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神经嵴迁移起始过程中细胞黏附和运动的调控。

Regulation of cell adhesions and motility during initiation of neural crest migration.

机构信息

Department of Zoology, 1117 W. Johnson Street, Madison, WI 53706, USA.

出版信息

Curr Opin Neurobiol. 2011 Feb;21(1):17-22. doi: 10.1016/j.conb.2010.09.013. Epub 2010 Oct 21.

Abstract

Accurate neural crest cell (NCC) migration requires tight control of cell adhesions, cytoskeletal dynamics and cell motility. Cadherins and RhoGTPases are critical molecular players that regulate adhesions and motility during initial delamination of NCCs from the neuroepithelium. Recent studies have revealed multiple functions for these molecules and suggest that a precise balance of their activity is crucial. RhoGTPase appears to regulate both cell adhesions and protrusive forces during NCC delamination. Increasing evidence shows that cadherins are multi-functional proteins with novel, adhesion-independent signaling functions that control NCC motility during both delamination and migration. These functions are often regulated by specific proteolytic cleavage of cadherins. After NCC delamination, planar cell polarity signaling acts via RhoGTPases to control NCC protrusions and migration direction.

摘要

准确的神经嵴细胞(NCC)迁移需要严格控制细胞黏附、细胞骨架动力学和细胞迁移。钙黏蛋白和 RhoGTPases 是调控 NCC 从神经上皮初始分层过程中黏附和迁移的关键分子。最近的研究揭示了这些分子的多种功能,并表明它们的活性精确平衡至关重要。RhoGTPase 似乎在 NCC 分层过程中调节细胞黏附和突起力。越来越多的证据表明,钙黏蛋白是多功能蛋白,具有新型的、不依赖黏附的信号功能,可控制 NCC 在分层和迁移过程中的运动。这些功能通常受钙黏蛋白的特定蛋白水解切割调节。NCC 分层后,平面细胞极性信号通过 RhoGTPases 控制 NCC 突起和迁移方向。

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