Raich W B, Agbunag C, Hardin J
Program in Cellular and Molecular Biology University of Wisconsin-Madison 1117 W Johnson Street, Madison, Wisconsin, 53706, USA.
Curr Biol. 1999 Oct 21;9(20):1139-46. doi: 10.1016/S0960-9822(00)80015-9.
During embryonic development, epithelia with free edges must join together to create continuous tissues that seal the interior of the organism from the outside environment; failure of epithelial sealing underlies several common human birth defects. Sealing of epithelial sheets in embryos can be extremely rapid, dramatically exceeding the rate of adherens junction formation by epithelial cells in culture or during healing of epithelial wounds. Little is known about the dynamic redistribution of cellular junctional components during such events in living embryos.
We have used time-lapse, multiphoton laser-scanning microscopy and green fluorescent protein fusion proteins to analyze the sealing of the Caenorhabditis elegans epidermis in living embryos. Rapid recruitment of alpha-catenin to sites of filopodial contact between contralateral migrating epithelial cells, concomitant with clearing of cytoplasmic alpha-catenin, resulted in formation of nascent junctions; this preceded the formation of mature junctions. Surprisingly, upon inactivation of the entire cadherin-catenin complex, only adhesive strengthening between filopodia was reproducibly affected. Other ventral epidermal cells, which did not extend filopodia and appeared to seal along the ventral midline by coordinated changes in cell shape, successfully adhered in the absence of these proteins.
We propose that 'filopodial priming' - prealignment of bundled actin in filopodia combined with the rapid recruitment of alpha-catenin from cytoplasmic reserves at sites of filopodial contact - accounts for the rapid rate of sealing of the embryonic epidermis of C. elegans. Filopodial priming may provide a general mechanism for rapid creation of adherens junctions during epithelial-sheet sealing in embryos.
在胚胎发育过程中,具有自由边缘的上皮细胞必须连接在一起,形成连续的组织,将生物体内部与外部环境隔离开来;上皮细胞密封失败是几种常见人类出生缺陷的根本原因。胚胎中上皮细胞层的密封可能极其迅速,大大超过培养中的上皮细胞或上皮伤口愈合过程中黏附连接形成的速度。对于活胚胎中此类事件期间细胞连接成分的动态重新分布,人们了解甚少。
我们使用延时多光子激光扫描显微镜和绿色荧光蛋白融合蛋白来分析活胚胎中秀丽隐杆线虫表皮的密封过程。α-连环蛋白迅速募集到对侧迁移的上皮细胞之间丝状伪足接触的部位,同时细胞质中的α-连环蛋白清除,导致新生连接的形成;这先于成熟连接的形成。令人惊讶的是,当整个钙黏蛋白-连环蛋白复合物失活时,只有丝状伪足之间的黏附增强受到可重复的影响。其他腹侧表皮细胞,它们不伸出丝状伪足,似乎通过细胞形状的协调变化沿腹中线密封,在没有这些蛋白质的情况下成功黏附。
我们提出“丝状伪足引发”——丝状伪足中肌动蛋白束的预排列,结合丝状伪足接触部位细胞质储备中α-连环蛋白的快速募集——解释了秀丽隐杆线虫胚胎表皮快速密封的速度。丝状伪足引发可能为胚胎上皮细胞层密封过程中快速形成黏附连接提供一种普遍机制。