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在PC12细胞分化过程中,骨形态发生蛋白(BMP)增强了对神经生长因子(NGF)的转录反应。

BMP enhances transcriptional responses to NGF during PC12 cell differentiation.

作者信息

Lönn P, Zaia K, Israelsson C, Althini S, Usoskin D, Kylberg A, Ebendal T

机构信息

Department of Neuroscience, Uppsala University, Biomedical Center, Box 587, SE 751 23, Uppsala, Sweden.

出版信息

Neurochem Res. 2005 Jun-Jul;30(6-7):753-65. doi: 10.1007/s11064-005-6868-6.

Abstract

Bone morphogenetic proteins (BMPs) enhance neurite outgrowth in nerve growth factor (NGF)-stimulated PC12 cells. To investigate the mechanism of this potentiating effect, real-time PCR was used to analyze the expression of 45 selected genes. A robust increase in expression of 10 immediate early genes including Egr1-4, Hes1, Junb, Jun and Fos was observed already after 1 h treatment with NGF alone. NGF plus BMP4 further increased these transcripts at 1 h and activated 18 additional genes. BMP4 alone induced Smad6, Mtap1b and Hes1. Egr3 was the gene most strongly upregulated by NGF and BMP4. However, luciferase assays showed that the cloned Egr3 proximal promoter was not involved in the BMP4 potentiation. Blocking Egr3 and Junb function by dominant-negative constructs reduced neurite outgrowth under stimulating conditions, proving that activation of members of both the Egr and Jun families is necessary for maximal PC12 cell response to NGF and BMP4.

摘要

骨形态发生蛋白(BMPs)可增强神经生长因子(NGF)刺激的PC12细胞中的神经突生长。为了研究这种增强作用的机制,采用实时PCR分析了45个选定基因的表达。仅用NGF处理1小时后,就观察到包括Egr1 - 4、Hes1、Junb、Jun和Fos在内的10个立即早期基因的表达显著增加。NGF加BMP4在1小时时进一步增加了这些转录本,并激活了另外18个基因。单独的BMP4诱导了Smad6、Mtap1b和Hes1。Egr3是受NGF和BMP4上调最强烈的基因。然而,荧光素酶测定表明,克隆的Egr3近端启动子不参与BMP4的增强作用。通过显性负性构建体阻断Egr3和Junb的功能会降低刺激条件下的神经突生长,证明Egr和Jun家族成员的激活对于PC12细胞对NGF和BMP4的最大反应是必要的。

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