Institute of Liver Studies, King's College London School of Medicine at King's College Hospital, Denmark Hill, SE5 9RS, London, UK.
J Mol Med (Berl). 2013 Feb;91(2):165-72. doi: 10.1007/s00109-012-0991-z. Epub 2013 Jan 6.
When present in the extracellular environment, the nucleoside adenosine protects cells and tissues from excessive inflammation and immune-mediated damage while promoting healing processes. This role has been highlighted experimentally using distinct disease models, including those of colitis, diabetes, asthma, sepsis, and ischemic injury. Adenosine also suppresses immune responses, as in the tumor microenvironment, assisting immune evasion while promoting angiogenesis. The mechanisms involved in adenosine signaling are addressed elsewhere in this issue. Here, the authors specifically address the generation of adenosine from extracellular nucleotides. This process is catalyzed by a series of plasma membrane ectonucleotidases, with the focus in this article on members of the CD39, CD73, and CD38 families and on their role in inflammatory and neoplastic hematological diseases. Pharmacological modulation of adenosine generation by drugs that either have or modulate ectonucleotidase function might be exploited to treat these diverse conditions.
当存在于细胞外环境中时,核苷腺苷可保护细胞和组织免受过度炎症和免疫介导的损伤,同时促进愈合过程。这一作用在包括结肠炎、糖尿病、哮喘、败血症和缺血性损伤在内的不同疾病模型中得到了实验证实。腺苷还抑制免疫反应,例如在肿瘤微环境中,促进血管生成的同时协助免疫逃逸。腺苷信号转导的机制在本期杂志的其他地方有介绍。在这里,作者特别讨论了从细胞外核苷酸生成腺苷的过程。这个过程是由一系列质膜外核苷酸酶催化的,本文的重点是 CD39、CD73 和 CD38 家族的成员及其在炎症和肿瘤性血液病中的作用。通过药物调节腺苷的生成,这些药物要么具有外核苷酸酶功能,要么调节其功能,可能被用于治疗这些不同的疾病。