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Intracellular Nitric Oxide Mediates Neuroproliferative Effect of Neuropeptide Y on Postnatal Hippocampal Precursor Cells

机译:细胞内一氧化氮介导神经肽Y对产后海马前体细胞的神经增殖作用

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摘要

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.
机译:神经肽Y(NPY)在中枢神经系统和周围神经系统中广泛表达,并在体外对多种细胞类型具有增殖作用。 NPY在基础和病理条件下均在体内调节成人海马神经发生中起关键作用,尽管其基本机制尚不清楚。我们已经研究了一氧化氮(NO)在NPY的神经源性作用中的作用。使用产后大鼠海马培养物,我们表明NPY对nestin + 前体细胞的增殖作用是NO依赖性的。除了涉及神经元一氧化氮合酶外,增殖作用还通过一氧化氮/环鸟苷单磷酸(cGMP)/依赖于cGMP的蛋白激酶(PKG)和细胞外信号调节激酶(ERK)1/2信号通路来介导。我们表明,NPY介导的细胞内NO信号导致神经增殖的增加。相反,细胞外NO对增殖具有相反的抑制作用。使用蛋白质印迹证实了NO-cGMP-PKG信号通路在ERK1 / 2激活中的重要性。这项工作将两个重要的海马神经发生调节剂整合在一个共同的信号传递框架内,并提供了一种机制,用于通过NO对产后神经前体进行独立的细胞外和细胞内调节。

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