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Contact Inhibition Of Locomotion In Vivo Controls Neural Crest Directional Migration

机译:体内运动的接触抑制控制神经rest定向迁移

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Contact inhibition of locomotion was discovered by Abercrombie more than 50 years ago and describes the behaviour of fibroblast cells confronting each other in vitro, where they retract their protrusions and change direction on contact. Its failure was suggested to contribute to malignant invasion. However, the molecular basis of contact inhibition of locomotion and whether it also occurs in vivo are still unknown. Here we show that neural crest cells, a highly migratory and multipotent embryonic cell population, whose behaviour has been likened to malignant invasion, demonstrate contact inhibition of locomotion both in vivo and in vitro, and that this accounts for their directional migration. When two migrating neural crest cells meet, they stop, collapse their protrusions and change direction. In contrast, when a neural crest cell meets another cell type, it fails to display contact inhibition of locomotion; instead, it invades the other tissue, in the same manner as metastatic cancer cells. We show that inhibition of non-canonical Wnt signalling abolishes both contact inhibition of locomotion and the directionality of neural crest migration. Wnt-signalling members localize at the site of cell contact, leading to activation of RhoA in this region. These results provide the first example of contact inhibition of locomotion in vivo, provide an explanation for coherent directional migration of groups of cells and establish a previously unknown role for non-canonical Wnt signalling.
机译:接触运动的抑制作用是由Abercrombie于50年前发现的,它描述了成纤维细胞在体外彼此面对的行为,它们在接触时缩回突起并改变方向。它的失败被认为有助于恶性侵袭。然而,尚不清楚接触抑制运动的分子基础以及它是否也发生在体内。在这里,我们显示神经c细胞是一种高度迁移和多能的胚胎细胞群体,其行为被比喻为恶性侵袭,在体内和体外均表现出对运动的接触抑制,这说明了它们的定向迁移。当两个迁移的神经rest细胞相遇时,它们会停下来,折叠其突起并改变方向。相反,当神经rest细胞遇到另一种细胞类型时,它就不能表现出运动的接触抑制。相反,它以与转移癌细胞相同的方式侵入其他组织。我们表明,非经典Wnt信号的抑制消除了运动的接触抑制和神经neural迁移的方向性。 Wnt信号传递成员位于细胞接触部位,导致该区域RhoA激活。这些结果提供了体内运动抑制接触的第一个例子,提供了细胞群相干定向迁移的解释,并为非经典的Wnt信号传导建立了以前未知的作用。

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