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人脐血管内皮细胞表达雌激素受体β(ERβ)和孕激素受体A(PR-A),但不表达雌激素受体α(ERα)和孕激素受体B(PR-B)。

Human umbilical vascular endothelial cells express estrogen receptor beta (ERbeta) and progesterone receptor A (PR-A), but not ERalpha and PR-B.

作者信息

Toth Bettina, Saadat Gitti, Geller Alrun, Scholz Christoph, Schulze Sandra, Friese Klaus, Jeschke Udo

机构信息

Department of Obstetrics and Gynecology, Grosshadern, Ludwig-Maximilians University, 81377, Munich, Germany.

出版信息

Histochem Cell Biol. 2008 Aug;130(2):399-405. doi: 10.1007/s00418-008-0426-7. Epub 2008 Apr 18.

Abstract

Several reports deal with possible effects of female sex hormones on human umbilical vein endothelial cells (HUVEC) including elasticity, activation of plasma membrane Na+/H+ exchange, VEGF receptor Flk-1/KDR and many others. In contrast to those findings, some publications pointed out that HUVEC lack expression of both the estrogen receptor (ER) and/or the progesterone receptor (PR). Because the majority of these investigations were carried out at a time period, when only one ER and one PR was known, the aim of this study was the systematic analysis of ERalpha and ERbeta as well as PR-A and PR-B expression in HUVEC with specific monoclonal antibodies by immunocytochemistry and quantitative RT-PCR (TaqMan). As a result, we could show that HUVEC lack ERalpha but express ERbeta. The expression of ERbeta could be significantly upregulated with 17beta-estradiol on mRNA and protein level. In addition, HUVEC express PR-A but not PR-B. PR-A expression could be significantly upregulated with progesterone, again on mRNA and protein level. We conclude that estrogenic effects on HUVEC are mediated via the ERbeta and gestagens act via the PR-A pathway.

摘要

有几份报告探讨了女性性激素对人脐静脉内皮细胞(HUVEC)的可能影响,包括弹性、质膜Na+/H+交换的激活、血管内皮生长因子(VEGF)受体Flk-1/KDR等诸多方面。与这些研究结果相反,一些出版物指出HUVEC缺乏雌激素受体(ER)和/或孕激素受体(PR)的表达。由于这些研究大多是在仅知晓一种ER和一种PR的时期进行的,本研究的目的是通过免疫细胞化学和定量逆转录聚合酶链反应(TaqMan),用特异性单克隆抗体对HUVEC中的ERα和ERβ以及PR-A和PR-B表达进行系统分析。结果,我们发现HUVEC缺乏ERα但表达ERβ。17β-雌二醇可使ERβ在mRNA和蛋白质水平上的表达显著上调。此外,HUVEC表达PR-A但不表达PR-B。孕激素同样可使PR-A在mRNA和蛋白质水平上的表达显著上调。我们得出结论,雌激素对HUVEC的作用是通过ERβ介导的,而孕激素则通过PR-A途径发挥作用。

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