期刊
VASCULAR PHARMACOLOGY
卷 74, 期 -, 页码 60-72出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.vph.2015.10.003
关键词
RhoGEF; Rho GTPases; Rac; Cdc42; VEGF; Endothelial cell cytoskeleton; Tumor angiogenesis
资金
- Consejo Nacional de Ciencia y Tecnologia (CONACyT) [152434, 79429]
- University of California Institute for Mexico and the United States, UC-Mexus-Conacyt collaborative grant
- CONACyT fellowship
Rho guanine nucleotide exchange factors (RhoGEFs) integrate cell signaling inputs into morphological and functional responses. However, little is known about the endothelial repertoire of RhoGEFs and their regulation. Thus, we assessed the expression of 81 RhoGEFs (70 homologous to Db1 and 11 of the DOCK family) in endothelial cells. Further, in the case of DH-RhoGEFs, we also determined their responses to VEGF exposure in vitro and in the context of tumors. A phylogenetic analysis revealed the existence of four groups of DH-RhoGEFs and two of the DOCK family. Among them, we found that the most abundant endothelial RhoGEFs were: Tuba, FGD5, Farp1, ARHGEF17, TRIO, P-Rex1, ARHGEF15, ARHGEF11, ABR, Farp2, ARHGEF40, ALS, DOCK1, DOCK7 and DOCK6. Expression of RASGRF2 and PREX2 increased significantly in response to VEGF, but most other RhoGEFs were unaffected. Interestingly murine endothelial cells isolated from tumors showed that all four phylogenetic subgroups of DH-RhoGEFs were altered when compared to non-tumor endothelial cells. In summary, our results provide a detailed assessment of RhoGEFs expression profiles in the endothelium and set the basis to systematically address their regulation in vascular signaling. (C) 2015 Elsevier Inc. All rights reserved.
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