新医学
新醫學
신의학
New Medicine
2015年
9期
580-583
,共4页
侯文汇%李银广%李珠玉%李婕%方利元%李小青%游泽山
侯文彙%李銀廣%李珠玉%李婕%方利元%李小青%遊澤山
후문회%리은엄%리주옥%리첩%방리원%리소청%유택산
不明原因复发性自然流产%叉头样转录因子 P3%基因启动子%甲基化
不明原因複髮性自然流產%扠頭樣轉錄因子 P3%基因啟動子%甲基化
불명원인복발성자연유산%차두양전록인자 P3%기인계동자%갑기화
Unexplained recurrent spontaneous abortion%FOXP3%Promoter%Methylation
目的:探讨不明原因复发性自然流产(URSA)患者蜕膜组织中叉头样转录因子 P3(FOXP3)基因的蛋白表达水平及其与启动子甲基化水平的关系。方法利用蛋白印迹法检测20例URSA 患者(URSA 组)和20名正常妊娠主动要求人工流产术的健康妇女(正常对照组)蜕膜组织中FOXP3蛋白表达情况,利用结合重亚硫酸盐的测序法(BSP)检测2组 FOXP3基因启动子甲基化情况,并分析两者的相关性。结果URSA 组蜕膜组织中 FOXP3表达水平明显低于正常对照组(P <0.01)。BSP 显示 URSA 组 FOXP3基因启动子甲基化水平明显高于正常对照组(P <0.01)。FOXP3蛋白表达水平与 FOXP3基因启动子甲基化水平呈负相关(r =-0.917,P <0.01)。结论FOXP3基因启动子甲基化水平升高后,FOXP3基因蛋白表达水平下调,引起免疫耐受异常,可能导致 RSA 的发病。
目的:探討不明原因複髮性自然流產(URSA)患者蛻膜組織中扠頭樣轉錄因子 P3(FOXP3)基因的蛋白錶達水平及其與啟動子甲基化水平的關繫。方法利用蛋白印跡法檢測20例URSA 患者(URSA 組)和20名正常妊娠主動要求人工流產術的健康婦女(正常對照組)蛻膜組織中FOXP3蛋白錶達情況,利用結閤重亞硫痠鹽的測序法(BSP)檢測2組 FOXP3基因啟動子甲基化情況,併分析兩者的相關性。結果URSA 組蛻膜組織中 FOXP3錶達水平明顯低于正常對照組(P <0.01)。BSP 顯示 URSA 組 FOXP3基因啟動子甲基化水平明顯高于正常對照組(P <0.01)。FOXP3蛋白錶達水平與 FOXP3基因啟動子甲基化水平呈負相關(r =-0.917,P <0.01)。結論FOXP3基因啟動子甲基化水平升高後,FOXP3基因蛋白錶達水平下調,引起免疫耐受異常,可能導緻 RSA 的髮病。
목적:탐토불명원인복발성자연유산(URSA)환자세막조직중차두양전록인자 P3(FOXP3)기인적단백표체수평급기여계동자갑기화수평적관계。방법이용단백인적법검측20례URSA 환자(URSA 조)화20명정상임신주동요구인공유산술적건강부녀(정상대조조)세막조직중FOXP3단백표체정황,이용결합중아류산염적측서법(BSP)검측2조 FOXP3기인계동자갑기화정황,병분석량자적상관성。결과URSA 조세막조직중 FOXP3표체수평명현저우정상대조조(P <0.01)。BSP 현시 URSA 조 FOXP3기인계동자갑기화수평명현고우정상대조조(P <0.01)。FOXP3단백표체수평여 FOXP3기인계동자갑기화수평정부상관(r =-0.917,P <0.01)。결론FOXP3기인계동자갑기화수평승고후,FOXP3기인단백표체수평하조,인기면역내수이상,가능도치 RSA 적발병。
Objective To investigate the association between the level of FOXP3 promoter methyla-tion and the expression level of FOXP3 protein in the decidua of patients with unexplained recurrent spontane-ous abortion (URSA).Methods The expression levels of FOXP3 protein in the decidua of 20 URSA patients and 20 healthy counterparts who underwent induced abortion were assessed by Western blot.Bisulfite-assisted genomic sequencing PCR (BSP)was utilized to detect the levels of FOXP3 promoter methylation.The correla-tion between two indexes was evaluated.Results The expression level of FOXP3 in the decidua of the URSA group was significantly lower than that of the control group (P <0.01),whereas the level of FOXP3 promoter methylation in the URSA group was significantly higher compared with that in the control group (P <0.01).The expression level of FOXP3 protein was negatively correlated with the level of FOXP3 promoter methylation (r =-0.917,P <0.01).Conclusion As the level of FOXP3 promoter methylation increases,the expres-sion level of FOXP3 protein is down-regulated,which may cause abnormal immune tolerance and potentially lead to the incidence of RSA.