期刊文献+

原因不明复发性流产患者蜕膜Foxp3 mRNA及蛋白质的表达 被引量:6

Expressions of Foxp3 mRNA and protein in decidua of women with unexplained recurrent spontaneous abortion.
下载PDF
导出
摘要 目的:探讨原因不明复发性流产(URSA)患者蜕膜Foxp3 mRNA及蛋白的表达。方法:分别采用免疫组化S-P法、半定量和实时定量PCR法和W estern B lot法检测25例URSA患者蜕膜组织Foxp3 mRNA及蛋白的表达与分布,并以32例正常早孕妇女为对照。结果:(1)免疫组化S-P法显示Foxp3表达于胞浆,妊娠后的蜕膜组织有Foxp3的表达;URSA患者蜕膜Foxp3的表达显著低于正常妊娠妇女(P<0.01);(2)半定量和实时定量RT-PCR法分析均显示,URSA患者蜕膜组织Foxp3 mRNA的表达显著低于正常早孕妇女(P<0.05);(3)W estern B lot法分析显示,URSA患者蜕膜组织Foxp3蛋白的表达显著低于正常早孕妇女(P<0.05)。结论:Foxp3可能在维持早期妊娠中起重要作用,其表达水平降低可能与URSA的发病有关。 Objective:To observe the expression of Foxp3 mRNA and protein in human decidua of normal pregnant women(NP) and patients with unexplained recurrent spontaneous abortion(URSA). Method:Expression and distribution of Foxp3 in decidua of 32cases of NP women and 25 cases of URSA patients were observed respectively by immunohistochemistry, semi-quantitative RT-PCR, real-time PCR and Western blotting. Results: ( 1 ) By immunohisto- chemistry, the expression of Foxp3 was observed to be localized in the cytoplasm of pregnancy decidua. Foxp3 expression in URSA patients was lower significantly compared with NP women ( P 〈0. O1 ) ; (2) Expression of Foxp3 mRNA in deciduas of URSA was significantly lower compared with NP women by semi-quantitative RT-PCR and real-time PCR ( P 〈0. 01 ) ; ( 3 ) Expression of Foxp3 protein in deciduas of URSA patients was significantly lower than those of NP women by Western blotting analysis ( P 〈0. 05 ). Conclusion: The expression of Foxp3 would be an important factor related with the maintenance of pregnancy. The lower expression of Foxp3 in URSA is involved in the pathogenesis of URSA.
出处 《现代妇产科进展》 CSCD 北大核心 2006年第4期292-294,F0003,共4页 Progress in Obstetrics and Gynecology
关键词 流产 复发性 蜕膜 调节性T细胞 Abortion, recurrent Decidua Regulatory T cell
  • 相关文献

参考文献8

  • 1林其德.原因不明复发性流产的基础与临床研究进展[J].中华妇产科杂志,2003,38(8):481-483. 被引量:156
  • 2Stephens LA,Mottet C,Mason D,et al.Human CD4 (+)CD25 (+) thymocytes and peripheral T cells have immune suppressive activity in vitro[J].Eur J Immunol,2001,31:1247-1254
  • 3Aluvihare VR,Kallikourdis M,Betz AG.Tolerance,suppression and the fetal allograft[J].J Mol Med,2005,83:88-96
  • 4Hori S,Nomura T,Sakaguchi S.Control of regulatory T cell development by the transcription factor Foxp3[J].Science,2003,299:1057-1061
  • 5Wang XP,Ma ZW,Hong Y,et al.The skewed TCR-BV repertoire displayed at the maternal-fetal interface of women with unexplained pregnancy loss[J].Am Journal of Reproduc Immunolo,2005,54:1-12
  • 6Sakaguchi S,Sakaguchi N,Asano M,et al.Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25).Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases[J].J Immunol,1995,155:1151-1164
  • 7邱丽华,林其德.调节性T淋巴细胞与原因不明复发性流产的相关性研究[J].中华妇产科杂志,2004,39(12):816-818. 被引量:48
  • 8Fontenot JD,Gavin MA,Rudensky AY.Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells[J].Nat Immunol,2003,4:330-336

二级参考文献7

  • 1Suto A, Nakajima H, Kagami SI, et al. Role of CD4(+) CD25(+) regulatory T cells in T helper 2 cell-mediated allergic inflammation in the airways.Am J Respir Crit Care Med, 2001,164:680-687.
  • 2Sakaguchi S, Sakaguchi N, Asano M, et al. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases.J Immunol, 1995,155:115
  • 3Stephens LA, Mottet C, Mason D, et al. Human CD4(+)CD25(+) thymocytes and peripheral T cells have immune suppressive activity in vitro.Eur J Immunol, 2001,31:1247-1254.
  • 4Levings MK, Sangregorio R, Roncarolo MG. Human cd25(+)cd4(+) t regulatory cells suppress naive and memory T cell proliferation and can be expanded in vitro without loss of function.J Exp Med, 2001,193:1295-1302.
  • 5Taylor PA, Lees CJ, Blazar BR. The infusion of ex vivo activated and expanded CD4(+)CD25(+) immune regulatory cells inhibits graft-versus-host disease lethality.Blood, 2002,99:3493-3499.
  • 6Sasada T, Kimura M, Yoshida Y, et al. CD4+CD25+ regulatory T cells in patients with gastrointestinal malignancies: possible involvement of regulatory T cells in disease progression.Cancer, 2003,98:1089-1099.
  • 7Kohm AP, Carpentier PA, Anger HA, et al. Cutting edge: CD4+CD25+ regulatory T cells suppress antigen-specific autoreactive immune responses and central nervous system inflammation during active experimental autoimmune encephalomyelitis.J Immunol, 2002,169

共引文献194

同被引文献68

引证文献6

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部