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Circulation Research. 2006
Published online before print September 14, 2006, doi: 10.1161/01.RES.0000245187.08026.47
A more recent version of this article appeared on October 13, 2006
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Submitted on May 11, 2006
Revised on August 9, 2006
Accepted on August 31, 2006

Novel Mechanism of Endothelial Nitric Oxide Synthase Activation Mediated by Caveolae Internalization in Endothelial Cells

Nikolaos A. Maniatis ; Viktor Brovkovych ; Scott E. Allen ; Theresa A. John ; Ayesha N. Shajahan ; Chinnaswamy Tiruppathi ; Stephen M. Vogel ; Randal A. Skidgel ; Asrar B. Malik ; and Richard D. Minshall *

From the Departments of Pharmacology (N.A.M., V.B., S.E.A., T.A.J., A.N.S., C.T., S.M.V., R.A.S., A.B.M., R.D.M.) and Anesthesiology (R.D.M.) and the Center for Lung and Vascular Biology (V.B., C.T., S.M.V., R.A.S., A.B.M., R.D.M.), University of Illinois College of Medicine, Chicago.

* To whom correspondence should be addressed. E-mail: rminsh{at}uic.edu.

Caveolin-1, the caveolae scaffolding protein, binds to and negatively regulates eNOS activity. As caveolin-1 also regulates caveolae-mediated endocytosis after activation of the 60-kDa albumin-binding glycoprotein gp60 in endothelial cells, we addressed the possibility that endothelial NO synthase (eNOS)-dependent NO production was functionally coupled to caveolae internalization. We observed that gp60-induced activation of endocytosis increased NO production within 2 minutes and up to 20 minutes. NOS inhibitor NG-nitro-L-arginine (L-NNA) prevented the NO production. To determine the role of caveolae internalization in the mechanism of NO production, we expressed dominant-negative dynamin-2 mutant (K44A) or treated cells with methyl-{beta}-cyclodextrin. Both interventions inhibited caveolae-mediated endocytosis and NO generation induced by gp60. We determined the role of signaling via Src kinase in the observed coupling of endocytosis to eNOS activation. Src activation induced the phosphorylation of caveolin-1, Akt and eNOS, and promoted dissociation of eNOS from caveolin-1. Inhibitors of Src kinase and Akt also prevented NO production. In isolated perfused mouse lungs, gp60 activation induced NO-dependent vasodilation, whereas the response was attenuated in eNOS-/- or caveolin-1-/- lungs. Together, these results demonstrate a critical role of caveolae-mediated endocytosis in regulating eNOS activation in endothelial cells and thereby the NO-dependent vasomotor tone.


Key words: caveolin-1 • endocytosis • vasomotor tone • albumin • transcytosis


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