Trading spaces: Rap, Rac, and Rho as architects of transendothelial migration

细胞生物学 GTP酶 生物 Rap1型 RAC1 细胞粘附 调节器 内皮干细胞 激酶 细胞迁移 小型GTPase 整合素 信号转导 细胞 生物化学 基因 体外
作者
Erika S. Wittchen,Jaap D. van Buul,Keith Burridge,Rebecca A. Worthylake
出处
期刊:Current Opinion in Hematology [Ovid Technologies (Wolters Kluwer)]
卷期号:12 (1): 14-21 被引量:74
标识
DOI:10.1097/01.moh.0000147892.83713.a7
摘要

This review focuses on recent developments in understanding regulation of leukocyte transendothelial migration by small GTPase signaling.New studies are refining the model for GTPase regulation of leukocyte-endothelial cell interactions that occur during leukocyte transmigration. An emerging theme is that the endothelial cell is an active participant in this process; an example of this is the identification of a novel leukocyte docking structure. The role of second messengers such as reactive oxygen species downstream and the involvement of kinases such as Pyk2 and Tec kinases upstream of GTPase activation is becoming appreciated. In the leukocyte, finer distinctions between closely related GTPases like Rac1 and Rac2 are being made, and a new role for RhoH has been characterized. Finally, the focus on Rap1 as a key regulator of leukocyte integrin-dependent adhesion is expanding to include roles in endothelial cell-cell adhesion and junctional regulation during transmigration.Understanding the complex series of events involved in cell-cell interactions during leukocyte transendothelial migration is a prerequisite for designing novel therapies to treat clinical conditions in which an inappropriate inflammatory response leads to disease. A discussion is provided of recent developments in the molecular regulation of leukocyte recruitment.
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