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首页> 外文期刊>Journal of Neuroscience Research >Brain-derived neurotrophic factor stimulates the neural differentiation of human umbilical cord blood-derived mesenchymal stem cells and survival of differentiated cells through MAPK/ERK and PI3K/Akt-dependent signaling pathways.
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Brain-derived neurotrophic factor stimulates the neural differentiation of human umbilical cord blood-derived mesenchymal stem cells and survival of differentiated cells through MAPK/ERK and PI3K/Akt-dependent signaling pathways.

机译:脑源性神经营养因子通过MAPK / ERK和PI3K / Akt依赖性信号通路刺激人脐带血间充质干细胞的神经分化和分化细胞的存活。

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摘要

Brain-derived neurotrophic factor (BDNF) plays an important role in the differentiation, development, and survival of neural stem cells. In this study, we analyzed its effects on the stimulation of human umbilical cord blood-derived mesenchymal stem cells in terms of their potential to differentiate into neuron-like cells, their survival characteristics, and the molecular mechanisms involved. The treatment of cells with neural induction medium (NIM) and BDNF generated more cells that were neuron-like and produced stronger expression of neural-lineage markers than cells treated with NIM and without BDNF. Raf-1 and ERK phosphorylation and p35 expression levels increased significantly in cells treated with both NIM and BDNF. This treatment also effectively blocked cell death following neural induction and increased Akt phosphorylation and Bcl2 expression compared with cells treated with NIM without BDNF. Inhibition of ERKs inhibited the BDNF-stimulated up-regulation of p35 and Bcl2. In addition, the inhibition of PI3K abrogated Akt phosphorylation and Bcl2 expression, but not p35 expression. Thus, MAPK/ERK-dependent p35 up-regulation and MAPK/ERK-dependent and PI3K/Akt-dependent Bcl2 up-regulation contribute to BDNF-stimulated neural differentiation and to the survival of differentiated cells.
机译:脑源性神经营养因子(BDNF)在神经干细胞的分化,发育和存活中起重要作用。在这项研究中,我们就其分化为神经元样细胞的潜力,其存活特征以及涉及的分子机制,分析了其对人脐带血间充质干细胞刺激的影响。与使用NIM和不使用BDNF的细胞相比,用神经诱导培养基(NIM)和BDNF处理的细胞产生了更多的神经元样细胞,并产生更强的神经谱系标记表达。在用NIM和BDNF处理的细胞中,Raf-1和ERK磷酸化以及p35表达水平显着增加。与用不含BDNF的NIM处理的细胞相比,这种处理还可以有效地阻止神经诱导后的细胞死亡,并增加Akt磷酸化和Bcl2表达。抑制ERKs可抑制BDNF刺激的p35和Bcl2的上调。另外,对PI3K的抑制废除了Akt的磷酸化和Bcl2表达,但不废除p35表达。因此,MAPK / ERK依赖的p35上调和MAPK / ERK依赖的和PI3K / Akt依赖的Bcl2上调有助于BDNF刺激的神经分化和分化细胞的存活。

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