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雌二醇可诱导人子宫内膜中乙酰肝素酶-1的表达及硫酸乙酰肝素蛋白聚糖的降解。

Estradiol induces heparanase-1 expression and heparan sulphate proteoglycan degradation in human endometrium.

作者信息

Xu Xiulong, Ding Jianchi, Rao Geetha, Shen Jikun, Prinz Richard A, Rana Nasir, Dmowski W Paul

机构信息

Department of General Surgery, Rush University Medical Center, Chicago, IL 60612, USA.

出版信息

Hum Reprod. 2007 Apr;22(4):927-37. doi: 10.1093/humrep/del483. Epub 2007 Jan 29.

Abstract

BACKGROUND

This study seeks to determine whether estrogen is able to regulate the expression of heparanase-1 (HPR1) in human endometrium.

METHODS

HPR1 expression and heparan sulphate (HS) deposition in the endometrium collected in various menstrual phases were analysed by immunohistochemical and immunofluorescence staining, respectively. HPR1 expression in the endometrial cells unexposed or exposed to estradiol was analysed by using RT-PCR and luciferase reporter assay. HPR1 activity was analysed by using a novel enzyme-linked immunosorbent assay (ELISA). Cell surface HS levels were analysed by flow cytometry. Serum HPR1 activity in women receiving follicle-stimulating hormone (FSH) for IVF was measured by ELISA.

RESULTS

HPR1 expression was rarely detected in the endometrium in the early and mid-proliferative phases but was increased in the late proliferative phase and in the secretory phases. HPR1 expression was negatively associated with HS in the basement membrane (BM) of the endometrial glands. HPR1 gene expression, HPR1 promoter activity and HPR1 enzymatic activity were increased in the endometrial cells when exposed to 17beta-estradiol (E(2)), whereas cell surface HS levels showed a decrease which could be blocked by PI-88, an HPR1 inhibitor. Serum HPR1 levels were increased in women with moderately elevated blood estrogen levels after receiving FSH.

CONCLUSIONS

HPR1 is differentially expressed in the endometrium in different menstrual phases. Estrogen plays an important role in inducing HPR1 expression, subsequently leading to HS degradation on the endometrial cell surface and in the BM of the endometrium.

摘要

背景

本研究旨在确定雌激素是否能够调节人子宫内膜中乙酰肝素酶-1(HPR1)的表达。

方法

分别通过免疫组织化学和免疫荧光染色分析在不同月经周期收集的子宫内膜中HPR1的表达和硫酸乙酰肝素(HS)的沉积。使用逆转录聚合酶链反应(RT-PCR)和荧光素酶报告基因检测分析未暴露或暴露于雌二醇的子宫内膜细胞中HPR1的表达。使用新型酶联免疫吸附测定(ELISA)分析HPR1活性。通过流式细胞术分析细胞表面HS水平。通过ELISA测量接受体外受精促卵泡激素(FSH)的女性血清HPR1活性。

结果

在增殖早期和中期的子宫内膜中很少检测到HPR1表达,但在增殖后期和分泌期增加。子宫内膜腺基底膜(BM)中的HPR1表达与HS呈负相关。当暴露于17β-雌二醇(E₂)时,子宫内膜细胞中的HPR1基因表达、HPR1启动子活性和HPR1酶活性增加,而细胞表面HS水平降低,这可被HPR1抑制剂PI-88阻断。接受FSH后血雌激素水平中度升高的女性血清HPR1水平升高。

结论

HPR1在不同月经周期的子宫内膜中差异表达。雌激素在诱导HPR1表达中起重要作用,随后导致子宫内膜细胞表面和子宫内膜BM中的HS降解。

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