Global analyses and potential effects of extracellular vesicles on the establishment of conceptus implantation during the peri-implantation period.

IF 1.9 4区 生物学 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE Journal of Reproduction and Development Pub Date : 2023-10-20 Epub Date: 2023-07-25 DOI:10.1262/jrd.2023-044
Keigo Nakamura, Kazuya Kusama, Masatoshi Hori, Kazuhiko Imakawa
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Abstract

Intrauterine extracellular vesicles (EVs) are involved in establishing proper conceptus-endometrial communication, which is essential for conceptus implantation and subsequent successful placentation. Despite several studies on intrauterine EVs, the composition and quantitative changes in conceptus and endometrial EVs, as well as the effects of intrauterine EVs on endometrial epithelial cells (EECs) during the peri-implantation period, have not been well characterized. To elucidate global changes in proteins in EVs extracted from uterine flushings (UFs) during the pre-implantation (P17), just-implantation (P20), and post-implantation (P22) periods, the datasets of the proteome iTRAQ analysis were compared among P17, P20, and P22 EVs. These analyses revealed that the composition and function of proteins in the EVs changed dramatically during peri-implantation in cattle. Notably, intrauterine P17 EVs affected the high expression of "Developmental Biology" and "morphogenesis of an endothelium" compared with those in P20 and P22 EVs. Furthermore, P20 EVs had the functions of the high expression of "mitochondrial calcium ion homeostasis" and "Viral mRNA Translation" compared with those in P17 EVs. Transcripts extracted from EECs treated with P17, P20, or P22 EVs were subjected to RNA-seq analysis. These analyses identified 60 transcripts in EECs commonly induced by intrauterine EVs recovered from P17, P20, and P22, a large number of which were associated with "type I interferon signaling pathway". Collectively, these findings reveal the presence and multiple functions of EVs that are potentially implicated in facilitating conceptus implantation into the uterine epithelium during the peri-implantation period.

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细胞外小泡在胚胎植入期建立过程中的整体分析和潜在影响。
子宫内细胞外小泡(EVs)参与建立正确的妊娠-子宫内膜沟通,这对妊娠植入和随后成功的胎盘形成至关重要。尽管对宫内EVs进行了几项研究,但妊娠期和子宫内膜EVs的组成和数量变化,以及宫内EVs在植入期对子宫内膜上皮细胞(EECs)的影响,尚未得到很好的表征。为了阐明从子宫冲洗液(UFs)中提取的EV在植入前(P17)、刚植入(P20)和植入后(P22)期间蛋白质的总体变化,比较了P17、P20和P22 EV的蛋白质组iTRAQ分析数据集。这些分析表明,在牛胚胎植入期,EVs中蛋白质的组成和功能发生了巨大变化。值得注意的是,与P20和P22 EVs相比,宫内P17 EVs影响“发育生物学”和“内皮形态发生”的高表达。此外,与P17 EVs相比,P20 EVs具有“线粒体钙离子稳态”和“病毒mRNA翻译”的高表达功能。对从用P17、P20或P22-EVs处理的EECs提取的转录物进行RNA-seq分析。这些分析在EECs中鉴定了60个转录物,这些转录物通常由P17、P20和P22中回收的宫内EVs诱导,其中大量与“I型干扰素信号通路”有关。总之,这些发现揭示了EVs的存在和多种功能,这些功能可能与促进胚胎在胚胎植入期植入子宫上皮有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Reproduction and Development
Journal of Reproduction and Development 生物-奶制品与动物科学
CiteScore
3.70
自引率
11.10%
发文量
52
审稿时长
2 months
期刊介绍: Journal of Reproduction and Development (JRD) is the official journal of the Society for Reproduction and Development, published bimonthly, and welcomes original articles. JRD provides free full-text access of all the published articles on the web. The functions of the journal are managed by Editorial Board Members, such as the Editor-in-Chief, Co-Editor-inChief, Managing Editors and Editors. All manuscripts are peer-reviewed critically by two or more reviewers. Acceptance is based on scientific content and presentation of the materials. The Editors select reviewers and correspond with authors. Final decisions about acceptance or rejection of manuscripts are made by the Editor-in-Chief and Co-Editor-in-Chief.
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