Journal
JOURNAL OF LEUKOCYTE BIOLOGY
Volume 81, Issue 2, Pages 372-382Publisher
FEDERATION AMER SOC EXP BIOL
DOI: 10.1189/jlb.0706424
Keywords
CRTH2; DP; 15d-PGJ(2); inflammation and allergic disease
Categories
Funding
- Medical Research Council [G116/170] Funding Source: Medline
- MRC [G116/170] Funding Source: UKRI
- Medical Research Council [G0400503B, G116/170] Funding Source: researchfish
Ask authors/readers for more resources
Traditionally, PGD(2) has been considered to be a pro-inflammatory mediator, acting via classical PG receptors, such as the PGD(2) receptor (DP). PGD(2) is degraded rapidly in vitro and in vivo to a variety of metabolites, the majority of which were thought, until recently, to be physiologically inactive. Several inactive metabolites, particularly 15d-PGJ(2), have been shown to have wide-ranging effects on leukocytes and other cell types, however, and a potentially important anti-inflammatory role for PGD(2) has now been recognized, and the complexity of PGD(2) signaling is beginning to be elucidated. PGD(2) and its metabolites are biologically active over a broad concentration range, and, intriquingly, it appears that there are marked concentration-dependent variations in the consequences of signaling by these eicosanoids, which have the potential to exert pro- and anti-inflammatory effects. For example, the actions of PGD(2) can influence multiple stages in the life of the mature eosinophil, from causing its release from the bone marrow to inducing its recruitment and activation and, ultimately, regulating its apoptosis. This review is concerned with the diverse responses induced in leukocytes by PGD(2) and its metabolites and the signaling mechanisms which are thought to be responsible for them.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available