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Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway

机译:血色素是成人在脑室下区域/嗅球通路中发生神经形成所必需的

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摘要

The neural stem cells (NSCs) of the subventricular zone (SVZ) reside within a specialized niche critical for neurogenesis. Hemopexin, a plasma glycoprotein, has been extensively studied as a heme scavenger at the systemic level. However, little is known about its function in the central nervous system, especially in neurogenesis. In the present study, we demonstrate that deletion of hemopexin leads to neurogenic abnormalities in the SVZ/olfactory bulb (OB) pathway. The lateral ventricle is enlarged in hemopexin-deficient mice, and more apoptosis was observed in Dcx+ cells. Lineage differentiation of NSCs was also inhibited in the SVZ of hemopexin-deficient mice, with more stem cells stayed in an undifferentiated, GFAP+ radial glia-like cell stage. Moreover, hemopexin deletion resulted in impaired neuroblast migration in the rostral migratory stream. Furthermore, exogenous hemopexin protein inhibited apoptosis and promoted the migration and differentiation of cultured NSCs. Finally, immunohistochemical analysis demonstrated that deletion of hemopexin reduced the number of interneurons in the OB. Together, these results suggest a new molecular mechanism for the NSC niche that regulates adult neurogenesis in the SVZ/OB pathway. Our findings may benefit the understanding for olfactory system development.
机译:脑室下区域(SVZ)的神经干细胞(NSC)驻留在对神经发生至关重要的专门小生境中。血凝素是一种血浆糖蛋白,已在系统水平上作为血红素清除剂进行了广泛研究。然而,人们对其在中枢神经系统中的功能知之甚少,特别是在神经发生中。在本研究中,我们证明了血红蛋白的删除导致SVZ /嗅球(OB)通路中的神经源性异常。血红素缺乏症小鼠的侧脑室增大,在Dcx +细胞中观察到更多的凋亡。 NSC的谱系分化在血红蛋白缺乏症小鼠的SVZ中也受到抑制,更多的干细胞停留在未分化的GFAP +放射状胶质样细胞阶段。此外,血红素蛋白的缺失导致在延髓流中神经母细胞迁移受损。此外,外源性血红蛋白抑制细胞凋亡,并促进培养的神经干细胞的迁移和分化。最后,免疫组织化学分析表明血红蛋白的删除减少了OB中的内部神经元的数量。总之,这些结果表明,NSC利基的新分子机制可调节SVZ / OB途径中的成年神经发生。我们的发现可能有助于理解嗅觉系统的发育。

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