上海交通大学学报(医学版)
上海交通大學學報(醫學版)
상해교통대학학보(의학판)
JOURNAL OF SHANGHAI JIAOTONG UNIVERSITY(MEDICAL SCIENCE)
2009年
7期
833-836,881
,共5页
陈秋菊%程利南%李路%高晓红%吴煜%孙兆贵%王健%孙晓溪
陳鞦菊%程利南%李路%高曉紅%吳煜%孫兆貴%王健%孫曉溪
진추국%정리남%리로%고효홍%오욱%손조귀%왕건%손효계
基因芯片%筛查%子宫内膜%控制性超排卵
基因芯片%篩查%子宮內膜%控製性超排卵
기인심편%사사%자궁내막%공제성초배란
microarray%screening%endometrium%controlled ovarian hyperstimulation
目的 研究控制性超排卵过程中卵巢高反应者围着床期子宫内膜基因表达谱的变化.方法 超排卵过程中因出现卵巢高反应而取消胚胎移植的妇女(高反应组,n=4)和有正常生育史的育龄妇女(对照组,n=3),分别于围着床期行子宫内膜组织活检术.HE染色观察子宫内膜组织学改变;基因芯片Affymetrix U133A 2.0筛选差异表达基因,Real-time PCR加以验证;应用生物信息学分析工具PANTHER进行差异表达基因的生物学过程分析.结果 对照组子宫内膜均为分泌中期,高反应组子宫内膜部分腺体发育延迟.筛选出差异表达基因364个,其中上调基因233个,下调基因131个;Real-time PCR验证与子宫内膜功能相关基因OPN、PLA2G2、DPPIV、IGFBP5和SSAT,每个基因的Real-time PCR结果与芯片检测的信号值呈显著正相关(r=0.44,P<0.01).PANTHER分析显示,差异表达基因参与细胞因子信号转导和免疫调节等生物学过程.结论 卵巢高反应影响围着床期子宫内膜的基因表达,可能是高甾体激素使子宫内膜接受性降低的机制之一.
目的 研究控製性超排卵過程中卵巢高反應者圍著床期子宮內膜基因錶達譜的變化.方法 超排卵過程中因齣現卵巢高反應而取消胚胎移植的婦女(高反應組,n=4)和有正常生育史的育齡婦女(對照組,n=3),分彆于圍著床期行子宮內膜組織活檢術.HE染色觀察子宮內膜組織學改變;基因芯片Affymetrix U133A 2.0篩選差異錶達基因,Real-time PCR加以驗證;應用生物信息學分析工具PANTHER進行差異錶達基因的生物學過程分析.結果 對照組子宮內膜均為分泌中期,高反應組子宮內膜部分腺體髮育延遲.篩選齣差異錶達基因364箇,其中上調基因233箇,下調基因131箇;Real-time PCR驗證與子宮內膜功能相關基因OPN、PLA2G2、DPPIV、IGFBP5和SSAT,每箇基因的Real-time PCR結果與芯片檢測的信號值呈顯著正相關(r=0.44,P<0.01).PANTHER分析顯示,差異錶達基因參與細胞因子信號轉導和免疫調節等生物學過程.結論 卵巢高反應影響圍著床期子宮內膜的基因錶達,可能是高甾體激素使子宮內膜接受性降低的機製之一.
목적 연구공제성초배란과정중란소고반응자위착상기자궁내막기인표체보적변화.방법 초배란과정중인출현란소고반응이취소배태이식적부녀(고반응조,n=4)화유정상생육사적육령부녀(대조조,n=3),분별우위착상기행자궁내막조직활검술.HE염색관찰자궁내막조직학개변;기인심편Affymetrix U133A 2.0사선차이표체기인,Real-time PCR가이험증;응용생물신식학분석공구PANTHER진행차이표체기인적생물학과정분석.결과 대조조자궁내막균위분비중기,고반응조자궁내막부분선체발육연지.사선출차이표체기인364개,기중상조기인233개,하조기인131개;Real-time PCR험증여자궁내막공능상관기인OPN、PLA2G2、DPPIV、IGFBP5화SSAT,매개기인적Real-time PCR결과여심편검측적신호치정현저정상관(r=0.44,P<0.01).PANTHER분석현시,차이표체기인삼여세포인자신호전도화면역조절등생물학과정.결론 란소고반응영향위착상기자궁내막적기인표체,가능시고치체격소사자궁내막접수성강저적궤제지일.
Objective To investigate the gene expression profiles of peri-implantation endometrium of high responders during controlled ovarian hyperstimulation. Methods High responders with cancelled embryo-transfer during controlled ovarian hyperstimulation (high responder group, n=4) and healthy fertile volunteers (control group, n=3) were performed endometrial biopsies during peri-implantation. Histologic changes of endometrium were observed by HE staining, genes of differential expression were screened with microarrays Affymetrix U133A 2.0 and identified by Real-time PCR. The biological process analysis was performed by online biological information analysis tool PANTHER. Results The ehdometrium was in mid-secretory phase in control group, while development delay was found in some glandular organs in endometrium of high responder group. Three hundred and sixty-four genes of differential expression were screened, among which 233 were up-regulated genes and 131 were down-regulated genes. OPN, PLA2G2, DPPIV, IGFBP5 and SSAT were identified as endometrial function-related genes, whose Real-time PCR findings were positively correlated to gene signal values detected by microarray(r=0.44, P<0.01). PANTHER analysis indicated that genes of differential expression participated in the biological processes of cytokine signal transduction and immunological regulation. Conclusion Ovarian high response affects the gene expression profiles of peri-implantation endometrium, which may be one of the causes of sub-optimal endometrial receptivity.