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基质金属蛋白酶可改善小鼠滋养层细胞的侵袭能力和妊娠潜能。

Matrix metalloproteinases improves trophoblast invasion and pregnancy potential in mice.

机构信息

Department of Animal Science, Division of Applied Life Science (BK21 Plus), Gyeongsang National University, Jinju, 52828, Gyeongnam Province, Republic of Korea.

Department of Theriogenology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, 44519, Egypt.

出版信息

Theriogenology. 2020 Jul 15;151:144-150. doi: 10.1016/j.theriogenology.2020.02.002. Epub 2020 Feb 5.

DOI:10.1016/j.theriogenology.2020.02.002
PMID:32344273
Abstract

Successful implantation is closely linked to the expression of MMP-2 and MMP-9, which greatly influence the ability of an embryo to degrade the basement membrane of the uterine epithelium, mainly composed of type IV collagen, and invade the uterine stroma. The objective of this study was to determine the effect of MMP-2 and MMP-9 co-transfer with embryos on reproductive performance in mice. Using invasion assay, we tested the effect of MMP-2 and MMP-9 for their ability to support trophoblastic invasion in vitro. We performed co-transfer of MMP-2 and MMP-9 with mouse embryos to 2.5 days post-coitum (dpc) pseudo-pregnant uteri using nonsurgical embryo transfer (NSET) technique and evaluated the pregnancy outcomes. Uterine tissue samples were collected to determine collagen content by Masson's trichrome staining. Our results showed that in vitro treatment of MMP-2 and MMP-9 significantly promoted both spreading and invasion of mouse trophoblastic cells compared to the non-treated blastocysts. Moreover, embryo transfer results showed that MMP-9 co-transfer enhanced pregnancy outcome inform of live pup rate by degrading the extracellular matrix, collagen, and facilitate embryo implantation. Taken together our findings imply that MMP-9 can regulate trophoblastic cell invasion during preimplantation, which may have important consequences on embryo implantation, and shed the light on new strategies to avoid miscarriage and provides a platform for successful human embryo transfer technologies.

摘要

成功的着床与 MMP-2 和 MMP-9 的表达密切相关,这极大地影响了胚胎降解子宫内膜上皮基底膜(主要由 IV 型胶原组成)并侵入子宫基质的能力。本研究旨在确定 MMP-2 和 MMP-9 与胚胎共转移对小鼠生殖性能的影响。通过侵袭实验,我们测试了 MMP-2 和 MMP-9 支持滋养层细胞体外侵袭的能力。我们使用非手术胚胎转移(NSET)技术将 MMP-2 和 MMP-9 与 2.5 天孕(dpc)假孕子宫中的小鼠胚胎共转移,并评估妊娠结局。收集子宫组织样本,通过 Masson 三色染色法测定胶原含量。我们的结果表明,与未经处理的囊胚相比,MMP-2 和 MMP-9 的体外处理显著促进了小鼠滋养层细胞的扩展和侵袭。此外,胚胎转移结果表明,MMP-9 的共转移通过降解细胞外基质、胶原促进胚胎着床,从而提高活产率,改善妊娠结局。综上所述,我们的研究结果表明 MMP-9 可以调节着床前滋养层细胞的侵袭,这可能对胚胎着床有重要影响,并为避免流产提供了新的策略,并为成功的人类胚胎转移技术提供了一个平台。

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