Adenosine binding to adenylyl cyclase stimulatory (A2-type) adenosine receptors (ARs) induces coronary vasodilatation, inhibits human aortic vascular smooth muscle cell proliferation, and affects arterial wall matrix production, all of which are important components of atherosclerosis/restenosis. The role of the low affinity A2bARs in regulating vascular pathology in vivo had not been examined prior to our study. To further address this, we generated the first A2bAR-knockout (KO)/reporter gene-knock-in mouse model and showed reported gene expression primarily in VSMC and macrophages, in accordance with the endogenous profile in control mice. Augmentation of proinflammatory cytokines, such as tumor necrosis factor-1 (TNF-1), is the underlying mechanism for an observed upregulation of leukocyte adhesion in the vasculature of these A2bAR KO mice, as compared with age-, sex-, and strain-matched control mice. On the other hand, the A2bAR gene receptor, itself, is induced by TNF-1, suggesting a regulatory loop. A2bAR KO mice display greater lesion formation after guidewire-induced femoral artery injury. This occurs in association with the upregulation of CXCR4, a protein known to promote mobilization of progenitors and inflammatory cells to the vessel by interaction with its ligand stromal cell-derived factor-1 (SDF-1). Furthermore, bone marrow (BM) transplantation experiments indicate that the inflammatory response and vascular lesion formation are significantly regulated by BM-derived A2bARs. Building upon these novel findings, we hypothesize that A2bAR-mediated signaling regulates the expression of CXRC4 and, hence, plays a vital role in vascular lesion formation. It is our contention that macrophage A2bARs, via their ability to control the level of inflammatory cytokines, are capable of significantly protecting against vascular pathology on their own, consistent with the BM transplantation experiments. Finally, identifying mechanisms of A2bAR gene regulation by TNF-1 should lead the way for the development of strategies for controlling vascular dysfunction during inflammation.
Three specific aims of research are proposed:
Aim 1. To examine the direct participation of BM cells and/or their signals in mediating effects of the A2bAR on lesion formation during vascular injury and atherosclerosis, and to study related mechanisms, with a focus on the contribution of macrophage A2bARs.
Aim 2. To elucidate the mechanism of control of the CXCR4/SDF-1 axis by the A2bAR.
Aim 3. To study the mechanism of A2bAR gene activation by TNF-1 in primary cultures and in vivo. Taken together, our proposed investigations should shed new light on the role of A2bARs in the pathogenesis of vascular dysfunction, and could focus attention on A2bAR activation as a therapeutic target.
Atherosclerosis is a leading cause of vascular disease in the Western world. Our research proposal builds upon novel findings, including the identification of the A2b adenosine receptor as protective against atherosclerosis/restenosis. The mechanisms leading to this protection and the control of expression of this receptor gene are the focus of research in this proposal.
|Sun, Ying; Hu, Wenbao; Yu, Xiaojie et al. (2016) Actinin-1 binds to the C-terminus of A2B adenosine receptor (A2BAR) and enhances A2BAR cell-surface expression. Biochem J 473:2179-86|
|Jing, Lili; Tamplin, Owen J; Chen, Michael J et al. (2015) Adenosine signaling promotes hematopoietic stem and progenitor cell emergence. J Exp Med 212:649-63|
|Coughlan, Karen S; Mitchem, Mollie R; Hogg, Marion C et al. (2015) ""Preconditioning"" with latrepirdine, an adenosine 5'-monophosphate-activated protein kinase activator, delays amyotrophic lateral sclerosis progression in SOD1(G93A) mice. Neurobiol Aging 36:1140-50|
|Eisenstein, Anna; Patterson, Shenia; Ravid, Katya (2015) The Many Faces of the A2b Adenosine Receptor in Cardiovascular and Metabolic Diseases. J Cell Physiol 230:2891-7|
|Eisenstein, Anna; Carroll, Shannon H; Johnston-Cox, Hillary et al. (2014) An adenosine receptor-Krüppel-like factor 4 protein axis inhibits adipogenesis. J Biol Chem 289:21071-81|
|Eisenstein, Anna; Ravid, Katya (2014) G protein-coupled receptors and adipogenesis: a focus on adenosine receptors. J Cell Physiol 229:414-21|
|Johnston-Cox, Hillary; Eisenstein, Anna S; Koupenova, Milka et al. (2014) The macrophage A2B adenosine receptor regulates tissue insulin sensitivity. PLoS One 9:e98775|
|Koupenova, Milka; Ravid, Katya (2013) Adenosine, adenosine receptors and their role in glucose homeostasis and lipid metabolism. J Cell Physiol :|
|Koupenova, Milka; Johnston-Cox, Hillary; Ravid, Katya (2012) Regulation of atherosclerosis and associated risk factors by adenosine and adenosine receptors. Curr Atheroscler Rep 14:460-8|
|Koupenova, Milka; Johnston-Cox, Hillary; Vezeridis, Alexander et al. (2012) A2b adenosine receptor regulates hyperlipidemia and atherosclerosis. Circulation 125:354-63|
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