential and multipotency. However, the extrinsic signals that affect the formation or dissociation of neurospheres are poorly understood. Here, we found that bone morphogenetic protein 4 (BMP4) induced the attachment of neurospheres, astrocytic differentiation, and migration of neurosphere NSCs. These outcomes were accompanied by Akt activation and upregulation of the adhesion molecule, N-cadherin. A phosphatidylinositol 3 kinase (PI3 kinase) inhibitor (LY294002) blocked attachment of neurosphere, astrocytic differentiation, migration, and N-cadherin upregulation of neurosphre NSCs. The PI3 kinase-Akt pathway appeared to selectively mediate the effects of BMP4, as neurosphere attachment was unaffected by MEK inhibitors (PD98059 and U0126). Importantly, a neutralizing N-cadherin antibody inhibited BMP4-induced neurosphere attachment, astrocytic differentiation, and migration of neurosphere NSCs. Together, these findings show that BMP4-induced attachment of neurospheres is related to the astrocytic differentiation of these cells and that these effects are attributable, at least in part, to PI3 kinase-Akt pathway-dependent induction of N-cadherin.

摘要

神经球培养系统可用于扩增神经干细胞(NSCs),而不影响其自我更新能力和多能性。然而,影响神经球形成或解离的外在信号仍知之甚少。在这里,我们发现骨形态发生蛋白 4(BMP4)可诱导神经球黏附、星形胶质细胞分化和神经球 NSCs 迁移。这些结果伴随着 Akt 的激活和黏附分子 N-钙黏蛋白的上调。PI3 激酶(PI3K)抑制剂(LY294002)阻断了神经球黏附、星形胶质细胞分化、迁移和 N-钙黏蛋白上调的神经球 NSCs。PI3K-Akt 通路似乎选择性地介导了 BMP4 的作用,因为 MEK 抑制剂(PD98059 和 U0126)对神经球黏附没有影响。重要的是,中和 N-钙黏蛋白抗体抑制了 BMP4 诱导的神经球黏附、星形胶质细胞分化和神经球 NSCs 的迁移。总之,这些发现表明 BMP4 诱导的神经球黏附与这些细胞的星形胶质细胞分化有关,这些作用至少部分归因于 PI3K-Akt 通路依赖性诱导 N-钙黏蛋白。

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