Spatiotemporal dynamics of RhoA activity in migrating cells

被引:622
作者
Pertz, O [1 ]
Hodgson, L
Klemke, RL
Hahn, KM
机构
[1] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Canc Ctr, Chapel Hill, NC 27599 USA
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature04665
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rho family GTPases regulate the actin and adhesion dynamics that control cell migration. Current models postulate that Rac promotes membrane protrusion at the leading edge and that RhoA regulates contractility in the cell body(1,2). However, there is evidence that RhoA also regulates membrane protrusion(3,4). Here we use a fluorescent biosensor, based on a novel design preserving reversible membrane interactions, to visualize the spatiotemporal dynamics of RhoA activity during cell migration. In randomly migrating cells, RhoA activity is concentrated in a sharp band directly at the edge of protrusions. It is observed sporadically in retracting tails, and is low in the cell body. RhoA activity is also associated with peripheral ruffles and pinocytic vesicles, but not with dorsal ruffles induced by platelet-derived growth factor (PDGF). In contrast to randomly migrating cells, PDGF-induced membrane protrusions have low RhoA activity, potentially because PDGF strongly activates Rac, which has previously been shown to antagonize RhoA activity(5,6). Our data therefore show that different extracellular cues induce distinct patterns of RhoA signalling during membrane protrusion.
引用
收藏
页码:1069 / 1072
页数:4
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