IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY
Haidee Tinning, Elton J R Vasconcelos, Dapeng Wang, Niamh Forde
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引用次数: 0

摘要

早期胚胎丢失影响所有哺乳动物物种,包括人类和牛等重要的农业产粮哺乳动物。发育中的胚胎(胚胎和胚胎外膜)会分泌改变子宫内膜的因子,这些因子对早期妊娠过程(如母体识别妊娠(MRP)和提高子宫对植入的接受能力)至关重要。例如,有能力的牛受孕期会分泌 IFNT 以启动 MRP。牛的受孕体在妊娠母体识别(MRP)时还会分泌其他蛋白,包括在胎盘哺乳动物中高度保守的 CAPG 和 PDI。我们以前的研究表明,这些蛋白可作用于子宫内膜,调节不同植入策略物种(人类和牛)的接受能力、胚胎发育和植入。我们假设,开发一种新型三维牛子宫内膜芯片系统将有助于我们更好地了解受体衍生因子在改变子宫内膜和/或超微基质分泌中的作用。与传统的二维子宫内膜细胞培养相比,我们在此开发了一种三维牛子宫内膜芯片系统,该系统包括基质细胞和上皮细胞培养,培养基流能更好地模拟体内子宫内膜和受孕因子暴露。我们已经证明,孕卵衍生蛋白 CAPG 和 PDI 可调节子宫内膜转录组和分泌反应,从而促进与早孕相关的通路并改变超低密度脂蛋白的组成。这项工作突出表明,我们亟需更强大的、类似于活体的培养系统来研究子宫内膜与孕囊在体外的相互作用,从而进一步研究孕囊衍生因子对妊娠成功的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A bovine 3D endometrium-on-a-chip reveals the role of conceptus-derived factors CAPG and PDI in conceptus-endometrial communication.

Early embryo loss affects all mammalian species, including humans and agriculturally important food-producing mammals such as cattle. The developing conceptus (embryo and extra-embryonic membranes) secretes factors which modify the endometrium and can be critical for early pregnancy processes such maternal recognition of pregnancy (MRP) and enhancing uterine receptivity to implantation. For example, a competent bovine conceptus secretes IFNT to initiate MRP. The bovine conceptus also secretes other proteins at the time of MRP, including CAPG and PDI, which are highly conserved among placental mammals. We have previously shown that these proteins act upon the endometrium to modulate receptivity, embryo development, and implantation in species with different implantation strategies (humans and cattle). We hypothesise that developing a novel 3D bovine endometrium on a chip system will enhance our understanding of the role of conceptus-derived factors in altering the endometrium and/or ULF secretion. Here we have developed a 3D bovine endometrium on a chip system, comprising both stromal and epithelial cell culture combined with culture medium flow better mimics the in vivo endometrium and exposure to conceptus-derived factors than conventional 2D endometrial cell culture. We have demonstrated that the conceptus-derived proteins CAPG and PDI modulate the endometrial transcriptome and secretory response to promote pathways associated with early pregnancy and alter ULF composition. This work highlights the critical need for more robust and in vivo-like culture systems to study endometrial-conceptus interactions in vitro to further investigate the role of conceptus derived factors for pregnancy success.

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来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
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