Parent J, Villeneuve C, Fortier M A
Unité de Recherche en Ontogénie et Reproduction, Centre Hospitalier Universitaire de Québec, Centre de Recherche en Biologie de la Reproduction, Ste-Foy, QC, Canada G1V 4G2.
Reproduction. 2003 Oct;126(4):539-47. doi: 10.1530/rep.0.1260539.
In ruminants, the production of prostaglandins by the endometrium is critical for recognition of pregnancy. In the absence of an embryonic signal, luteolytic pulses of PGF(2 alpha) are released by the uterus. In contrast, the presence of a viable conceptus reduces the production of PGF(2 alpha) relative to PGE(2) and prevents luteolysis through the release of trophoblastic interferon (IFN-tau). Initially, it was thought that epithelial and stromal endometrial cells were specialized in the production of a single type of prostaglandin. However, purified cell populations of both types of cell can produce PGF(2 alpha) and PGE(2); therefore, selective production of PGF(2 alpha) and PGE(2) must be regulated within each type of cell. Two distinct prostaglandin synthases, cyclooxygenase 1 and cyclooxygenase 2, are involved in prostaglandin production and each may catalyse the production of a different prostaglandin. This possibility was investigated in cultured epithelial cells from bovine endometrium. Cells were treated with oxytocin or arachidonic acid, and expression of cyclooxygenase 1 and cyclooxygenase 2 proteins was monitored over time and correlated with prostaglandin accumulation. Cells were also treated with increasing doses of inhibitors of cyclooxygenase 1 or cyclooxygenase 2 (non-steroidal anti-inflammatory drugs; NSAIDs) with or without arachidonic acid or oxytocin: flurbiprofen (0-50 micromol l(-1)) was used as a non-selective inhibitor; valeryl salicylate (0-500 micromol l(-1)) was used as a cyclooxygenase 1 inhibitor and NS-398 (0-1 micromol l(-1)) was used as a cyclooxygenase 2 inhibitor. After stimulation with arachidonic acid or oxytocin, prostaglandin production and expression of cyclooxygenase 2 protein were increased. All inhibitors were able to block basal and stimulated prostaglandin production. These results indicate that in endometrium most, if not all, prostaglandin production is probably processed through cyclooxygenase 2.
在反刍动物中,子宫内膜产生前列腺素对于识别妊娠至关重要。在没有胚胎信号的情况下,子宫会释放溶黄体脉冲的前列腺素F2α(PGF2α)。相反,存在存活的孕体相对于前列腺素E2(PGE2)会减少PGF2α的产生,并通过滋养层干扰素(IFN-τ)的释放来防止黄体溶解。最初,人们认为子宫内膜上皮细胞和基质细胞专门产生单一类型的前列腺素。然而,这两种类型细胞的纯化细胞群体都可以产生PGF2α和PGE2;因此,必须在每种类型的细胞内调节PGF2α和PGE2的选择性产生。两种不同的前列腺素合酶,即环氧化酶1和环氧化酶2,参与前列腺素的产生,并且每种酶可能催化产生不同的前列腺素。在来自牛子宫内膜的培养上皮细胞中研究了这种可能性。用催产素或花生四烯酸处理细胞,并随时间监测环氧化酶1和环氧化酶2蛋白的表达,并与前列腺素积累相关联。还用递增剂量的环氧化酶1或环氧化酶2抑制剂(非甾体抗炎药;NSAIDs)处理细胞,有或没有花生四烯酸或催产素:氟比洛芬(0-50微摩尔/升)用作非选择性抑制剂;戊酰水杨酸(0-500微摩尔/升)用作环氧化酶1抑制剂,NS-398(0-1微摩尔/升)用作环氧化酶2抑制剂。用花生四烯酸或催产素刺激后,前列腺素产生和环氧化酶2蛋白的表达增加。所有抑制剂都能够阻断基础和刺激的前列腺素产生。这些结果表明,在子宫内膜中,即使不是全部,大多数前列腺素的产生可能是通过环氧化酶2进行的。