Department of Obstetrics and Gynecology, Kansai Medical University, Osaka, Japan.
Fertil Steril. 2011 Sep;96(3):786-91. doi: 10.1016/j.fertnstert.2011.06.048. Epub 2011 Jul 20.
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.
In vitro experiment.
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.
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。
体外实验。
关西医科大学研究实验室。
因良性原因接受子宫切除术的 14 名患者。
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。
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。
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。
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。