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K-ir and K-v channels regulate electrical properties and proliferation of adult neural precursor cells

机译:K-ir和K-v通道调节成年神经前体细胞的电特性和增殖

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The functional significance of the electrophysiological properties of neural precursor cells (NPCs) was investigated using dissociated neurosphere-derived NPCs from the forebrain subventricular zone (SVZ) of adult mice. NPCs exhibited hyperpolarized resting membrane potentials, which were depolarized by the K+ channel inhibitor, Ba2+. Pharmacological analysis revealed two distinct K+ channel families: Ba2+-sensitive K-ir channels and tetraethylammonium (TEA)-sensitive K-v (primarily K-DR) channels. Ba2+ promoted mitogen-stimulated NPC proliferation, which was mimicked by high extracellular K+, whereas TEA inhibited proliferation. Based on gene and protein levels in vitro, we identified K(ir)4.1, K(ir)5.1 and K(v)3.1 channels as the functional W channel candidates. Expression of these K+ channels was immunohistochemically found in NPCs of the adult mouse SVZ, but was negligible in neuroblasts. It therefore appears that expression of Kir and K-v (K-DR) channels in NPCs and related changes in the resting membrane potential could contribute to NPC proliferation and neuronal lineage commitment in the neurogenic microenvironment. (C) 2007 Elsevier Inc. All rights reserved.
机译:使用成年小鼠前脑室下区(SVZ)分离的神经球衍生NPC,研究了神经前体细胞(NPC)的电生理特性的功能意义。 NPC表现出超极化的静息膜电位,该电位被K +通道抑制剂Ba2 +去极化。药理分析揭示了两个不同的K +通道家族:Ba2 +敏感的K-ir通道和四乙铵(TEA)敏感的K-v(主要是K-DR)通道。 Ba2 +促进有丝分裂原刺激的NPC增殖,高细胞外K +模仿了Ba2 +,而TEA抑制了增殖。根据体外基因和蛋白质水平,我们确定了K(ir)4.1,K(ir)5.1和K(v)3.1通道为功能性W通道候选者。这些K +通道的表达在成年小鼠SVZ的NPC中通过免疫组织化学方法发现,但在成神经细胞中可忽略不计。因此看来,NPC中Kir和K-v(K-DR)通道的表达以及静息膜电位的相关变化可能有助于神经源性微环境中NPC的增殖和神经元谱系的定向。 (C)2007 Elsevier Inc.保留所有权利。

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