Adenosine 2A Receptor Activation Contributes to Ang II-Induced Aortic Remodeling by Promoting Macrophage Retention.

Abstract

The A2AR (adenosine 2A receptor) plays a crucial role in the pathophysiological process of cardiovascular diseases, yet its effect on aortic remodeling remains unclear. We observed elevated adenosine and A2AR levels following infusion of mice with Ang II (angiotensin II), suggesting a potential role for the adenosine-A2AR system in macrophage accumulation and subsequent aortic remodeling. The effects and mechanisms of A2AR on macrophage dynamics during aortic remodeling were further investigated using mice with macrophage knockout of A2AR and by transplantation of A2AR-/- bone marrow. We demonstrated that macrophage knockout of A2AR inhibited macrophage accumulation and subsequent aortic remodeling by inhibiting macrophage retention. This was shown to occur via promotion of macrophage emigration to the draining lymph node. These effects correlated with restoration of the expression and surface content of CCR7 (CC chemokine receptor 7). Consistently, A2AR-/- bone marrow transplantation relieved Ang II-induced aortic remodeling, macrophage retention, and CCR7 downregulation and internalization, all of which were rescued by A2AR+/+ bone marrow transplantation. In addition, CCR7 antibody treatment blocked all the protective effects observed in A2AR-cKO mice, including attenuation of aortic remodeling and decreased macrophage retention. In in vitro studies, A2AR activation induced by Ang II suppressed macrophage migration to CCL19 (CC-chemokine ligand) 19 through downregulation and internalization of CCR7. In summary, A2AR activation contributes to Ang II-induced macrophage retention and subsequent aortic remodeling by inhibiting migration of macrophages to the draining lymph node through regulating CCR7 expression and internalization.