Department of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, California 92037, USA.
Nat Rev Immunol. 2016 Mar;16(3):177-92. doi: 10.1038/nri.2016.4.
Cellular stress or apoptosis triggers the release of ATP, ADP and other nucleotides into the extracellular space. Extracellular nucleotides function as autocrine and paracrine signalling molecules by activating cell-surface P2 purinergic receptors that elicit pro-inflammatory immune responses. Over time, extracellular nucleotides are metabolized to adenosine, leading to reduced P2 signalling and increased signalling through anti-inflammatory adenosine (P1 purinergic) receptors. Here, we review how local purinergic signalling changes over time during tissue responses to injury or disease, and we discuss the potential of targeting purinergic signalling pathways for the immunotherapeutic treatment of ischaemia, organ transplantation, autoimmunity or cancer.
细胞应激或凋亡会导致 ATP、ADP 和其他核苷酸释放到细胞外空间。细胞外核苷酸通过激活细胞表面 P2 嘌呤能受体,作为自分泌和旁分泌信号分子发挥作用,从而引发促炎免疫反应。随着时间的推移,细胞外核苷酸被代谢为腺苷,导致 P2 信号传导减少,而通过抗炎腺苷(P1 嘌呤能)受体的信号传导增加。在这里,我们回顾了在组织对损伤或疾病的反应过程中,局部嘌呤能信号随时间的变化,并讨论了针对嘌呤能信号通路进行免疫治疗以治疗缺血、器官移植、自身免疫或癌症的潜力。