Cellular prion: a novel regulator of decidual cell function at the maternal-fetal interface.

IF 3.6 2区 医学 Q2 DEVELOPMENTAL BIOLOGY
Swarnali Dey, Tamal Kanti Gope, Rupasri Ain
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引用次数: 0

Abstract

Cellular prion (PRNP) is a GPI-anchored extrinsic membrane glycoprotein, which has been implicated in mouse decidualization. However, the molecular function of this protein in mouse decidua is not known. In this article, we have characterized and elucidated the possible role of PRNP in mouse decidua. We demonstrated that PRNP expression is evident on embryonic day (E) 6.5 to E9.5 across the primary decidual zone (PDZ) in the mouse implantation site. As gestation progressed, PRNP continued to be expressed in the receding decidua, up to E17.5. shRNA-mediated knockdown of PRNP on E5.5 through E7.5 led to decreased expression of tight junction proteins (TJPs) in PDZ in vivo. These included Cingulin, Afadin, Catenin-α1, Lethal (2) giant larvae protein homolog 1, Claudin-5, and ICAM1. Furthermore, PRNP-positive decidual cells showed augmented expression of autophagic machinery. PRNP knockdown curtailed expression of autophagy-related genes in decidua in vivo. Our results highlight hitherto unknown novel functions of PRNP: (i) an inducer of TJPs at PDZ, which protects the developing embryo and (ii) a decision-maker protein between life and death in decidual cells.

细胞朊病毒:一种新的母胎界面的蜕细胞功能调节剂。
细胞朊病毒(PRNP)是一种GPI锚定的外源性膜糖蛋白,与小鼠脱个体化有关。然而,该蛋白在小鼠蜕膜中的分子功能尚不清楚。在本报告中,我们描述并阐明了PRNP在小鼠蜕膜中的可能作用。我们发现,PRNP在胚胎日(E) 6.5至E9.5期间在小鼠着床部位的初级蜕膜区(PDZ)有明显表达。随着妊娠的进展,PRNP继续在退蜕膜中表达,达到E17.5。shrna介导的E5.5到E7.5上PRNP的敲低导致PDZ体内紧密连接蛋白(TJPs)的表达降低。其中包括CINGULIN、AFADIN、CATENIN-α1、致死(2)巨幼虫蛋白同源物1、Caludin-5和ICAM-1。此外,prnp阳性的蜕细胞表现出自噬机制的增强表达。PRNP敲除抑制蜕膜中自噬相关基因的表达。我们的研究结果突出了迄今为止未知的PRNP的新功能:a)在PDZ上诱导TJPs,保护发育中的胚胎;b)在蜕细胞中是生死之间的决策者蛋白。
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
Molecular human reproduction
Molecular human reproduction 生物-发育生物学
CiteScore
8.30
自引率
0.00%
发文量
37
审稿时长
6-12 weeks
期刊介绍: MHR publishes original research reports, commentaries and reviews on topics in the basic science of reproduction, including: reproductive tract physiology and pathology; gonad function and gametogenesis; fertilization; embryo development; implantation; and pregnancy and parturition. Irrespective of the study subject, research papers should have a mechanistic aspect.
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