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孕激素抑制雌二醇诱导的人子宫内膜基质细胞中血管内皮生长因子和基质细胞衍生因子 1。

Progestins inhibit estradiol-induced vascular endothelial growth factor and stromal cell-derived factor 1 in human endometrial stromal cells.

机构信息

Department of Obstetrics and Gynecology, Kansai Medical University, Osaka, Japan.

出版信息

Fertil Steril. 2011 Sep;96(3):786-91. doi: 10.1016/j.fertnstert.2011.06.048. Epub 2011 Jul 20.

Abstract

OBJECTIVE

To investigate whether 17β-estradiol (E(2)) and progestins exert direct effects on vascular endothelial growth factor (VEGF) and stromal cell-derived factor 1 (SDF-1/CXCL12) in human endometrial stromal cells (ESCs) and thereby to clarify the regulatory function of these local angiogenic factors in the endometrium.

DESIGN

In vitro experiment.

SETTING

Research laboratory at Kansai Medical University.

PATIENT(S): Fourteen patients undergoing hysterectomy for benign reasons.

INTERVENTION(S): ESCs were cultured with E(2) and/or various clinically relevant progestins (medroxyprogesterone acetate [MPA], norethisterone [NET], levonorgestrel [LNG], dienogest [DNG], and progesterone [P]).

MAIN OUTCOME MEASURE(S): The mRNA levels and production of VEGF and SDF-1 were assessed by real-time reverse-transcription polymerase chain reaction and ELISA, respectively.

RESULT(S): E(2) significantly induced the mRNA levels and protein production of VEGF and SDF-1 in ESCs. MPA could antagonize the E(2)-stimulated effects in a time- and dose-dependent manner, and this effect could be reversed by RU-486 (P receptor antagonist). All of the progestins (MPA, NET, LNG, and DNG; 10(-9) to 10(-7) mol/L) attenuated E(2)-induced VEGF and SDF-1 production, whereas P showed these inhibitory effects only when present in a high concentration (10(-7) mol/L).

CONCLUSION(S): Progestins have inhibitory effects on E(2)-induced VEGF and SDF-1 in ESCs. These results may indicate a potential mechanism for action of the female sex steroids in the human endometrium that can be helpful for various clinical applications.

摘要

目的

研究 17β-雌二醇(E2)和孕激素是否对人子宫内膜基质细胞(ESCs)中的血管内皮生长因子(VEGF)和基质细胞衍生因子 1(SDF-1/CXCL12)产生直接作用,从而阐明这些局部血管生成因子在子宫内膜中的调节功能。

设计

体外实验。

地点

关西医科大学研究实验室。

患者

因良性原因接受子宫切除术的 14 名患者。

干预措施

用 E2 和/或各种临床相关孕激素(醋酸甲羟孕酮[MPA]、炔诺酮[NET]、左炔诺孕酮[LNG]、地诺孕素[DNG]和孕酮[P])培养 ESCs。

主要观察指标

通过实时逆转录聚合酶链反应和 ELISA 分别评估 VEGF 和 SDF-1 的 mRNA 水平和产生。

结果

E2 显著诱导 ESCs 中 VEGF 和 SDF-1 的 mRNA 水平和蛋白产生。MPA 可以时间和剂量依赖性拮抗 E2 刺激的作用,而这种作用可以被 RU-486(P 受体拮抗剂)逆转。所有孕激素(MPA、NET、LNG 和 DNG;10(-9)至 10(-7)mol/L)均减弱了 E2 诱导的 VEGF 和 SDF-1 产生,而 P 仅在高浓度(10(-7)mol/L)时才表现出这些抑制作用。

结论

孕激素对 ESCs 中 E2 诱导的 VEGF 和 SDF-1 具有抑制作用。这些结果可能表明女性性激素在人类子宫内膜中的作用机制,这对各种临床应用可能有帮助。

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