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Brief Reviews |
From the Department of Anesthesiology and Molecular Pharmacology and Experimental Therapeutics (Z.S.K.); Department of Medicine, Division of Cardiovascular Diseases (N.M.C.); Division of Nephrology (K.A.N.); and Molecular Medicine Program (Z.S.K., K.A.N.), Mayo Clinic, Rochester, Minn.
Correspondence to Zvonimir S. Katusic, MD, PhD, Department of Anesthesiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905. E-mail katusic.zvonimir{at}mayo.edu
Series Editor: Frank M. Faraci
ATVB In Focus
Endothelium: Signaling, Oxidative Stress, and Gene Expression
Previous Brief Reviews in this Series:
Wolfrum S. Jensen KS, Liao JK. Endothelium-dependent effects of statins. 2003;23:729736.
Frank PG, Woodman SE, Park DS, Lisanti MP. Caveolin, caveolae, and endothelial cell function. 2003;23:11611168.
During the past decade, the development of gene transfer technology provided a powerful and facile tool that afforded the genetic modification of vascular endothelial function. This development has coincided with molecular cloning and extensive accumulation of knowledge concerning the role of nitric oxide synthase isoforms in vascular homeostasis. Experimental evidence continues to accumulate that in vivo adenovirus-mediated gene transfer into the vessel wall is a very useful technique in studies designed to characterize function of a given gene or protein. In this review, we will use nitric oxide synthase gene transfer as a paradigm to illustrate how gene transfer technology can be used to address key issues in the vascular biology of endothelium.
Key Words: adenovirus endothelium superoxide anion protein kinase Akt vascular endothelial growth factor
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