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细胞内一氧化氮介导神经肽 Y 对出生后海马前体细胞的神经增殖作用。

Intracellular nitric oxide mediates neuroproliferative effect of neuropeptide y on postnatal hippocampal precursor cells.

机构信息

Division of Clinical Neurosciences, University of Southampton, Southampton SO17 1BJ, United Kingdom.

出版信息

J Biol Chem. 2012 Jun 8;287(24):20187-96. doi: 10.1074/jbc.M112.346783. Epub 2012 Apr 3.

Abstract

Neuropeptide Y (NPY) is widely expressed in the central and peripheral nervous systems and is proliferative for a range of cells types in vitro. NPY plays a key role in regulating adult hippocampal neurogenesis in vivo under both basal and pathological conditions, although the underlying mechanisms are largely unknown. We have investigated the role of nitric oxide (NO) on the neurogenic effects of NPY. Using postnatal rat hippocampal cultures, we show that the proliferative effect of NPY on nestin(+) precursor cells is NO-dependent. As well as the involvement of neuronal nitric-oxide synthase, the proliferative effect is mediated via an NO/cyclic guanosine monophosphate (cGMP)/cGMP-dependent protein kinase (PKG) and extracellular signal-regulated kinase (ERK) 1/2 signaling pathway. We show that NPY-mediated intracellular NO signaling results in an increase in neuroproliferation. By contrast, extracellular NO had an opposite, inhibitory effect on proliferation. The importance of the NO-cGMP-PKG signaling pathway in ERK1/2 activation was confirmed using Western blotting. This work unites two significant modulators of hippocampal neurogenesis within a common signaling framework and provides a mechanism for the independent extra- and intracellular regulation of postnatal neural precursors by NO.

摘要

神经肽 Y(NPY)广泛表达于中枢和外周神经系统,在体外对多种细胞类型具有增殖作用。NPY 在体内的基础和病理条件下对成年海马神经发生起关键作用,但其潜在机制在很大程度上尚不清楚。我们研究了一氧化氮(NO)对 NPY 的神经发生作用的影响。我们使用出生后大鼠海马培养物表明,NPY 对巢蛋白(+)前体细胞的增殖作用依赖于 NO。除神经元型一氧化氮合酶(nNOS)的参与外,该增殖作用还通过 NO/环鸟苷酸(cGMP)/cGMP 依赖性蛋白激酶(PKG)和细胞外信号调节激酶(ERK)1/2 信号通路介导。我们表明,NPY 介导的细胞内 NO 信号导致神经增殖增加。相比之下,细胞外 NO 对增殖有相反的抑制作用。使用 Western blot 验证了 NO-cGMP-PKG 信号通路在 ERK1/2 激活中的重要性。这项工作将海马神经发生的两个重要调节剂统一在一个共同的信号框架内,并为 NO 对出生后神经前体细胞的独立细胞内外调节提供了一种机制。

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