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氯离子细胞内通道 4 在不孕女性的子宫内膜中失调,并改变了接受能力。

Chloride intracellular channel 4 is dysregulated in endometrium of women with infertility and alters receptivity.

机构信息

Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Victoria, 3010, Australia; Gynaecology Research Centre, Royal Women's Hospital, Parkville, Victoria, 3052, Australia.

Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Victoria, 3010, Australia; Gynaecology Research Centre, Royal Women's Hospital, Parkville, Victoria, 3052, Australia.

出版信息

Biochem Biophys Res Commun. 2020 Oct 22;531(4):490-496. doi: 10.1016/j.bbrc.2020.07.046. Epub 2020 Aug 15.

Abstract

The endometrium remodels in each menstrual cycle to become receptive in preparation for embryo implantation which occurs in the mid-secretory phase of the cycle. Failure of blastocyst adhesion and implantation cause infertility. We compared chloride intracellular channel 4 (CLIC4) expression in human endometrium from women with normal fertility and primary unexplained infertility in the mid-secretory/receptive phase of the menstrual cycle. CLIC4 localised to both the epithelial and stromal regions of the endometrium of fertile tissues across the cycle. CLIC4 expression was significantly reduced in the luminal and glandular epithelium and remained unchanged in the stromal region of mid-secretory infertile endometrium compared to fertile endometrium. siRNA knockdown of CLIC4 significantly compromised adhesive capacity of Ishikawa cells (endometrial epithelial cell line). This reduced adhesion and CLIC4 expression was associated with elevated SGK1, p53, SIRT1, BCL2 and MCL1 gene expression in the Ishikawa cells. CLIC4 expression was increased in primary human endometrial stromal cells during decidualization, however, siRNA knockdown of CLIC4 did not affect decidualization. Our data provide evidence that CLIC4 may regulate receptivity and facilitate blastocyst attachment initiating implantation. Reduced CLIC4 levels may be causative of implantation failure in women.

摘要

子宫内膜在每个月经周期中进行重塑,以变得对胚胎植入具有接受性,而胚胎植入发生在周期的中分泌期。胚泡黏附和植入的失败导致不孕。我们比较了在月经周期的中分泌/接受期,正常生育和原发性不明原因不孕的妇女的人子宫内膜中氯离子通道 4(CLIC4)的表达。CLIC4 定位于肥沃组织的子宫内膜的上皮和基质区域。与肥沃的子宫内膜相比,中分泌期不孕子宫内膜的腔上皮和腺上皮中的 CLIC4 表达显著降低,而基质区域中的 CLIC4 表达保持不变。CLIC4 的 siRNA 敲低显着损害了 Ishikawa 细胞(子宫内膜上皮细胞系)的黏附能力。这种降低的黏附和 CLIC4 表达与 Ishikawa 细胞中 SGK1、p53、SIRT1、BCL2 和 MCL1 基因表达的升高相关。在蜕膜化过程中,人子宫内膜基质细胞中的 CLIC4 表达增加,然而,CLIC4 的 siRNA 敲低并不影响蜕膜化。我们的数据提供了证据,表明 CLIC4 可能调节接受性并促进启动植入的胚泡附着。CLIC4 水平降低可能是导致妇女植入失败的原因。

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