Antiluteolytic mechanisms and the establishment of pregnancy in the pig.

A. Waclawik, A. Blitek, M. Kaczmarek, J. Kiewisz, A. Ziecik
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引用次数: 32

Abstract

Extended exposure of progesterone and conceptus estrogen influences the vascular compartment of the uterus and expression of many factors, such as prostaglandins (PGs), growth factors, extracellular matrix and adhesion molecules, cytokines and transcription factors. One of the supportive mechanisms by which the conceptus inhibits luteolysis is by changing PG synthesis in favor of luteoprotective PGE2. Alteration in PG synthesis may result from increased PGE synthase (mPGES-1) expression in the trophoblast and endometrium on days 10-13 of pregnancy with simultaneous down-regulation of PGF synthase (PGFS) and prostaglandin 9-ketoreductase (CBR1). Conceptus and endometrial, rather than luteal, synthesis of PGE2, is involved in the process of maternal recognition of pregnancy. However, complex (direct and indirect) actions of estrogen on the CL, including decreased luteal VEGF soluble receptor on day 12 of pregnancy, are important for luteal maintenance. Moreover, conceptus signals affect another lipid signaling component - lysophosphatidic acid receptor (LPA3), as well as HoxA10 and Wnt in the endometrium, to create the appropriate uterine environment for establishment of pregnancy and implantation.
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抗黄体溶解机制与猪妊娠的建立。
孕酮和孕雌激素的长期暴露影响子宫血管室和许多因子的表达,如前列腺素(pg)、生长因子、细胞外基质和粘附分子、细胞因子和转录因子。其中一个支持机制,通过概念抑制黄体溶解是通过改变PG合成有利于黄体保护PGE2。PG合成的改变可能是由于妊娠10-13天滋养细胞和子宫内膜中PGF合成酶(mPGES-1)表达增加,同时PGF合成酶(PGFS)和前列腺素9-酮还原酶(CBR1)下调。孕母和子宫内膜,而不是黄体,合成PGE2,参与母体对妊娠的识别过程。然而,雌激素对CL的复杂(直接和间接)作用,包括妊娠第12天黄体VEGF可溶性受体的降低,对黄体维持很重要。此外,妊娠信号影响另一种脂质信号成分溶血磷脂酸受体(LPA3)以及子宫内膜中的HoxA10和Wnt,为妊娠建立和着床创造适宜的子宫环境。
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Development of the pig placenta. Conceptus-uterus interactions in pigs: endometrial gene expression in response to estrogens and interferons from conceptuses. Temporal candidate gene expression patterns in the sow placenta during early gestation and the effect of maternal L-arginine supplementation. Genetic selection for lifetime reproductive performance. Global protein profiling of porcine cumulus cells in response to native oocyte secreted factors in vitro.
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