Zhang Song-ying, Lin Xiao-na, Song Tao, Tong Xiao-mei, Shu Jing, Huang He-feng
Department of Gynecology and Obstetrics, Sir Run Run Shaw Hospital, Zhejiang University Medical College, Hangzhou 310016, China.
Zhonghua Yi Xue Za Zhi. 2008 Aug 26;88(33):2343-6.
To find valuable implantation-related genes associated with endometrial receptivity by scanning the complete genome array of endometrium at the luteal phase of superovulation cycle and the natural cycle.
Twenty endometrial samples were obtained from patients who were to undergo invitro fertilization and embryo transfer because of the ovarian or male factors, underwent real-time quantitative PCR (QPCR) to confirm the differentially expressed genes and pathological examination to confirm the stages. Five of the 20 endometrial samples from days of LH + 4, LH + 7, or HCG + 7 underwent HU133 plus2.0 microarray scanning. The other 15 samples were divided into 2 groups: 7 samples were taken on the day LH + 7, and 8 samples taken on the day HCG + 7.
581 genes were expressed differentially in the LH + 7 and LH + 4 samples: 395 were up-regulated and 186 were down-regulated. 320 genes were expressed differentially in the HCG + 7 and LH + 7 samples: 175 genes were up-regulated, and 145 genes were down-regulated. QPCR test showed that the expression levels of some up-regulated genes were much lower on the day HCG + 7 than on the day LH + 7, such as PAEP, S100P, SOD and GDF15.
Microarray scanning provides a global gene expression spectrum of human endometrium at different phases. A set of genes are active at the implantation window phase of endometrium. These genes don't show adequate expression after superovulation, which may lead to the change of endometrial receptivity.
通过扫描超排卵周期和自然周期黄体期子宫内膜的全基因组芯片,寻找与子宫内膜容受性相关的有价值的着床相关基因。
从因卵巢因素或男性因素而行体外受精-胚胎移植的患者中获取20份子宫内膜样本,进行实时定量PCR(QPCR)以确认差异表达基因,并进行病理检查以确认分期。对20份子宫内膜样本中来自LH+4天、LH+7天或HCG+7天的5份样本进行HU133 plus2.0芯片扫描。另外15份样本分为2组:7份样本在LH+7天采集,8份样本在HCG+7天采集。
在LH+7和LH+4样本中有581个基因差异表达:395个上调,186个下调。在HCG+7和LH+7样本中有320个基因差异表达:175个基因上调,145个基因下调。QPCR检测显示,一些上调基因在HCG+7天的表达水平比LH+7天低得多,如PAEP、S100P、SOD和GDF15。
芯片扫描提供了人类子宫内膜不同阶段的全基因组表达谱。一组基因在子宫内膜着床窗期活跃。这些基因在超排卵后未显示出足够的表达,这可能导致子宫内膜容受性的改变。