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MARK2/Par-1 guides the directionality of neuroblasts migrating to the olfactory bulb

机译:MARK2 / Par-1指导成神经细胞迁移至嗅球的方向性

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In rodents and most other mammals studied, neuronal precursors generated in the subventricular zone (SVZ) migrate to the adult olfactory bulb (OB) to differentiate into interneurons called granule and periglomerular cells. How the newborn cells navigate in the postnatal forebrain to reach precisely their target area is largely unknown. However, it is often thought that postnatal neurogenesis recapitulates the neuronal development occurring during embryogenesis. During brain development, intracellular kinases are key elements for controlling cell polarization as well as the coupling between polarization and cellular movement. We show here that the polarity kinase MARK2 maintains its expression in the postnatal SVZ-OB system. We therefore investigated the potential role of this kinase in adjusting postnatal neuroblast migration. We employed mouse brain slices maintained in culture, in combination with lentiviral vector injections designed to label neuronal precursors with GFP and to diminish the expression of MARK2. Time-lapse video microscopy was used to monitor neuroblast migration in the postnatal forebrain from SVZ precursors to cells populating the OB. We found that reduced MARK2 expression resulted in altered migratory patterns and stalled neuroblasts in the rostral migratory stream (RMS). In agreement with the observed migratory defects, we report a diminution of the proportion of cells reaching the OB layers. Our study reveals the involvement of MARK2 in the maintenance of the migratory direction in postnatally-generated neuroblasts and consequently on the control of the number of newly-generated neurons reaching and integrating the appropriate target circuits.
机译:在啮齿动物和大多数其他研究过的哺乳动物中,在脑室下区域(SVZ)中产生的神经元前体迁移到成年嗅球(OB),以分化为称为颗粒和肾小球周围细胞的中间神经元。新生细胞如何在产后前脑中导航以精确到达其目标区域尚不清楚。然而,通常认为,产后神经发生可概括胚胎发生期间发生的神经元发育。在大脑发育过程中,细胞内激酶是控制细胞极化以及极化与细胞运动之间耦合的关键元素。我们在这里显示极性激酶MARK2在产后SVZ-OB系统中保持其表达。因此,我们研究了该激酶在调节出生后神经母细胞迁移中的潜在作用。我们采用了维持培养的小鼠脑切片,并结合了慢病毒载体注射剂,设计以GFP标记神经元前体并减少MARK2的表达。延时视频显微镜用于监测产后前脑中的成神经细胞从SVZ前体迁移到组成OB的细胞。我们发现减少的MARK2表达导致迁移的模式和延缓的延髓流(RMS)中的成神经细胞停滞。与观察到的迁移缺陷一致,我们报告了到达OB层的细胞比例减少。我们的研究揭示了MARK2参与维持产后生成的神经母细胞的迁移方向,从而控制了到达并整合适当靶电路的新生神经元的数量。

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