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鉴定载脂蛋白 E 作为一种自分泌/旁分泌因子,通过 MAPK/ERK 信号通路刺激神经干细胞存活。

Identification of ApoE as an autocrine/paracrine factor that stimulates neural stem cell survival via MAPK/ERK signaling pathway.

机构信息

Neural Stem Cell Laboratory, Institute of Medical Biology, Singapore.

出版信息

J Neurochem. 2011 May;117(3):565-78. doi: 10.1111/j.1471-4159.2011.07227.x. Epub 2011 Mar 21.

Abstract

Neural stem cells (NSCs) are self-renewing multipotent cells that undergo symmetric and asymmetric cell division during development of the nervous system. The behavior of NSCs is tightly regulated by intrinsic processes such as transcriptional and post-transcriptional control, as well as the stem cell niche factors that activate ligand-receptor-mediated signaling pathways. However, the role of these niche factors that regulate NSC behavior is not clearly understood. We identified chondroitin sulfate proteoglycan, apolipoprotein E (ApoE) and cystatin C as factors derived from the mouse neurosphere conditioned medium. Here, we show that ApoE is an autocrine/paracrine factor that regulates NSC survival. Stimulation of NSC survival is mediated by ApoE receptor interaction and the downstream extracellular signal-regulated kinase/mitogen-activated protein kinase signaling pathway. In addition, ApoE also enhanced neurosphere formation of mouse embryonic stem cell-derived NSCs. Finally, in vitro differentiation studies with ApoE knock-out NSCs suggest a role for ApoE in oligodendrogenesis.

摘要

神经干细胞(NSCs)是自我更新的多能细胞,在神经系统发育过程中经历对称和不对称细胞分裂。NSCs 的行为受到内在过程的严格调控,如转录和转录后控制,以及激活配体-受体介导的信号通路的干细胞生态位因子。然而,调节 NSCs 行为的这些生态位因子的作用尚不清楚。我们确定了软骨素硫酸盐蛋白聚糖、载脂蛋白 E(ApoE)和半胱氨酸蛋白酶抑制剂 C 是源自小鼠神经球条件培养基的因子。在这里,我们表明 ApoE 是一种旁分泌/自分泌因子,可调节 NSCs 的存活。NSC 存活的刺激是通过 ApoE 受体相互作用和下游细胞外信号调节激酶/丝裂原活化蛋白激酶信号通路介导的。此外,ApoE 还增强了小鼠胚胎干细胞衍生 NSCs 的神经球形成。最后,用 ApoE 敲除 NSCs 进行的体外分化研究表明 ApoE 在少突胶质细胞形成中起作用。

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