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Ephrin B1 maintains apical adhesion of neural progenitors

机译:Ephrin B1维持神经祖细胞的根尖黏附

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Apical neural progenitors are polarized cells for which the apical membrane is the site of cell-cell and cell-extracellular matrix adhesion events that are essential for maintaining the integrity of the developing neuroepithelium. Apical adhesion is important for several aspects of the nervous system development, including morphogenesis and neurogenesis, yet the mechanisms underlying its regulation remain poorly understood. Here, we show that ephrin B1, a cell surface protein that engages in cell signaling upon binding cognate Eph receptors, controls normal morphogenesis of the developing cortex. Efnb1-deficient embryos exhibit morphological alterations of the neuroepithelium that correlate with neural tube closure defects. Using loss-of-function experiments by ex vivo electroporation, we demonstrate that ephrin B1 is required in apical progenitors (APs) to maintain their apical adhesion. Mechanistically, we show that ephrin B1 controls cell-ECM adhesion by promoting apical localization of integrin β1 and we identify ADP-ribosylation factor 6 (Arf6) as an important effector of ephrin B1 reverse signaling in apical adhesion of APs. Our results provide evidence for an important role for ephrin B1 in maintaining the structural integrity of the developing cortex and highlight the importance of tightly controlling apical cell-ECM adhesion for neuroepithelial development.
机译:顶神经祖细胞是极化细胞,其顶膜是细胞-细胞和细胞-细胞外基质粘附事件的部位,这对于维持发育中的神经上皮的完整性至关重要。根尖粘连对于神经系统发育的几个方面都很重要,包括形态发生和神经发生,但其调控机制尚不清楚。在这里,我们显示ephrin B1,一种细胞表面蛋白,在结合相关的Eph受体后参与细胞信号传导,控制着发育中的皮层的正常形态发生。缺乏Efnb1的胚胎表现出与神经管闭合缺陷相关的神经上皮形态改变。使用离体电穿孔功能丧失的实验,我们证明了ephrin B1是根尖祖细胞(APs)所必需的,以维持其根尖粘附。从机制上讲,我们表明ephrin B1通过促进整联蛋白β1的根尖定位来控制细胞-ECM粘附,并且我们确定ADP-核糖基化因子6(Arf6)是ephrin B1反向信号在APs粘附中的重要作用。我们的结果提供了证据,表明ephrin B1在维持发育中的皮层的结构完整性中起着重要作用,并强调了紧密控制根尖细胞-ECM粘附对于神经上皮发育的重要性。

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