Chhabra Preeti, Linden Joel, Lobo Peter, Okusa Mark Douglas, Brayman Kenneth Lewis
Department of Surgery, University of Virginia School of Medicine, P.O. Box 800709, Charlottesville, VA 22908-0709, USA.
Curr Diabetes Rev. 2012 Nov;8(6):419-33. doi: 10.2174/157339912803529878.
Activation of adenosine A2A receptors (A2AR) reduces inflammation by generally inhibiting the activation of pro-inflammatory cells, decreasing endothelial adhesion molecule expression and reducing the release of proinflammatory cytokine mediators. Numerous preclinical studies using selective A2AR agonists, antagonists, A2AR knockout as well as chimeric mice have suggested the therapeutic potential of A2AR agonists for the treatment of ischemia reperfusion injury (IRI) and autoimmune diseases. This review summarizes the immunosuppressive actions of A2AR agonists in murine IRI models of liver, kidney, heart, lung and CNS, and gives details on the cellular effects of A2AR activation in neutrophils, macrophages, dendritic cells, natural killer cells, NKT cells, T effector cells and CD4+CD25+FoxP3+ T regulatory cells. This is discussed in the context of cytokine mediators involved in inflammatory cascades. Whilst the role of adenosine receptor agonists in various models of autoimmune disease has been well-documented, very little information is available regarding the role of A2AR activation in type 1 diabetes mellitus (T1DM). An overview of the pathogenesis of T1DM as well as early islet graft rejection in the immediate peri-transplantation period offers insight regarding the use of A2AR agonists as a beneficial intervention in clinical islet transplantation, promoting islet graft survival, minimizing early islet loss and reducing the number of islets required for successful transplantation, thereby increasing the availability of this procedure to a greater number of recipients. In summary, the use of A2AR agonists as a clinical intervention in IRI and as an adjunct to clinical immunesuppressive regimen in islet transplantation is highlighted.
腺苷A2A受体(A2AR)的激活通常通过抑制促炎细胞的活化、降低内皮黏附分子表达以及减少促炎细胞因子介质的释放来减轻炎症。众多使用选择性A2AR激动剂、拮抗剂、A2AR基因敲除小鼠以及嵌合小鼠的临床前研究表明,A2AR激动剂在治疗缺血再灌注损伤(IRI)和自身免疫性疾病方面具有治疗潜力。本综述总结了A2AR激动剂在肝脏、肾脏、心脏、肺和中枢神经系统的小鼠IRI模型中的免疫抑制作用,并详细介绍了A2AR激活在中性粒细胞、巨噬细胞、树突状细胞、自然杀伤细胞、NKT细胞、T效应细胞和CD4+CD25+FoxP3+调节性T细胞中的细胞效应。这在参与炎症级联反应的细胞因子介质的背景下进行了讨论。虽然腺苷受体激动剂在各种自身免疫性疾病模型中的作用已有充分记录,但关于A2AR激活在1型糖尿病(T1DM)中的作用的信息却非常少。T1DM的发病机制以及移植后早期胰岛移植排斥反应的概述,为将A2AR激动剂作为临床胰岛移植的有益干预措施提供了见解,可促进胰岛移植存活、最大限度减少早期胰岛丢失并减少成功移植所需的胰岛数量,从而使更多受者能够接受该手术。总之,强调了将A2AR激动剂用作IRI的临床干预措施以及胰岛移植临床免疫抑制方案的辅助药物。