内质网应激反应和子宫内膜干扰素- β产生的调节

Ramya Sethuram M.D. , Melissa Bukowski B.Sc. , Francis Hernandez B.Sc. , Yuan You B.Sc. , Elizabeth Puscheck M.D. , Gil Mor M.D. , Pancharatnam Jeyasuria Ph.D. , Jennifer C. Condon Ph.D.
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引用次数: 0

摘要

目的了解内质网应激在妊娠早期子宫内膜室中的潜在作用,这是一个研究不足的区域。设计本研究在体外检测了人蜕膜化和非蜕膜化子宫内膜细胞(人子宫内膜基质细胞[HESCs])中干扰素-β(IFNβ)对ER应激反应的调节。在体内,我们在胚胎期(E)1、E3和E6植入前后,局部检测了小鼠子宫内膜的ER应激和IFNβ水平。设置该研究在人类生长发育的生殖科学实验室进行。患者无。干预无。主要结果测量定量聚合酶链反应、蛋白质印迹,免疫组织化学分析使我们能够测试子宫内膜室中可能由植入物触发的内源性ER应激激活的作用及其增加子宫内膜IFNβ水平的能力。结果(s)在体外,我们观察到HESC中的IFNβ水平存在显著差异,这是对ER应激激活的反应,其中蜕膜化的HESC表现出与非蜕膜化HESC相比IFNβ含量增加了三倍。由于ER应激依赖性抑制核因子κβ调节的抗凋亡因子XIAP和MCL-1,凋亡胱天蛋白酶-3的激活也被分离到蜕膜化细胞中。在体内,小鼠子宫内膜IFNβ在所检查的所有时间点都存在于F4/80阳性巨噬细胞中。植入(E6)后,小鼠管腔上皮细胞强烈共表达IFNβ和ER应激标志物免疫球蛋白重链结合蛋白(BiP)。结论(s)这些分析表明,在体内外,经历ER应激的分化和蜕膜化子宫内膜细胞都有能力产生增加的IFNβ水平;因此,子宫内膜室的ER应激激活可能在促进成功植入事件中起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endoplasmic reticulum stress response and the regulation of endometrial interferon-beta production

Objective

To gain an understanding of the potential role of endoplasmic reticulum (ER) stress in the endometrial compartment during early pregnancy, a highly understudied area.

Design

This study examined the regulation of interferon-β (IFNβ) in response to ER stress in human decidualized and nondecidualized endometrial cells (human endometrial stromal cells [HESCs]) in vitro. In vivo, we examined ER stress and the IFNβ levels locally in the mouse endometrium before and after implantation at embryonic day (E)1, E3, and E6.

Setting

The study was performed in a reproductive sciences laboratory for Human Growth and Development.

Patient(s)

None.

Intervention(s)

None.

Main Outcome Measure(s)

Quantitative polymerase chain reaction, Western blotting, and immunohistochemical analysis allowed us to test the action of endogenous ER stress activation in the endometrial compartment likely triggered by implantation and its ability to increase the endometrial IFNβ levels.

Result(s)

In vitro, we observed a significant difference in the IFNβ levels in HESCs, in response to ER stress activation, where decidualized HESCs exhibited a threefold increase in the IFNβ levels compared with nondecidualized HESCs. Apoptotic caspase-3 activation was also isolated to the decidualized cells as a result of ER stress–dependent suppression of nuclear factor-kappa beta–regulated antiapoptotic factors, XIAP and MCL-1. In vivo, mouse endometrial IFNβ was present in F4/80-positive macrophages at all time points examined. After implantation (E6), the mouse luminal epithelial cells robustly coexpressed both IFNβ and the ER stress marker immunoglobulin heavy chain binding protein (BiP).

Conclusion(s)

These analyses demonstrate that both in vivo and in vitro, differentiated and decidualized endometrial cells undergoing ER stress have the capacity to produce increased IFNβ levels; therefore, ER stress activation in the endometrial compartment may play a vital role in promoting successful implantation events.

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来源期刊
F&S science
F&S science Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Urology
CiteScore
2.00
自引率
0.00%
发文量
0
审稿时长
51 days
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