郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2014年
2期
215-218
,共4页
刘子霞%赵华%王兴玲%徐玲
劉子霞%趙華%王興玲%徐玲
류자하%조화%왕흥령%서령
不孕症%子宫内膜容受性%HOXA-11基因%雌激素受体%孕激素受体
不孕癥%子宮內膜容受性%HOXA-11基因%雌激素受體%孕激素受體
불잉증%자궁내막용수성%HOXA-11기인%자격소수체%잉격소수체
sterility%endometrial receptivity%HOXA-11 gene%estrogen receptor%progesterone receptor
目的:探讨雌孕激素受体(ER、PR)及同源框基因-11(HOXA-11)在人子宫内膜种植窗口期的表达。方法:采用免疫组化和RT-PCR方法检测ER、PR及HOXA-11在拟行IVF-ET患者排卵后子宫内膜种植窗口期的表达。按IVF-ET后是否妊娠将153例因输卵管因素不孕的患者分为未妊娠组(n=86)和妊娠组(n=67)。结果:免疫组化结果显示PR和HOXA-11在妊娠组腺上皮细胞中的表达均低于未妊娠组( P均<0.001),在间质细胞中的表达均高于未妊娠组(P均<0.001)。 RT-PCR 结果显示妊娠组子宫内膜 ER、PR 及 HOXA-11 mRNA 的相对表达量均高于未妊娠组(P均<0.05)。 P水平与腺上皮、间质PR及腺上皮HOXA-11蛋白表达有关(P均<0.05)。结论:种植窗口期内膜腺上皮PR、HOXA-11表达下调和间质细胞PR、HOXA-11表达上调的失败可能是导致子宫内膜容受性下降的原因之一。
目的:探討雌孕激素受體(ER、PR)及同源框基因-11(HOXA-11)在人子宮內膜種植窗口期的錶達。方法:採用免疫組化和RT-PCR方法檢測ER、PR及HOXA-11在擬行IVF-ET患者排卵後子宮內膜種植窗口期的錶達。按IVF-ET後是否妊娠將153例因輸卵管因素不孕的患者分為未妊娠組(n=86)和妊娠組(n=67)。結果:免疫組化結果顯示PR和HOXA-11在妊娠組腺上皮細胞中的錶達均低于未妊娠組( P均<0.001),在間質細胞中的錶達均高于未妊娠組(P均<0.001)。 RT-PCR 結果顯示妊娠組子宮內膜 ER、PR 及 HOXA-11 mRNA 的相對錶達量均高于未妊娠組(P均<0.05)。 P水平與腺上皮、間質PR及腺上皮HOXA-11蛋白錶達有關(P均<0.05)。結論:種植窗口期內膜腺上皮PR、HOXA-11錶達下調和間質細胞PR、HOXA-11錶達上調的失敗可能是導緻子宮內膜容受性下降的原因之一。
목적:탐토자잉격소수체(ER、PR)급동원광기인-11(HOXA-11)재인자궁내막충식창구기적표체。방법:채용면역조화화RT-PCR방법검측ER、PR급HOXA-11재의행IVF-ET환자배란후자궁내막충식창구기적표체。안IVF-ET후시부임신장153례인수란관인소불잉적환자분위미임신조(n=86)화임신조(n=67)。결과:면역조화결과현시PR화HOXA-11재임신조선상피세포중적표체균저우미임신조( P균<0.001),재간질세포중적표체균고우미임신조(P균<0.001)。 RT-PCR 결과현시임신조자궁내막 ER、PR 급 HOXA-11 mRNA 적상대표체량균고우미임신조(P균<0.05)。 P수평여선상피、간질PR급선상피HOXA-11단백표체유관(P균<0.05)。결론:충식창구기내막선상피PR、HOXA-11표체하조화간질세포PR、HOXA-11표체상조적실패가능시도치자궁내막용수성하강적원인지일。
Aim:To investigate the expressions of ER , PR and HOXA-11 in human endometrium during window peri-od.Methods:Using immunohistochemical staining and RT-PCR the expressions of ER , PR and HOXA-11 in human endo-metrium during the window period were detected .According to pregnancy or not after IVF-ET, 78 cases of infertility pa-tients with tubal factors were divided into pregnant group ( n=86 ) and non-pregnant group ( n=67 ) .Results: The ex-pressions of PR and HOXA-11 in the glandular epithelium of the pregnant group were significantly lower than those of the non-pregnant group(P<0.001), while in the stromal cells were significantly higher than those of the non-pregnant group (P<0.001).The expressions of ER,PR and HOXA-11 mRNA of the pregnant group were higher than those of the non-pregnant group(P<0.05).There was correlation between level of P and PR,HOXA-11 in glandular epithelial(P<0.05). Conclusion:The down-regulated expressions of PR and HOXA-11 in glandular epithelial cells and the up-regulated expres-sions of PR and HOXA-11 in mesenchymal cells may be the reasons which lead to the decrease of endometrial receptivity .