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Blood, 15 February 2007, Vol. 109, No. 4, pp. 1495-1502.
Prepublished online as a Blood First Edition Paper on October 12, 2006; DOI 10.1182/blood-2006-06-029298.
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HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
Receptor activator of nuclear factor (NF) B ligand (RANKL) increases vascular permeability: impaired permeability and angiogenesis in eNOS-deficient mice
Jeong-Ki Min1,
Young-Lai Cho2,
Jae-Hoon Choi3,
Yonghak Kim1,
Jeong Hun Kim4,5,
Young Suk Yu4,5,
Jaerang Rho6,
Naoki Mochizuki7,
Young-Myeong Kim2,
Goo Taeg Oh3, and
Young-Guen Kwon1
1 Department of Biochemistry, College of Sciences, Yonsei University, Seoul, Republic of Korea;
2 Department of Molecular and Cellular Biochemistry, School of Medicine, Kangwon National University, Chunchon, Kangwon-Do, Republic of Korea;
4 Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea;
5 Seoul Artificial Eye Center, Clinical Research Institute, Seoul National University Hospital, Republic of Korea;
7 Department of Structural Analysis, National Cardiovascular Center Research Institute, Osaka, Japan;
6 Department of Microbiology, College of Natural Sciences, Chungnam National University, Daejeon, Republic of Korea;
3 Division of Molecular Life Science, Ewha Womans University, Seoul, Republic of Korea
Receptor activator of nuclear factor (NF) B ligand (RANKL) is emerging as an important regulator of vascular pathophysiology. Here, we demonstrate a novel role of RANKL as a vascular permeability factor and a critical role of endothelial nitric oxide synthase (eNOS) in RANKL-induced endothelial function. RANKL increased the vascular permeability and leukocyte infiltration in vivo and caused the breakdown of the blood-retinal barrier in wild-type mice but not in eNOS-deficient mice. In vitro, it increased endothelial permeability and reduced VE-cadherinfacilitated endothelial cell-cell junctions in a NO-dependent manner. RANKL also led to the activation of Akt and eNOS and to NO production in endothelial cells (ECs). These effects were suppressed by the inhibition of TRAF6, phosphoinositide 3'-kinase (PI3K), Akt, or NOS by genetic or pharmacologic means. Inhibition of the TRAF6-mediated NO pathway reduced EC migration and capillary-like tube formation in response to RANKL. Moreover, the effects of RANKL on ECs sprouting from the aorta, and neovessel formation in both the mouse Matrigel plug assay and corneal micropocket assay, were impaired in eNOS-deficient mice. These results demonstrate that RANKL promotes vascular permeability and angiogenesis by stimulating eNOS by a TRAF6-PI3K-Aktdependent mechanism. These properties may be relevant to the pathogenesis of angiogenesis-dependent and inflammatory vascular diseases.

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