A2B adenosine receptors in immunity and inflammation

被引:187
|
作者
Hasko, Gyoergy [1 ,2 ]
Csoka, Balazs [1 ]
Nemeth, Zoltan H. [1 ,3 ]
Vizi, E. Sylvester [2 ]
Pacher, Pal [4 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Surg, Newark, NJ 07103 USA
[2] Hungarian Acad Sci, Inst Expt Med, Dept Pharmacol, H-1083 Budapest, Hungary
[3] Morristown Mem Hosp, Dept Surg, Morristown, NJ 07960 USA
[4] NIAAA, Sect Oxidat Stress Tissue Injury, Lab Physiol Studies, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
INTESTINAL EPITHELIAL-CELLS; HUMAN MAST-CELLS; INDUCED VASCULAR LEAK; SMOOTH-MUSCLE-CELLS; HIF-1-DEPENDENT REPRESSION; ECTO-5'-NUCLEOTIDASE CD73; PULMONARY INFLAMMATION; DEPENDENT INDUCTION; THERAPEUTIC TARGETS; MACROPHAGE FUNCTION;
D O I
10.1016/j.it.2009.04.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A(2B) adenosine receptors are increasingly recognized as important orchestrators of inflammation. A(2B) receptor activation promotes the inflammatory response of mast cells, epithelial cells, smooth muscle cells and fibroblasts, thereby contributing to the pathophysiology of asthma and colitis. A(2B) receptor stimulation limits endothelial cell inflammatory responses and permeability and suppresses macrophage activation thereby preventing tissue injury after episodes of hypoxia and ischemia. A(2B) receptor stimulation also promotes the production of angiogenic cytokines by endothelial cells, mast cells and dendritic cells, aiding granuloma tissue formation and inflammatory resolution, but can also contribute to tumor growth. A(2B) receptors are, thus, potentially important pharmacological targets in treating immune system dysfunction and inflammation.
引用
收藏
页码:263 / 270
页数:8
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