Friedl Peter, Hegerfeldt Yael, Tusch Miriam
Molecular Cell Dynamics Laboratory, Rudolf-Virchow Center, DFG Research Center for Experimental Biomedicine and Department of Dermatology, University of Würzburg, 97089 Würzburg, Germany.
Int J Dev Biol. 2004;48(5-6):441-9. doi: 10.1387/ijdb.041821pf.
The movement of cells that maintain cell-cell junctions yet protrude along or within tissues is an important mechanism for cell positioning in morphogenesis, tissue repair and cancer. Collective cell migration shares similarities but also important differences to individually migrating cells. Coherent groups of cells are arranged and held together by cell-cell adhesion molecules, including cadherins, integrins, ALCAM and NCAM. Integrins of the beta 1 and beta 3 families further provide polarized interactions with the extracellular tissue environment, while matrix-degrading proteases become focalized to substrate contacts to widen tissue space for the advancing cell mass. By generating one functional unit, in contrast to individual cell migration, collective migration provides the active and passive translocation of mobile and non-mobile cells, respectively. This review highlights cellular and molecular principles of collective migration in the context of morphogenic tissue patterning and tumor cell invasion.
细胞在维持细胞间连接的同时沿组织或在组织内突出移动,这是形态发生、组织修复和癌症中细胞定位的重要机制。集体细胞迁移与单个迁移细胞有相似之处,但也有重要差异。细胞通过细胞间粘附分子(包括钙黏蛋白、整合素、活化白细胞黏附分子和神经细胞黏附分子)排列并聚集在一起。β1和β3家族的整合素进一步与细胞外组织环境提供极化相互作用,而基质降解蛋白酶则集中于底物接触部位,为前进的细胞团扩大组织空间。与单个细胞迁移相比,集体迁移通过产生一个功能单元,分别提供了移动细胞和非移动细胞的主动和被动转运。本综述重点介绍了形态发生组织模式形成和肿瘤细胞侵袭背景下集体迁移的细胞和分子原理。