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Prostanoids as Regulators of Innate and Adaptive Immunity
被引:85
|作者:
Hirata, Takako
[1
]
Narumiya, Shuh
[1
]
机构:
[1] Kyoto Univ, Grad Sch Med, Dept Pharmacol, Kyoto, Japan
来源:
ADVANCES IN IMMUNOLOGY, VOL 116
|
2012年
/
116卷
关键词:
MULTIPLE SIGNALING PATHWAYS;
MOUSE PROSTACYCLIN RECEPTOR;
PROSTAGLANDIN D-2 RECEPTOR;
DENDRITIC CELL-FUNCTION;
MICE LACKING;
ALLERGIC INFLAMMATION;
THROMBOXANE A(2);
FUNCTIONAL EXPRESSION;
CYTOKINE PRODUCTION;
INTERNATIONAL UNION;
D O I:
10.1016/B978-0-12-394300-2.00005-3
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Potent, oxygenated lipid molecules called prostanoids regulate a wide variety of physiological responses and pathological processes. Prostanoids are produced by various cell types and act on target cells through specific G protein-coupled receptors. Although prostanoids have historically been considered acute inflammation mediators, studies using specific receptor knockout mice indicate that prostanoids, in fact, regulate various aspects of both innate and adaptive immunity. Each prostanoid, depending on which receptor it acts on, exerts specific effects on immune cells such as macrophages, dendritic cells, and T and B lymphocytes, often in concert with microbial ligands and cytokines, to affect the strength, quality, and duration of immune responses. Prostanoids are also relevant to immunopathology, from inflammation to autoimmunity and cancer. Here, we review the role of prostanoids in regulating immunity, their involvement in immunopathology, and areas of insight that may lead to new therapeutic opportunities.
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页码:143 / 174
页数:32
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