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垂体腺苷酸环化酶激活多肽通过激活Ras和Rap1刺激皮质前体细胞中的胶质纤维酸性蛋白基因表达。

Pituitary adenylate cyclase-activating polypeptide stimulates glial fibrillary acidic protein gene expression in cortical precursor cells by activating Ras and Rap1.

作者信息

Lastres-Becker Isabel, Fernández-Pérez Antonio, Cebolla Beatriz, Vallejo Mario

机构信息

Instituto de Investigaciones Biomédicas Alberto Sols, Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, Spain.

出版信息

Mol Cell Neurosci. 2008 Nov;39(3):291-301. doi: 10.1016/j.mcn.2008.07.009. Epub 2008 Jul 29.

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) acts on cortical precursor cells to trigger glial fibrillary acidic protein (GFAP) gene expression and astrocyte differentiation by stimulation of intracellular cAMP production. Here, we show that as expected, PACAP activates cAMP-dependent protein kinase A. However, inhibition of protein kinase A does not prevent PACAP-induced GFAP gene expression or astrocytogenesis. PACAP also activates the small GTPases Rap1 and Ras, but either activation of Rap1 alone by selective stimulation of the guanine nucleotide exchange factor Epac, or expression of a constitutively active form of Ras, do not induce GFAP gene expression. Ras is activated by PACAP in a cAMP-dependent manner, and inhibition of Ras and/or Rap1 decreases PACAP-induced GFAP promoter stimulation. Thus, cAMP-dependent PACAP-induced GFAP expression during astrocytogenesis involves the coordinated activation of both Ras and Rap1, but activation of either one of them in isolation is not sufficient to trigger this response.

摘要

垂体腺苷酸环化酶激活多肽(PACAP)作用于皮质前体细胞,通过刺激细胞内cAMP生成来触发胶质纤维酸性蛋白(GFAP)基因表达和星形胶质细胞分化。在此,我们发现,正如预期的那样,PACAP激活了cAMP依赖性蛋白激酶A。然而,抑制蛋白激酶A并不能阻止PACAP诱导的GFAP基因表达或星形胶质细胞生成。PACAP还激活小GTP酶Rap1和Ras,但单独通过选择性刺激鸟嘌呤核苷酸交换因子Epac激活Rap1,或表达Ras的组成型活性形式,均不会诱导GFAP基因表达。Ras以cAMP依赖性方式被PACAP激活,抑制Ras和/或Rap1会降低PACAP诱导的GFAP启动子刺激。因此,在星形胶质细胞生成过程中,cAMP依赖性PACAP诱导的GFAP表达涉及Ras和Rap1的协同激活,但单独激活其中任何一个都不足以触发这种反应。

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