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Eur J Cell Biol. 2013 Oct-Nov;92(10-11):303-15. doi: 10.1016/j.ejcb.2013.09.002. Epub 2013 Oct 8.

Physiological roles of Rho and Rho effectors in mammals.

Author information

1
Department of Pharmacology, Kyoto University Faculty of Medicine, Sakyo-ku, Kyoto 606-8501, Japan; Innovation Center for Immunoregulation, Technologies and Drugs (AK Project), Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto 606-8501, Japan. Electronic address: d.thumkeo@mfour.med.kyoto-u.ac.jp.

Abstract

Rho GTPase is a master regulator controlling cytoskeleton in multiple contexts such as cell migration, adhesion and cytokinesis. Of several Rho GTPases in mammals, the best characterized is the Rho subfamily including ubiquitously expressed RhoA and its homologs RhoB and RhoC. Upon binding GTP, Rho exerts its functions through downstream Rho effectors, such as ROCK, mDia, Citron, PKN, Rhophilin and Rhotekin. Until recently, our knowledge about functions of Rho and Rho effectors came mostly from in vitro studies utilizing cultured cells, and their physiological roles in vivo were largely unknown. However, gene-targeting studies of Rho and its effectors have now unraveled their tissue- and cell-specific roles and provide deeper insight into the physiological function of Rho signaling in vivo. In this article, we briefly describe previous studies of the function of Rho and its effectors in vitro and then review and discuss recent studies on knockout mice of Rho and its effectors.

KEYWORDS:

Actin cytoskeleton; Citron; Knockout mouse; PKN; ROCK; Rho; Rho effectors; Rhophilin; Rhotekin; mDia

PMID:
24183240
DOI:
10.1016/j.ejcb.2013.09.002
[Indexed for MEDLINE]

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