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肠神经母细胞需要磷脂酰肌醇3激酶/蛋白激酶B/叉头框蛋白途径来实现胶质细胞源性神经营养因子刺激的存活。

Enteric neuroblasts require the phosphatidylinositol 3-kinase/Akt/Forkhead pathway for GDNF-stimulated survival.

作者信息

Srinivasan Shanthi, Anitha Mallappa, Mwangi Simon, Heuckeroth Robert O

机构信息

Department of Medicine, Division of Digestive Diseases, Emory University, 615 Michael Street, Whitehead Research Building, Suite 246, Atlanta, GA 30322, USA.

出版信息

Mol Cell Neurosci. 2005 May;29(1):107-19. doi: 10.1016/j.mcn.2005.02.005.

Abstract

Glial cell line-derived neurotrophic factor (GDNF)/Ret signaling is required for enteric neural crest survival, proliferation, migration and process extension, but signaling pathways that mediate enteric nervous system (ENS) precursor development are poorly understood. We therefore examined GDNF effects on immunoselected ENS precursor survival and neuronal process extension in the presence of phosphatidylinositol 3-kinase and mitogen-activated protein kinase pathway inhibitors. These studies demonstrated that GDNF promotes ENS precursor survival through phosphatidylinositol-3-kinase. Specifically, GDNF induces phosphorylation of Akt and loss of the Akt substrates FOXO1 and FOXO3a from the nucleus of ENS precursors. Furthermore, dominant negative Akt or active FOXO1 constructs promote ENS precursor cell death while a dominant negative FOXO1 construct prevents cell death. In contrast, the MAPK kinase inhibitor PD98059 did not influence ENS precursor survival or neurite extension. These data demonstrate a critical role for PI-3 kinase/Akt/FOXO signaling, but not for MAPK in ENS precursor survival and neurite extension.

摘要

胶质细胞系源性神经营养因子(GDNF)/Ret信号传导对于肠神经嵴的存活、增殖、迁移和轴突生长是必需的,但介导肠神经系统(ENS)前体发育的信号通路仍知之甚少。因此,我们在磷脂酰肌醇3激酶和丝裂原活化蛋白激酶通路抑制剂存在的情况下,研究了GDNF对免疫筛选的ENS前体存活和神经元轴突生长的影响。这些研究表明,GDNF通过磷脂酰肌醇-3激酶促进ENS前体的存活。具体而言,GDNF诱导Akt磷酸化,并使ENS前体细胞核中的Akt底物FOXO1和FOXO3a缺失。此外,显性负性Akt或活性FOXO1构建体促进ENS前体细胞死亡,而显性负性FOXO1构建体则可防止细胞死亡。相比之下,MAPK激酶抑制剂PD98059不影响ENS前体的存活或神经突生长。这些数据表明PI-3激酶/Akt/FOXO信号传导在ENS前体存活和神经突生长中起关键作用,而MAPK则不起作用。

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