Sheldrick E Linda R, Derecka Kamila, Marshall Elaine, Chin Evonne C, Hodges Louise, Wathes D Claire, Abayasekara D Robert E, Flint Anthony P F
Division of Animal Physiology, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, UK.
Biochem J. 2007 Aug 15;406(1):175-83. doi: 10.1042/BJ20070089.
Arachidonic acid is a potential paracrine agent released by the uterine endometrial epithelium to induce PTGS2 [PG (prostaglandin)-endoperoxide synthase 2] in the stroma. In the present study, bovine endometrial stromal cells were used to determine whether PTGS2 is induced by arachidonic acid in stromal cells, and to investigate the potential role of PPARs (peroxisome-proliferator-activated receptors) in this effect. Arachidonic acid increased PTGS2 levels up to 7.5-fold within 6 h. The cells expressed PPARalpha and PPARdelta (also known as PPARbeta) (but not PPARgamma). PTGS2 protein level was increased by PPAR agonists, including polyunsaturated fatty acids, synthetic PPAR ligands, PGA1 and NSAIDs (non-steroidal anti-inflammatory drugs) with a time course resembling that of arachidonic acid. Use of agonists and antagonists indicated PPARalpha (but not PPARdelta or PPARgamma) was responsible for PTGS2 induction. PTGS2 induction by arachidonic acid did not require PG synthesis. PTGS2 levels were increased by the PKC (protein kinase C) activators 4beta-PMA and PGF(2alpha), and the effects of arachidonic acid, NSAIDs, synthetic PPAR ligands and 4beta-PMA were blocked by PKC inhibitors. This is consistent with PPAR phosphorylation by PKC. Induction of PTGS2 protein by 4beta-PMA in the absence of a PPAR ligand was decreased by the NF-kappaB (nuclear factor kappaB) inhibitors MG132 and parthenolide, suggesting that PKC acted through NF-kappaB in addition to PPAR phosphorylation. Use of NF-kappaB inhibitors allowed the action of arachidonic acid as a PPAR agonist to be dissociated from an effect through PKC. The results are consistent with the hypothesis that arachidonic acid acts via PPARalpha to increase PTGS2 levels in bovine endometrial stromal cells.
花生四烯酸是一种由子宫内膜上皮释放的潜在旁分泌因子,可诱导基质中的PTGS2[PG(前列腺素)-内过氧化物合酶2]。在本研究中,使用牛子宫内膜基质细胞来确定PTGS2是否由基质细胞中的花生四烯酸诱导,并研究PPARs(过氧化物酶体增殖物激活受体)在这种作用中的潜在作用。花生四烯酸在6小时内使PTGS2水平增加高达7.5倍。细胞表达PPARα和PPARδ(也称为PPARβ)(但不表达PPARγ)。PPAR激动剂,包括多不饱和脂肪酸、合成PPAR配体、PGA1和非甾体抗炎药(NSAIDs),可使PTGS2蛋白水平升高,其时间进程与花生四烯酸相似。激动剂和拮抗剂的使用表明,PTGS2的诱导是由PPARα(而非PPARδ或PPARγ)介导的。花生四烯酸诱导PTGS2不需要PG合成。蛋白激酶C(PKC)激活剂4β-PMA和PGF(2α)可使PTGS2水平升高,PKC抑制剂可阻断花生四烯酸、NSAIDs、合成PPAR配体和4β-PMA的作用。这与PKC对PPAR的磷酸化作用一致。在没有PPAR配体的情况下,4β-PMA诱导的PTGS2蛋白表达可被核因子κB(NF-κB)抑制剂MG132和小白菊内酯降低,这表明PKC除了使PPAR磷酸化外,还通过NF-κB发挥作用。NF-κB抑制剂的使用使花生四烯酸作为PPAR激动剂的作用与通过PKC的作用得以分离。这些结果与花生四烯酸通过PPARα作用增加牛子宫内膜基质细胞中PTGS2水平的假说一致。