Blitek Agnieszka, Morawska-Pucinska Ewa, Szymanska Magdalena, Kiewisz Jolanta, Waclawik Agnieszka
Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, 10-748 Olsztyn, Poland.
J Reprod Dev. 2013 Dec 17;59(6):512-9. doi: 10.1262/jrd.2013-002. Epub 2013 Sep 15.
Transforming growth factor (TGF) β and its receptors are expressed at the conceptus-maternal interface during early pregnancy in the pig. The present studies were conducted to examine: (1) the effect of conceptus products on TGFβ1 mRNA expression and protein concentration in the porcine endometrium using in vivo and in vitro models, and (2) the effect of TGFβ1 on proliferation of porcine trophoblast cells in vitro. During in vivo experiments, gilts with one surgically detached uterine horn were slaughtered on days 11 or 14 of the estrous cycle and pregnancy. For in vitro studies, endometrial explants and luminal epithelial (LE) cells co-cultured with stromal (ST) cells were treated with conceptus-exposed medium (CEM). Moreover, porcine trophoblast cells were treated with TGFβ1, and the number of viable cells was measured. On day 11, the presence of conceptuses had no effect on TGFβ1 mRNA expression, but decreased the TGFβ1 protein concentration in the connected uterine horn compared with the detached uterine horn. In contrast to day 11, on day 14 after estrus, TGFβ1 mRNA expression and protein content in the endometrium collected from the gravid uterine horn were greater when compared with the contralateral uterine horn. The treatment of endometrial slices with CEM resulted in greater TGFβ1 mRNA expression and protein secretion. LE cells responded to CEM with an increased TGFβ1 mRNA level. Moreover, TGFβ1 stimulated the proliferation of day 14 trophoblast cells. In summary, porcine conceptuses may regulate TGFβ1 synthesis in the endometrium at the time of implantation. TGFβ1, in turn, may promote conceptus development by increasing the proliferation of trophoblast cells.
在猪的早期妊娠期间,转化生长因子(TGF)β及其受体在孕体 - 母体界面表达。本研究旨在检测:(1)使用体内和体外模型,孕体产物对猪子宫内膜中TGFβ1 mRNA表达和蛋白浓度的影响;(2)TGFβ1对猪滋养层细胞体外增殖的影响。在体内实验中,在发情周期和妊娠的第11天或第14天屠宰一侧子宫角经手术分离的后备母猪。对于体外研究,将与基质(ST)细胞共培养的子宫内膜外植体和腔上皮(LE)细胞用孕体暴露培养基(CEM)处理。此外,用TGFβ1处理猪滋养层细胞,并测量活细胞数量。在第11天,孕体的存在对TGFβ1 mRNA表达没有影响,但与分离的子宫角相比,连接子宫角中的TGFβ1蛋白浓度降低。与第11天相反,在发情后第14天,与对侧子宫角相比,从妊娠子宫角收集的子宫内膜中TGFβ1 mRNA表达和蛋白含量更高。用CEM处理子宫内膜切片导致TGFβ1 mRNA表达和蛋白分泌增加。LE细胞对CEM的反应是TGFβ1 mRNA水平升高。此外,TGFβ1刺激第14天滋养层细胞的增殖。总之,猪孕体可能在着床时调节子宫内膜中TGFβ1的合成。反过来,TGFβ1可能通过增加滋养层细胞的增殖来促进孕体发育。