Prostaglandin J2 Family and the Cardiovascular System

受体 血管平滑肌 血管内皮生长因子B 细胞生物学 前列腺素 脂质运载蛋白 前列腺素D2 医学 内分泌学 药理学 内科学 生物 癌症研究 血管内皮生长因子A 血管内皮生长因子 平滑肌 血管内皮生长因子受体
作者
Toshiyuki Sasaguri,Yoshikazu Miwa
出处
期刊:Current Vascular Pharmacology [Bentham Science Publishers]
卷期号:2 (2): 103-114 被引量:19
标识
DOI:10.2174/1570161043476384
摘要

Prostaglandins (PGs) of the J2 family including PGJ2, delta12-PGJ2, and 15-deoxy-delta12,14-PGJ2 (15d-PGJ2) are naturally occurring metabolites of PGD2. Among them, 15d-PGJ2 is a powerful ligand for the peroxisome proliferator-activated receptor-gamma (PPARgamma). 15d-PGJ2 and synthetic PPARgamma ligands have been reported to exert several effects on vascular cells, such as anti-proliferative, differentiation-inducing, anti-apoptotic, and anti-inflammatory effects, most of which seem to be atheroprotective, although PPARgamma-independent mechanisms may be involved. Vascular endothelial cells, intimal smooth muscle cells, and cardiomyocytes express lipocalin-type PGD synthase (L-PGDS) in vivo, which catalyzes the isomeric conversion of PGH2 to PGD2. L-PGDS expression in endothelial cells is stimulated by laminar fluid shear stress. PGD2 and 15d-PGJ2 are detected in the culture medium of endothelial cells exposed to shear stress. Serum and urinary levels of L-PGDS increase in diseases with vascular injuries, such as hypertension and diabetes. Based on these findings, we hypothesize that PGs of the J2 series are physiological substances produced in the vascular wall to protect vascular cells from injurious stimuli and to repress inflammatory reactions. If this hypothesis is correct, PGJ2 family members or other similar substances may provide novel preventive and therapeutic strategies for the treatment of vascular diseases.
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