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Автор Sah, Valerie P.
Автор Seasholtz, Tammy M.
Автор Sagi, Sarah A.
Автор Brown, Joan Heller
Дата выпуска 2000
dc.description Low molecular weight G proteins of the Rho subfamily are regulators of actin cytoskeletal organization. In contrast to the heterotrimeric G proteins, the small GTPases are not directly activated through ligand binding to G protein–coupled receptors (GPCRs). However, a subset of GPCRs, including those for lysophosphatidic acid and thrombin, induce stress fibers, focal adhesions, and cell rounding through Rho-dependent pathways. C3 exoenzyme has been a useful tool for demonstrating Rho involvement in these and other responses, including Ca<sup>2+</sup> sensitization of smooth muscle contraction, cell migration, transformation, and serum response element–mediated gene expression. Most of the GPCRs that induce Rho-dependent responses can activate Gq, but this is not a sufficient signal. Recent data demonstrate that Gα12/13 can induce Rho-dependent responses. Furthermore, Gα12/13 can bind and activate Rho-specific guanine nucleotide exchange factors, providing a mechanism by which GPCRs that couple to Gα12/13 could activate Rho and its downstream responses.
Формат application.pdf
Издатель Annual Reviews
Копирайт Annual Reviews
Название The Role of Rho in G Protein-Coupled Receptor Signal Transduction
DOI 10.1146/annurev.pharmtox.40.1.459
Print ISSN 0362-1642
Журнал Annual Review of Pharmacology and Toxicology
Том 40
Первая страница 459
Последняя страница 489
Аффилиация Sah, Valerie P.; Department of Pharmacology, University of California, San Diego, California, 92093– 0636; email: vtansah@ucsd.edu , tseasholtz@ucsd.edu , ssagi@ucsd.edu , and jhbrown@ucsd.edu

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