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米非司酮对小鼠着床期子宫内膜活化的β-连环蛋白(active β-catenin)表达的影响
引用本文:陈世知,何俊琳,刘学庆,丁裕斌,黄静,陈雪梅,王应雄.米非司酮对小鼠着床期子宫内膜活化的β-连环蛋白(active β-catenin)表达的影响[J].生殖与避孕,2009,29(8):489-493.
作者姓名:陈世知  何俊琳  刘学庆  丁裕斌  黄静  陈雪梅  王应雄
作者单位:1. 重庆医科大学生殖生物学研究室、遗传优生教研室,重庆,400016;重庆医科大学附属第二医院,重庆,400010
2. 重庆医科大学生殖生物学研究室、遗传优生教研室,重庆,400016
基金项目:重庆市自然科学基金重点项目
摘    要:目的:探讨活化的β-连环蛋白(active β-catenin)在胚胎着床过程中的作用。方法:将孕第2日(d2)昆明小鼠随机分成3组,每组30只,A组:孕d2单次背部皮下注射0.1ml米非司酮(1.2mg/ml);B组(溶剂对照):以等量1,3-丙二醇代替米非司酮;C组:不作任何处理。用免疫组织化学、间接免疫荧光、Western blotting方法定性、定量、定位检测3组小鼠在妊娠d3 ̄7活化的β-连环蛋白的动态表达。结果:B、C组小鼠子宫内膜中活化的β-连环蛋白于孕d3在腺上皮和腔上皮、基质细胞质和细胞膜表达;妊娠d4在腔上皮细胞质和细胞膜强表达,并达高峰;妊娠d5 ̄7在腺上皮、血管内皮、腔上皮下基质细胞膜和细胞质表达,且B、C组间在妊娠d3 ̄7各时间点的表达无显著性差异(P>0.05);A组小鼠妊娠d3 ̄7活化的β-连环蛋白的表达较B、C组显著降低(P<0.01),在妊娠d4表达量未见高峰,且表达部位局限于基质细胞,腔上皮无表达。结论:米非司酮可能通过抑制孕激素与其受体结合而下调活化的β-连环蛋白表达,进而抑制子宫内膜黏附性,影响子宫内膜容受性的建立而阻碍胚胎顺利着床。

关 键 词:米非司酮  活化的β-连环蛋白(active  β-catenin)  子宫内膜  胚胎着床  小鼠

Effect of Mifepristone on the Expression of Active β-Catenin in Endometrium during the Peri-implantation Period in Mouse
Shi-zhi CHEN,Jun-lin HE,Xue-qing LIU,Yu-bin DING,Jing HUANG,Xue-mei CHEN,Ying-xiong WANG.Effect of Mifepristone on the Expression of Active β-Catenin in Endometrium during the Peri-implantation Period in Mouse[J].Reproduction and Contraception,2009,29(8):489-493.
Authors:Shi-zhi CHEN  Jun-lin HE  Xue-qing LIU  Yu-bin DING  Jing HUANG  Xue-mei CHEN  Ying-xiong WANG
Institution:Shi-zhi CHEN,Jun-lin HE,Xue-qing LIU,Yu-bin DING,Jing HUANG,Xue-mei CHEN,Ying-xiong WANG(1.Laboratory of reproductive biology,Department of Genetics,Chongqing Medical University,Chongqing,400016)(2.The Second Affiliated Hospital,Chongqing Medical University,Chongqing,400010)
Abstract:Objective:To explore the effect of mifepristone in the embryo implantation of pregnant mice.Methods:Kunming mice on pregnant day 2 were randomly divided into 3 groups with 30 in each group:mifepristone group(group A)was administered with 0.1 ml mifepristone(1.2 mg/ml)by hyodermic on backside;propylene glycol control group(group B)was administered 1,3 propylene glyccol instead of mifepristone with same dose;blank control group(group C)with no treatment.Expression of active β-catenin protein in endometrium of pregnant mice was detect from day 3 to day 7 of pregnancy by immunohistochemistry,Western blotting and immunofluorescence.Results:The expression of active β-catenin protein was significantly increased and reached its peak on pregnant day 4 in group B and group C,but there was no difference in the expression of active β-catenin between the two groups(P0.05).The levels of active β-catenin protein in group A were significantly lower than those in groups B and C(P0.01),and there was no peak expression on pregnant day 4.Conclusion:Mifepristone probably down-regulated the expression of β-catenin through inhibiting progestogen combined with its receptor,furthermore inhibited the adhesion of endometrium and influenced the establishment of endometrial receptivity,so as to obstruct the embryo implantation.
Keywords:mifepristone  endometrium  implantation  active β-catenin  mouse
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