期刊
THESCIENTIFICWORLDJOURNAL
卷 7, 期 -, 页码 1165-1181出版社
HINDAWI LTD
DOI: 10.1100/tsw.2007.224
关键词
glucocorticoids; apoptosis; inflammation; macrophage phagocytosis
资金
- Medical Research Council [G0601481] Funding Source: Medline
- Wellcome Trust Funding Source: Medline
- MRC [G0601481] Funding Source: UKRI
The glucocorticoid (GC) drugs are one of the most commonly prescribed and effective anti-inflammatory agents used for the treatment of many inflammatory disorders through their ability to attenuate phlogistic responses. The glucocorticoid receptor (GCR) primarily mediates GC actions via activation or repression of gene expression. GCs directly induce the expression of proteins displaying anti-inflammatory activities. However, the likely predominant effect of GCs is the repression of multiple inflammatory genes that invariably are overexpressed during nonresolving chronic inflammation. Although most GC actions are mediated through regulation of transcription, rapid nongenomic actions have also been reported. In addition, GCs modulate inflammatory cell survival, inducing apoptosis in immature thymocytes and eosinophils, while delaying constitutive neutrophil apoptosis. Importantly, GCs promote noninflammatory phagocytosis of apoptotic cell targets, a process important for the successful resolution of inflammation. Here, the effects and mechanisms of action of GC on inflammatory cell apoptosis and phagocytosis will be discussed.
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