Department of Animal Science, Oklahoma State University, Stillwater, OK 74078, USA.
Anim Reprod Sci. 2010 Dec;122(3-4):215-21. doi: 10.1016/j.anireprosci.2010.08.013. Epub 2010 Aug 20.
In pigs, administration of estrogen to gilts on Days 9 and 10 of pregnancy causes conceptus fragmentation and death between Days 15 and 18 of gestation. Conceptus degeneration is associated with breakdown of the microvilli surface glycocalyx on the lumenal epithelium (LE). We previously identified endometrial expression of inter-α-trypsin inhibitor (ITI) and hyaluronic acid (HA), which are key components of extracellular matrix (ECM), during the period of conceptus attachment to the uterine surface in the pig. Tumor necrosis factor-α-inducible protein-6 (TNFAIP6) serves as a linker for ECM expansion and is stimulated by prostaglandin E (PGE). We hypothesized that early estrogen administration alters the normal ECM components forming glycocalyx on the LE. Bred gilts (4 gilts/trt/day) were treated with either 5mg estradiol cypionate (E) or corn oil (CO) on Days 9 and 10 of gestation. The uterus was surgically removed on either Days 10, 12, 13, 15 and 17 of gestation and endometrial tissue snap frozen in liquid nitrogen. Endometrial tumor necrosis factor-α (TNF), TNFAIP6, interleukin 6 (IL6), and inter-α-trypsin inhibitor heavy chains (ITIH) were detected during early pregnancy thereby indicating all components for maintenance of the extracellular glycocalyx are present in the endometrium of pigs. However, only gene expression of ITIH2 was suppressed by E-treatment. TNFAIP6 protein was detected across all days of gestation but was not affected by E-treatment. The present study demonstrates that while the pig endometrium expresses key components of ECM only ITIH2 gene expression was altered by E-treatment. A decrease in ITIH2 could lead to the possible loss of the uterine glycocalyx leading to conceptus degeneration; however, other factors may be involved with the loss of glycocalyx during implantation in the pig following E-treatment.
在猪中,在妊娠第 9 天和第 10 天给小母猪施用雌激素会导致胚胎在妊娠第 15 天至第 18 天之间分裂和死亡。胚胎退化与腔上皮(LE)上微绒毛表面糖萼的破坏有关。我们之前在猪胚胎附着在子宫表面的时期发现了子宫内膜中表达的α-胰蛋白酶抑制剂(ITI)和透明质酸(HA),它们是细胞外基质(ECM)的关键组成部分。肿瘤坏死因子-α诱导蛋白-6(TNFAIP6)充当 ECM 扩展的连接物,并受前列腺素 E(PGE)刺激。我们假设早期雌激素给药会改变形成 LE 上糖萼的正常 ECM 成分。给繁殖小母猪(每天 4 头/处理)分别用 5mg 雌二醇环戊丙酸酯(E)或玉米油(CO)在妊娠第 9 天和第 10 天处理。在妊娠第 10、12、13、15 和 17 天通过手术取出子宫,并将子宫内膜组织立即在液氮中冷冻。在早期妊娠期间检测到子宫内膜肿瘤坏死因子-α(TNF)、TNFAIP6、白细胞介素 6(IL6)和α-胰蛋白酶抑制剂重链(ITIH),从而表明维持细胞外糖萼的所有成分都存在于猪的子宫内膜中。然而,只有 E 处理抑制了 ITIH2 的基因表达。TNFAIP6 蛋白在整个妊娠期间均有检测到,但不受 E 处理的影响。本研究表明,尽管猪子宫内膜表达 ECM 的关键成分,但只有 ITIH2 的基因表达被 E 处理改变。ITIH2 的减少可能导致子宫糖萼的可能丢失,导致胚胎退化;然而,在猪中,E 处理后植入过程中糖萼的丢失可能涉及其他因素。