Liu Xuemei, Zhu Guijin, Zhong Gang
Reproductive Medicine Center, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2007 Aug;27(4):464-7. doi: 10.1007/s11596-007-0430-5.
HOXA10 gene plays an essential role in differentiation of the endometrium and in human reproduction. The aim of this study was to investigate the regulatory effect of sex steroids and HB-EGF on HOXA10 gene in Ishikawa cells. Ishikawa cells were incubated with 17-beta estradiol (10(-8) mol/L), medroxyprogesterone acetate (MPA) (10(-6) mol/L), RU486 (10(-5) mol/L) or HB-EGF (10 ng/mL) for 48 h respectively. The expression of HOXA10 gene was detected by immunofluorescence, reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting. Our results showed that either estrogen alone, progestin alone or progestin combined with estrogen could significantly increase the expression of HOXA10 gene 48 h after the treatment (P<0.05). But estrogen combined with progestin and RU486 could inhibit the up-regulation by estrogen and progestin. HB-EGF could elevate the expression of HOXA10 gene 48 h after the treatment (P<0.05). It is concluded that both estrogen and progestin can up-regulate the expression of HOXA10 gene in Ishikawa cells, but RU486 can inhibit the effect and HB-EGF can elevate the expression level of HOXA10 gene.
HOXA10基因在子宫内膜分化和人类生殖过程中发挥着至关重要的作用。本研究旨在探讨性激素和肝素结合表皮生长因子(HB-EGF)对Ishikawa细胞中HOXA10基因的调控作用。分别用17-β雌二醇(10⁻⁸mol/L)、醋酸甲羟孕酮(MPA)(10⁻⁶mol/L)、米非司酮(RU486)(10⁻⁵mol/L)或HB-EGF(10 ng/mL)处理Ishikawa细胞48小时。通过免疫荧光、逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法检测HOXA10基因的表达。我们的结果显示,单独使用雌激素、单独使用孕激素或孕激素与雌激素联合使用均可在处理48小时后显著增加HOXA10基因的表达(P<0.05)。但雌激素与孕激素及RU486联合使用可抑制雌激素和孕激素引起的上调作用。HB-EGF可在处理48小时后提高HOXA10基因的表达(P<0.05)。结论是,雌激素和孕激素均可上调Ishikawa细胞中HOXA1基因的表达,但RU486可抑制该作用,而HB-EGF可提高HOXA10基因的表达水平。