Nitric oxide synthase in innate and adaptive immunity: an update

被引:734
作者
Bogdan, Christian [1 ]
机构
[1] Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Mikrobiolog Inst, Klin Mikrobiol Immunol & Hyg, Wasserturmstr 3-5, D-91054 Erlangen, Germany
关键词
nitric oxide synthases (NOS1/nNOS; NOS2/iNOS; NOS3/eNOS); myeloid cells; microenvironment; antimicrobial activity; Th17; cells; B cells; MESENCHYMAL STEM-CELLS; ARGININE METABOLISM; HYDROGEN-SULFIDE; MOUSE MACROPHAGES; HEME OXYGENASE-1; S-NITROSYLATION; REACTIVE OXYGEN; MESSENGER-RNA; SIGNALING PATHWAYS; ALZHEIMERS-DISEASE;
D O I
10.1016/j.it.2015.01.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Thirty years after the discovery of its production by activated macrophages, our appreciation of the diverse roles of nitric oxide (NO) continues to grow. Recent findings have not only expanded our understanding of the mechanisms controlling the expression of NO synthases (NOS) in innate and adaptive immune cells, but have also revealed new functions and modes of action of NO in the control and escape of infectious pathogens, in T and B cell differentiation, and in tumor defense. I discuss these findings, in the context of a comprehensive overview of the various sources and multiple reaction partners of NO, and of the regulation of NOS2 by micromilieu factors, antisense RNAs, and 'unexpected' cytokines.
引用
收藏
页码:161 / 178
页数:18
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