The smooth muscle-selective RhoGAP GRAF3 is a critical regulator of vascular tone and hypertension

• DOI: 10.1038/ncomms3910
• Publication Date: 2013-12-13T10:48:15Z
• Authors: Xue Bai; Kaitlin C. Lenhart; Kim E. Bird; Alisa A. Suen; Mauricio Rojas; Masao Kakoki; Feng Li; Oliver Smithies; Christopher P. Mack; Joan M. Taylor
• Keywords: Homeostasis

Although hypertension is a worldwide health issue, an incomplete understanding of its etiology has hindered our ability to treat this complex disease. Here we identify arhgap42 (also known as GRAF3) as a Rho-specific GAP expressed specifically in smooth muscle cells in mice and humans. We show that GRAF3-deficient mice exhibit significant hypertension and increased pressor responses to angiotensin II and endothelin-1; these effects are prevented by treatment with the Rho-kinase inhibitor, Y-27632. RhoA activity and myosin light chain phosphorylation are elevated in GRAF3-depleted smooth muscle cells in vitro and in vivo, and isolated vessel segments from GRAF3-deficient mice show increased contractility. Taken together our data indicate that GRAF3-mediated inhibition of RhoA activity in vascular smooth muscle cells is necessary for maintaining normal blood pressure homeostasis. Moreover, these findings provide a potential mechanism for a hypertensive locus recently identified within arhgap42 and provide a foundation for the future development of innovative hypertension therapies.