摘要
目的探究T细胞免疫球蛋白粘蛋白分子3(Tim-3)表达异常与不明原因复发性流产(URSA)的关系。方法选择31例URSA患者作为研究组,并以同期30例正常孕妇作为对照组。采用流式细胞术检测两组外周血单个核细胞(PBMC)中CD4+Tim-3+细胞/CD4+细胞的比例,Western Blot技术检测蜕膜中Tim-3蛋白的相对含量,并以免疫磁珠法分选CD4+Tim-3+细胞,荧光定量RT-PCR检测两组外周血PBMC、CD4+Tim-3+细胞及蜕膜组织中Tim-3 mRNA的表达。结果 URSA组中,PBMC中CD4+Tim-3+细胞/CD4+细胞为5.23±0.96%,蜕膜中Tim-3蛋白的相对表达量为0.64±0.09,PBMC及蜕膜中Tim-3 mRNA的相对表达量为0.65±0.09及0.50±0.07,均显著高于正常对照组(P<0.01)。但是,URSA组CD4+Tim-3+细胞(Th1细胞)Tim-3 mRNA的表达量低于正常对照组,差异具有显著性(P<0.01)。结论 Th1细胞Tim-3表达降低,Th1细胞过度活化可能参与了URSA的发生发展过程。
Objective: To explore the relationship between abnormal expression of T eel] immunoglobulin - and muein - domain containing molecular- 3 (Tim- 3 ) and unexplained recurrent spontaneous abortion (URSA). Methods: 31 pregnant women suffered with URSA were recruited as the study group and 30 normal pregnant women were chosen as the control group. For the two groups, CD4^± Tim - 3 ^± cells/CD4 ^± cell percentage in peripheral blood mononuelear ( PBMC ) were detected by flow eytometry. Then CD4^± Tim - 3^± ceils were collected by magnetic activated cell sorting. The expression levels of Tim - 3 mRNA in PBMC, CD4 ^± Tim - 3 ^± cells and decidua were detected by fluorescent quantitative RT - PCR. Besides, the relative amount of Tim - 3 protein was also analyzed using Western blot. Results : In URSA group, the CD4 ^± Tim - 3 ^± cells/CD4^± cell percentage in PBMC was 5.23 ± 0. 96% , the relative level of Tim - 3 protein in decidua was 0. 64 ± 0. 09, the relative amounts of Tim - 3 mRNA in PBMC and decidua were 0. 65 ± 0. 09 and 0. 50 ± 0. 07 respectively, which were all significantly higher that those in the control group. However, the expression of Tim - 3 mRNA by CD4^± Tim -3^± ceils (Thl cells) in the URSA group was statistically lower than that in normal control. Conclusion: Down - regulation of Tim - 3 on Thl cells and excessive activation of Thl might contribute to the development of URSA.
出处
《中国优生与遗传杂志》
2012年第2期31-34,共4页
Chinese Journal of Birth Health & Heredity
基金
教育部高等学校博士学科点专项科研基金资助课题(200804861049)
湖北省自然科学基金计划重点项目(2008CDA008)