Kliewer S A, Lenhard J M, Willson T M, Patel I, Morris D C, Lehmann J M
Department of Cell Biology, Glaxo Research Institute, Research Triangle Park, North Carolina 27709, USA.
Cell. 1995 Dec 1;83(5):813-9. doi: 10.1016/0092-8674(95)90194-9.
Prostaglandins (PGs) of the J2 series form in vivo and exert effects on a variety of biological processes. While most of PGs mediate their effects through G protein-coupled receptors, the mechanism of action for the J2 series of PGs remains unclear. Here, we report the PGJ2 and its derivatives are efficacious activators of peroxisome proliferator-activated receptors alpha and gamma (PPAR alpha and PPAR gamma, respectively), orphan nuclear receptors implicated in lipid homeostasis and adipocyte differentiation. The PGJ2 metabolite 15-deoxy-delta 12,14-PGJ2 binds directly to PPAR gamma and promotes efficient differentiation of C3H10T1/2 fibroblasts to adipocytes. These data provide strong evidence that a fatty acid metabolite can function as an adipogenic agent through direct interactions with PPAR gamma and furthermore, suggest a novel mechanism of action for PGs of the J2 series.
J2系列前列腺素(PGs)在体内形成,并对多种生物学过程产生影响。虽然大多数PGs通过G蛋白偶联受体介导其作用,但J2系列PGs的作用机制仍不清楚。在此,我们报告PGJ2及其衍生物是过氧化物酶体增殖物激活受体α和γ(分别为PPARα和PPARγ)的有效激活剂,这两种孤儿核受体与脂质稳态和脂肪细胞分化有关。PGJ2代谢产物15-脱氧-Δ12,14-PGJ2直接与PPARγ结合,并促进C3H10T1/2成纤维细胞高效分化为脂肪细胞。这些数据提供了强有力的证据,证明一种脂肪酸代谢产物可通过与PPARγ的直接相互作用发挥成脂剂的功能,此外,还提示了J2系列PGs的一种新作用机制。