成纤维细胞
细胞外基质
细胞生物学
CDC42型
间质细胞
癌症研究
生物
整合素
癌细胞
细胞培养
细胞
激酶
化学
癌相关成纤维细胞
癌症
遗传学
作者
Cédric Gaggioli,Steven Hooper,Cristina Hidalgo-Carcedo,Robert Grosse,John F. Marshall,Kevin J. Harrington,Erik Sahai
摘要
Imaging of collectively invading cocultures of carcinoma cells and stromal fibroblasts reveals that the leading cell is always a fibroblast and that carcinoma cells move within tracks in the extracellular matrix behind the fibroblast. The generation of these tracks by fibroblasts is sufficient to enable the collective invasion of the squamous cell carcinoma (SCC) cells and requires both protease- and force-mediated matrix remodelling. Force-mediated matrix remodelling depends on integrins alpha3 and alpha5, and Rho-mediated regulation of myosin light chain (MLC) activity in fibroblasts, but these factors are not required in carcinoma cells. Instead, carcinoma cells use Cdc42 and MRCK (myotonic dystrophy kinase-related CDC42-binding protein kinases) mediated regulation of MLC to follow the tracks generated by fibroblasts.
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