Fibroblast-led collective invasion of carcinoma cells with differing roles for RhoGTPases in leading and following cells

被引:1162
作者
Gaggioli, Cedric
Hooper, Steven
Hidalgo-Carcedo, Cristina
Grosse, Robert
Marshall, John F.
Harrington, Kevin
Sahai, Erik
机构
[1] Canc Res UK London Res Inst, London WC2A 3PX, England
[2] Heidelberg Univ, Inst Pharmacol, D-69120 Heidelberg, Germany
[3] Barts & London Med & Dent Sch, Queen Marys Coll, Canc Res UK Clin Ctr, Tumour Biol Ctr, London EC1M 6BQ, England
[4] Inst Canc Res, Canc Res UK Ctr Cell & Mol Biol, Chester Beatty Labs, London SW3 6JB, England
关键词
D O I
10.1038/ncb1658
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 alpha 3 and alpha 5, 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.
引用
收藏
页码:1392 / U92
页数:19
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