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Laminin regulates postnatal oligodendrocyte production by promoting oligodendrocyte progenitor survival in the subventricular zone

机译:层粘连蛋白通过促进脑室下区少突胶质细胞祖细胞的存活来调节产后少突胶质细胞的产生

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The laminin family of extracellular matrix proteins are expressed broadly during embryonic brain development, but are enriched at ventricular and pial surfaces where laminins mediate radial glial attachment during corticogenesis. In the adult brain, however, laminin distribution is restricted, yet is found within the vascular basal lamina and associated fractones of the ventricular zone (VZ)-subventricular zone (SVZ) stem cell niche, where laminins regulate adult neural progenitor cell proliferation. It remains unknown, however, if laminins regulate the wave of oligodendrogenesis that occurs in the neonatal/early postnatal VZ-SVZ. Here we report that Lama2, the gene that encodes the laminin α2-subunit, regulates postnatal oligodendrogenesis. At birth, Lama2-/- mice had significantly higher levels of dying oligodendrocyte progenitor cells (OPCs) in the OPC germinal zone of the dorsal SVZ. This translated into fewer OPCs, both in the dorsal SVZ well as in an adjacent developing white matter tract, the corpus callosum. In addition, intermediate progenitor cells that give rise to OPCs in the Lama2-/- VZ-SVZ were mislocalized and proliferated nearer to the ventricle surface. Later, delays in oligodendrocyte maturation (with accompanying OPC accumulation), were observed in the Lama2-/- corpus callosum, leading to dysmyelination by postnatal day 21. Together these data suggest that prosurvival laminin interactions in the developing postnatal VZ-SVZ germinal zone regulate the ability, or timing, of oligodendrocyte production to occur appropriately.
机译:层粘连蛋白细胞外基质蛋白家族在胚胎脑发育过程中广泛表达,但在皮层生成过程中,层粘连蛋白介导radial神经胶质附着的心室和皮层表面富集。然而,在成年大脑中,层粘连蛋白的分布受到限制,但仍在血管基底层和心室区(VZ)-心室下区(SVZ)干细胞生态位的相关分形内发现,层粘连蛋白调节着成人神经祖细胞的增殖。但是,层粘连蛋白是否能调节新生/初生后VZ-SVZ中发生的少突胶质生成波仍然未知。在这里我们报告说,编码层粘连蛋白α2亚基的基因Lama2调节产后少突胶质生成。在出生时,Lama2-/-小鼠在背侧SVZ的OPC生发区中的垂死性少突胶质细胞祖细胞(OPC)的水平明显较高。在背侧SVZ和相邻的发育中的白质束体中,这转化为更少的OPC。此外,在Lama2-/-VZ-SVZ中产生OPC的中间祖细胞位置不正确,并在靠近心室表面的位置增殖。后来,在Lama2-/-call体中观察到少突胶质细胞成熟的延迟(伴随OPC积累),导致在出生后第21天发生髓鞘脱髓鞘。这些数据共同表明,正在发展的出生后VZ-SVZ生发区中的存活层粘连蛋白相互作用少突胶质细胞产生的能力或时机。

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