There is compelling evidence that the G-protein coupled receptor APJ and its cognate peptide ligand apelin constitute a signaling pathway employed by the endothelial cell to regulate numerous aspects of cardiovascular function and response to disease. 1) In the adult vasculature, circulating apelin binding APJ on endothelial cells decreases blood pressure in a nitric oxide-dependent fashion. 2) Endothelial cells in culture are stimulated by apelin to migrate and divide, and this stimulation is mediated in part by nitric oxide. 3) The differential expression of apelin mRNA levels in response to laminar shear stress, hypoxia, oxidative stress, and vascular disease suggests that apelin is involved in atherosclerosis or the vessel response to disease. 4) In the heart, apelin produced by coronary endothelial cells provides one of the most potent inotropic signals yet characterized for myocardial cells. We hypothesize that the apelin-APJ signaling pathway provides the endothelial cell a highly regulated mechanism for monitoring and adjusting cardiovascular homeostatic mechanisms, including a key adaptive response to injury in the vessel wall. Experiments proposed in this application will investigate salient features of the apelin-APJ signaling pathway in the vasculature, and how it interacts with the nitric oxide and angiotensin pathways to modulate disease processes. Primarily, experiments will focus on mouse genetic models designed to express no apelin (knockout mice) or express increased levels of apelin (human BAG transgenic mice) as well as tissue-restricted APJ knockout mice, and wild type mice with pharmacological modulation of signaling. The physiological role of pathway activation will be evaluated with three approaches. Comprehensive studies conducted on explanted vessels will directly examine the effects of apelin-APJ signaling on vascular tone and investigate underlying mechanisms for these effects; conductance catheter measurements will evaluate the in vivo inotropic effects of apelin and allow the discrimination of cardiac versus vascular effects in responses to manipulation of apelin expression level. The role of apelin and APJ in vascular pathophysiology will be evaluated with the apoE knockout model of atherosclerosis, and the carotid artery ligation model of vascular remodeling. In vivo studies will be complemented with targeted in vitro studies designed to elucidate fundamental cellular functions that are initiated in endothelial cells by this pathway. ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL077676-03
Application #
7234785
Study Section
Vascular Cell and Molecular Biology Study Section (VCMB)
Program Officer
Goldman, Stephen
Project Start
2005-06-01
Project End
2009-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
3
Fiscal Year
2007
Total Cost
$372,183
Indirect Cost
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Yue, Patrick; Jin, Hong; Xu, Shiming et al. (2011) Apelin decreases lipolysis via G(q), G(i), and AMPK-Dependent Mechanisms. Endocrinology 152:59-68
Terashima, Masahiro; Ehara, Shoichi; Yang, Eugene et al. (2011) In vivo bioluminescence imaging of inducible nitric oxide synthase gene expression in vascular inflammation. Mol Imaging Biol 13:1061-6
Leeper, Nicholas J; Raiesdana, Azad; Kojima, Yoko et al. (2011) MicroRNA-26a is a novel regulator of vascular smooth muscle cell function. J Cell Physiol 226:1035-43
Chandra, Suparna M; Razavi, Hedi; Kim, Jongmin et al. (2011) Disruption of the apelin-APJ system worsens hypoxia-induced pulmonary hypertension. Arterioscler Thromb Vasc Biol 31:814-20
Yue, Patrick; Jin, Hong; Aillaud, Marissa et al. (2010) Apelin is necessary for the maintenance of insulin sensitivity. Am J Physiol Endocrinol Metab 298:E59-67
Cangara, Husni M; Ishida, Tatsuro; Hara, Tetsuya et al. (2010) Role of endothelial cell-selective adhesion molecule in hematogeneous metastasis. Microvasc Res 80:133-41
Kojima, Yoko; Kundu, Ramendra K; Cox, Christopher M et al. (2010) Upregulation of the apelin-APJ pathway promotes neointima formation in the carotid ligation model in mouse. Cardiovasc Res 87:156-65
Leeper, Nicholas J; Tedesco, Maureen M; Kojima, Yoko et al. (2009) Apelin prevents aortic aneurysm formation by inhibiting macrophage inflammation. Am J Physiol Heart Circ Physiol 296:H1329-35

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