中国综合临床
中國綜閤臨床
중국종합림상
CLINICAL MEDICINE OF CHINA
2011年
12期
1266-1268
,共3页
谢小花%于晓红%曾慧红%张晓玲
謝小花%于曉紅%曾慧紅%張曉玲
사소화%우효홍%증혜홍%장효령
子宫内膜异位症%巨噬细胞移动抑制因子%免疫%血管生成
子宮內膜異位癥%巨噬細胞移動抑製因子%免疫%血管生成
자궁내막이위증%거서세포이동억제인자%면역%혈관생성
Ovarian Endometriosis%Macrophage migration inhibitory factor%Immune%Angiogenesis
目的 探讨巨噬细胞移动抑制因子(MIF)在卵巢子宫内膜异位症(OEms)组织中表达的意义.方法 应用ElivisionTm plus免疫组化方法检测30例OEms异位、在位内膜和非子宫内膜异位症(Ems)子宫内膜组织(对照组)中的MIF,并应用计算机图像分析系统对结果进行体视学指标平均吸光度的检测.结果 OEms组异位内膜、在位内膜及对照组中MIF的吸光度分别为(0.180±0.013)、(0.158 ±0.022)及(0.143±0.029),3组间比较,差异有统计学意义(F =47.676,P<0.001).MIF蛋白在OEms组在位内膜增生期和分泌期的表达均高于对照组同期水平(0.157±0.018与0.146±0.029,t=2.656,P=0.009;0.160 ±0.028与0.137±0.030,t=3.059,P=0.003).结论 MIF可能在Ems的发生、发展过程中起重要作用.
目的 探討巨噬細胞移動抑製因子(MIF)在卵巢子宮內膜異位癥(OEms)組織中錶達的意義.方法 應用ElivisionTm plus免疫組化方法檢測30例OEms異位、在位內膜和非子宮內膜異位癥(Ems)子宮內膜組織(對照組)中的MIF,併應用計算機圖像分析繫統對結果進行體視學指標平均吸光度的檢測.結果 OEms組異位內膜、在位內膜及對照組中MIF的吸光度分彆為(0.180±0.013)、(0.158 ±0.022)及(0.143±0.029),3組間比較,差異有統計學意義(F =47.676,P<0.001).MIF蛋白在OEms組在位內膜增生期和分泌期的錶達均高于對照組同期水平(0.157±0.018與0.146±0.029,t=2.656,P=0.009;0.160 ±0.028與0.137±0.030,t=3.059,P=0.003).結論 MIF可能在Ems的髮生、髮展過程中起重要作用.
목적 탐토거서세포이동억제인자(MIF)재란소자궁내막이위증(OEms)조직중표체적의의.방법 응용ElivisionTm plus면역조화방법검측30례OEms이위、재위내막화비자궁내막이위증(Ems)자궁내막조직(대조조)중적MIF,병응용계산궤도상분석계통대결과진행체시학지표평균흡광도적검측.결과 OEms조이위내막、재위내막급대조조중MIF적흡광도분별위(0.180±0.013)、(0.158 ±0.022)급(0.143±0.029),3조간비교,차이유통계학의의(F =47.676,P<0.001).MIF단백재OEms조재위내막증생기화분비기적표체균고우대조조동기수평(0.157±0.018여0.146±0.029,t=2.656,P=0.009;0.160 ±0.028여0.137±0.030,t=3.059,P=0.003).결론 MIF가능재Ems적발생、발전과정중기중요작용.
Objective To investigate the significance of macrophage migration inhibitory factor(MIF) in ovarian endometriosis (OEms).Methods MIF of ectopic endometriumeutopic endometrium in OEms and endometrium in non-endometriosis (30 cases in every group ) was detected by Elivision TM plus immunohistochemical.Quantitative images analytical system was performed with computer to analyze the mean absorbance(A) of MIF.Results The A of MIF in ectopic and eutopic endometrium of OEms and the normal control was respectively ( 0.180 ± 0.013 ),( 0.158 ± 0.022 ) and ( 0.143 ± 0.029 ),there was statistical significance between groups ( F =47.676,P < 0.001 ).The expression of MIF in proliferative phase of eutopic endometrium of OEms was(0.157 ±0.018),extremely stronger than that in the same phase of the normal control (0.146 ± 0.029 ) ( t =2.656,P =0.009 ) ; and MIF in secretory phase of eutopic endometrium of OEms was (0.160±0.028),obviously higher than that in the same phase of the normal control(0.137 ±0.030) (t =3.059,P =0.003).Conclusion The MIF may play a significant role in the pathogenesis and development of ovarian endometriosis.