Regulation of Macrophage Function by Adenosine

被引:180
作者
Hasko, Gyorgy [1 ,2 ]
Pacher, Pal [3 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Surg, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Ctr Immun & Inflammat, Newark, NJ 07103 USA
[3] NIAAA, Lab Physiol Studies, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
cytokines; G proteins; immune system; immunosuppressive therapy; macrophages; ENDOTHELIAL GROWTH-FACTOR; NECROSIS-FACTOR-ALPHA; ALTERNATIVELY ACTIVATED MACROPHAGES; SYNERGISTIC UP-REGULATION; A(2A) RECEPTOR AGONISTS; TNF-ALPHA; MURINE MACROPHAGES; A2A RECEPTOR; EXPRESSION; A(2B);
D O I
10.1161/ATVBAHA.111.226852
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Following its release into the extracellular space in response to metabolic disturbances, the endogenous nucleoside adenosine exerts a range of immunomodulatory effects and cells of the mononuclear phagocyte system are among its major targets. Adenosine governs mononuclear phagocyte functions via 4 G-protein-coupled cell membrane receptors, which are denoted A(1), A(2A), A(2B), and A(3) receptors. Adenosine promotes osteoclast differentiation via A(1) receptors and alters monocyte to dendritic cell differentiation through A(2B) receptors. Adenosine downregulates classical macrophage activation mainly through A(2A) receptors. In contrast A(2B) receptor activation upregulates alternative macrophage activation. Adenosine promotes angiogenesis, which is mediated by inducing the production of vascular endothelial growth factor by mononuclear phagocytes through A(2A), A(2B), and A(3) receptors. By regulating mononuclear phagocyte function adenosine dictates the course of inflammatory and vascular diseases and cancer. (Arterioscler Thromb Vasc Biol. 2012;32:865-869.)
引用
收藏
页码:865 / 869
页数:5
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