Suppr超能文献

小分子诱导骨髓间充质干细胞向神经样细胞分化。

Small molecule induction of neural-like cells from bone marrow-mesenchymal stem cells.

机构信息

Department of Neurology, Second Affiliated Hospital of Nanchang University, Nanchang City, China.

出版信息

J Cell Biochem. 2012 May;113(5):1527-36. doi: 10.1002/jcb.24021.

Abstract

Bone marrow-derived mesenchymal stem cells (MSCs) have been demonstrated to be able to differentiate into neuron-like cell, but the precise mechanisms controlling this process are unclear. We report here that LY294002, a small molecule inhibitor of PI3K/AKT signal pathway, can inhibit proliferation and promote neuronal differentiation of MSCs after MSCs incubated with LY294002 for 6 and 12 h. RT-PCR results indicated that mRNA expression of α5β1 integrin significantly increased in neuron-like cell from MSCs. Interestingly, neuron-like cells derived by this method adhere much more strongly than MSCs, which was related to the expression of α5β1 integrin and FAK phosphorylation. However, these effects could be attenuated by LiCL or GSK-3β-siRNA. Our results indicate that activation GSK-3β signaling may be involved in MSCs proliferation, differentiation, and adhesion. Furthermore, this study demonstrates that small molecule regulators of PI3K/AKT signaling may be valuable tools for stem cell research aimed at treatment of neurodegenerative disease.

摘要

骨髓间充质干细胞(MSCs)已被证明能够分化为神经元样细胞,但控制这一过程的确切机制尚不清楚。我们在这里报告,LY294002,一种 PI3K/AKT 信号通路的小分子抑制剂,在 MSCs 孵育 6 和 12 小时后,可以抑制增殖并促进 MSCs 的神经元分化。RT-PCR 结果表明,α5β1 整合素的 mRNA 表达在神经元样细胞中显著增加。有趣的是,通过这种方法诱导的神经元样细胞比 MSCs 更牢固地附着,这与α5β1 整合素和 FAK 磷酸化的表达有关。然而,这些效应可以被 LiCL 或 GSK-3β-siRNA 减弱。我们的结果表明,激活 GSK-3β 信号可能参与 MSCs 的增殖、分化和黏附。此外,这项研究表明,PI3K/AKT 信号的小分子调节剂可能是针对神经退行性疾病治疗的干细胞研究的有价值的工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验