Down-regulation of Rap1 activity is involved in ephrinB1-induced cell contraction

被引:16
作者
Riedl, JA
Brandt, DT
Batlle, E
Price, LS
Clevers, H
Bos, JL
机构
[1] Univ Utrecht, Med Ctr, Dept Physiol Chem, NL-3584 CG Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Ctr Biomed Genet, NL-3584 CG Utrecht, Netherlands
[3] Ctr Biomed Genet, Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
关键词
contraction; DLD1; cell; down-regulation; EphB2; laminin; Rap1;
D O I
10.1042/BJ20050048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ephrins are cell surface ligands that activate Eph receptor tyrosine kinases. This ligand-receptor interaction plays a central role in the sorting of cells. We have previously shown that the ephrinB-EphB signalling pathway is also involved in the migration of intestinal precursor cells along the crypts. Using the colon cell line DLD1 expressing the EphB2 receptor, we showed that stimulation of these cells with soluble ephrinB1 results in a rapid retraction of cell extensions and a detachment of cells. On ephrinB1 stimulation, the small GTPases Rho and Ras are activated and Rap1 is inactivated. Importantly, when a constitutively active Rap1 mutant was introduced into these cells, ephrinB1-induced retraction was inhibited. From these results, we conclude that down-regulation of Rap1 is a prerequisite for ephrin-induced cell retraction in colon cells.
引用
收藏
页码:465 / 469
页数:5
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