Centre for Molecular Medicine Norway, Nordic EMBL Partnership and Biotechnology Centre, University of Oslo, Oslo, Norway.
Br J Pharmacol. 2012 May;166(2):411-9. doi: 10.1111/j.1476-5381.2011.01800.x.
Cyclic AMP is the intracellular second messenger for a variety of immunoregulatory inflammatory mediators such as prostaglandin E2, adenosine and histamine that signal to effector T cells from monocytes, macrophages and regulatory T cells. Protein kinase A (PKA) type I localizes to lipid rafts in effector T cells during T cell activation and directly modulates proximal signal events including phosphorylation of C-terminal Src kinase (Csk), which initiates a negative signal pathway that fine-tunes the T cell activation process. The PKA-Csk immunoregulatory pathway is scaffolded by the A kinase anchoring protein ezrin, the Csk binding protein phosphoprotein associated with glycosphingolipid-enriched membrane microdomains and the linker protein ezrin/radixin/moesin binding protein of 50 kDa. This pathway is hyperactivated in chronic infections with an inflammatory component such as HIV, other immunodeficiencies and around solid tumours as a consequence of local inflammation leading to inhibition of anti-tumour immunity. LINKED ARTICLES This article is part of a themed section on Novel cAMP Signalling Paradigms. To view the other articles in this section visit http://dx.doi.org/10.1111/bph.2012.166.issue-2.
环磷酸腺苷是多种免疫调节炎症介质的细胞内第二信使,如前列腺素 E2、腺苷和组胺,它们向单核细胞、巨噬细胞和调节性 T 细胞中的效应 T 细胞发出信号。蛋白激酶 A(PKA)I 型在 T 细胞激活过程中定位于效应 T 细胞的脂筏中,并直接调节包括 C 末端Src 激酶(Csk)磷酸化在内的近端信号事件,该激酶启动负信号通路,微调 T 细胞激活过程。PKA-Csk 免疫调节途径由 AKAP ezrin、与富含糖脂的膜微区结合的 Csk 结合蛋白磷酸蛋白以及 ezrin/radixin/moesin 结合蛋白 50kDa 的链接蛋白支架构成。在具有炎症成分的慢性感染(如 HIV、其他免疫缺陷和实体瘤周围)中,该途径被过度激活,这是由于局部炎症导致抗肿瘤免疫抑制。
相关文章 本文是关于新型 cAMP 信号范式专题的一部分。要查看本节中的其他文章,请访问 http://dx.doi.org/10.1111/bph.2012.166.issue-2。