首页> 美国卫生研究院文献>The Journal of Neuroscience >The Ciliary Neurotrophic Factor/Leukemia Inhibitory Factor/gp130 Receptor Complex Operates in the Maintenance of Mammalian Forebrain Neural Stem Cells
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The Ciliary Neurotrophic Factor/Leukemia Inhibitory Factor/gp130 Receptor Complex Operates in the Maintenance of Mammalian Forebrain Neural Stem Cells

机译:睫状神经营养因子/白血病抑制因子/ gp130受体复合物在哺乳动物前脑神经干细胞的维持中发挥作用。

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摘要

The cytokines that signal through the common receptor subunit gp130, including ciliary neurotrophic factor (CNTF), interleukin-6, leukemia inhibitory factor (LIF) and oncostatin M, have pleiotropic functions in CNS development. Given the restricted expression domain of the CNTF receptor α (CNTFR) in the developing forebrain germinal zone and adult forebrain periventricular area, we have examined the putative role of CNTFR/LIFR/gp130-mediated signaling in regulating forebrain neural stem cell fate in vivo and in vitro. Analysis ofLIFR-deficient mice revealed that a decreased level of LIFR expression results in a reduction in the number of adult neural stem cells. In adult LIFR heterozygote (+/−) mice, the number of neural stem cells and their progeny in the forebrain subependyma and TH-immunoreactive neurons in the olfactory bulb were significantly reduced. Intraventricular infusion of CNTF into the adult mouse forebrain, in the absence or presence of epidermal growth factor (EGF), enhanced self-renewal of neural stem cells in vivo. Analyses of EGF-responsive neural stem cells proliferating in vitro found that CNTF inhibits lineage restriction of neural stem cells to glial progenitors, which in turn results in enhanced expansion of stem cell number. These results suggest that CNTFR/LIFR/gp130-mediated signaling supports the maintenance of forebrain neural stem cells, likely by suppressing restriction to a glial progenitor cell fate.
机译:通过共同受体亚基gp130发出信号的细胞因子,包括睫状神经营养因子(CNTF),白细胞介素6,白血病抑制因子(LIF)和抑癌素M,在CNS发育中具有多效性功能。鉴于CNTF受体α(CNTFR)在发育中的前脑生发区和成年前脑室周围区域中的表达域受限制,我们已经研究了CNTFR / LIFR / gp130介导的信号传导在体内调节前脑神经干细胞命运的假定作用,体外。对LIFR缺陷型小鼠的分析表明,LIFR表达水平的降低导致成年神经干细胞数量的减少。在成年LIFR杂合子(+/-)小鼠中,前脑室管膜下神经干细胞的数量及其后代以及嗅球中TH免疫反应性神经元的数量均明显减少。在不存在或存在表皮生长因子(EGF)的情况下,向成年小鼠前脑室内注入CNTF可以增强体内神经干细胞的自我更新能力。对EGF反应性神经干细胞体外增殖的分析发现,CNTF抑制了神经干细胞向神经胶质祖细胞的谱系限制,进而导致干细胞数量的增加。这些结果表明,CNTFR / LIFR / gp130介导的信号传导可能通过抑制对神经胶质祖细胞命运的限制来支持前脑神经干细胞的维持。

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