期刊文献+

Foxo1-KLF2-S1P1在MG患者胸腺组织的表达 被引量:2

The pilot study of Foxo1-KLF2-S1P1 in the thymus of patients with myasthenia gravis
下载PDF
导出
摘要 目的通过探讨Foxo1-KLF2-S1P1在MG患者胸腺的表达,分析其对胸腺T细胞输出的影响。方法取MG患者及对照组胸腺组织,提取总RNA,通过荧光定量RT-PCR检测Foxo1、KLF2、S1P1及CD62L、CCR7、CD69的表达;制作胸腺组织切片,通过免疫组化了解Foxo1、S1P1、CD62L、CD69、CCR7在胸腺组织的分布与表达。结果免疫组化显示Foxo1、S1P1、CCR7在MG患者及对照组胸腺都有表达,主要分布在髓质区,MG患者胸腺组织髓质区扩大,Foxo1、S1P1、CCR7表达显著高于对照组;荧光定量PCR结果显示MG胸腺组织Foxo1、KLF2、S1P1、CCR7、CD69的m RNA的水平表达显著增高(分别是5.36±0.728、1.43±2.71、6.1±1.033、5.0±0.932、4.97±1.112,与对照组相比P<0.05)。结论 MG患者Foxo1-KLF2-S1P1高表达可能是MG患者胸腺细胞的异常输出的原因。 This study aims to explore the roles of Foxo1-KLF2 and S1P1 in T cells output of myasthenia gravis (MG) thymus by analyzing the expression of Foxo1-KLF2 and S1P1 in thymus of klG patients. Total RNA extracted from the thymus tissue of MG patients and control people were collected, then the mRNA expression levels of Foxol, KLF2, S1P1, CD62L, CCR7, and CD69 were examined by real-time PCR. At the same time, Paraffin-embedded sections of thymus from MG patients and control people were made and stained with HE, then the protein expression and distribution of Foxo1, S1P1, CD62L, CCR7, and CD69 were checked by immunohistochemistry method in these Paraffin-embedded sections. The results of real-time PCR showed that the mRNA expression of Foxo1, KLF2, S1P1, CCR7, and CD69 in thymus tissue of MG increased significantly as compared with those in thymus tissue of control people (P〈 0.05); the results of immunohistochemistry showed that although Foxol, S1P1 and CCR7, mainly distributed in the medulla area in thymus, expressed not only in the thymus tissue of MG patients but also control people, the medulla area of thymus tissue in MG patient was expanded than that in control people, and the protein expressions of Foxo1, S1P1 and CCR7 were significantly higher in thymus tissue from MG patients than those from control people (P〈 0.05). Taken together, high expression of Foxo1-KLF2-S1P1 in thymus could be the major reason for unusual output of T cells in MG patients.
出处 《免疫学杂志》 CAS CSCD 北大核心 2015年第2期181-184,共4页 Immunological Journal
基金 国家自然科学基金(81471545 81172874)
关键词 重症肌无力 胸腺 FOXO1 KLF2 S1P1 Myasthenia gravis Thymus T cell Foxo1 KLF2 S1P1
  • 相关文献

参考文献20

  • 1Utsugisawa K, Nagane Y, Suzuki S, et al. Antigen rspecific Tr cell acrtivation in hyperplastic thymus in myasthenia gravis[J]. Muscle Nerve, 2007, 36(1) : 100-103. 被引量:1
  • 2Allende ML, Dreier JL, Mandala S, et al. Expression of the sphingosine 1-phosphate receptor, S1P1, on T-cells controls thymic emigration[J]. J Biol Chem, 2004, 279(15): 15396-15401. 被引量:1
  • 3Matloubian M, Lo CG, Cinamon G, et aL Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on SIP receptor 1 [J]. Nature, 2004, 427(6972): 355-360. 被引量:1
  • 4Zachariah MA, Cyster JG. Neural crest-derived pericytes promote egress of mature thymocytes at the cortieomedullary junction [J]. Science, 2010, 328 (5982): 1129-1135. 被引量:1
  • 5Pappu R, Schwab SR, Cornelissen L, et al. Promotion of lymphocyte egress into blood and lymph by distinct sources of sphingosine-l-phosphate[J]. Science, 2007, 316(5822): 295-298. 被引量:1
  • 6Carlson CM, Endrizzi BT, Wu J, et al, Kruppel-like factor 2 regulates thymocyte and T-cell migration[J]. Nature, 2006, 442(7100):299-302. 被引量:1
  • 7Fabre S, Carrette F, Chen J, et al. FOXO1 regulates L- Seleetin and a network of human T cell homing molecules Downstream of phosphatidylinositol 3 -kinase [J]. J Immunol, 2008, 181(5):2980-2989. 被引量:1
  • 8Kerdiles YM, Beisner DR, Tinoco R, et al. Foxol linkshoming and survival of naive T cells by regulating L- selectin, CCR7 and interleukin 7 receptor[J]. Nat Immunol, 2009, 10(2): 176-184. 被引量:1
  • 9Gubbels Bupp MR, Edwards B, Guo C, et al. T cells require Foxol to populate the peripheral lymphoid organs[J]. Eur J Immunol, 2009, 39(11): 2991-2999. 被引量:1
  • 10Ouyang W, Beckett O, Flavell RA, et al. An essential role of the Forkhead-box transcription factor Foxol in control of T cell homeostasis and tolerance[J], Immunity, 2009, 30(3): 358-371. 被引量:1

二级参考文献37

  • 1Yang W, Lu J, Weng J, et al. Prevalence of diabetes among men and women in China [J]. N Engl J Med, 2010, 362 (12): 1090-1101. 被引量:1
  • 2Butler AE, Janson J, Bonner Weir S, et al. Beta-cell deficit and increased beta-cell apoptosis in humans with type 2 diabetes [J]. Diabetes, 2003, 52 (1):102-110. 被引量:1
  • 3Maiese K, Hou J, Chong ZZ, et al. A fork in the path: Developing therapeutic inroads with FoxO proteins [J].Oxid Med Cell Longev, 2009, 2 (3): 119-129. 被引量:1
  • 4Marette A. Mediators of cytokine-induccd insulin resistance in obesity and other inflammatory settings [J].Curr Opin Clin Nutr Metab Care, 2002, 5 (4): 377-383. 被引量:1
  • 5Guest CB, Park MJ, Johnson DR, et al. The implication of proinflammatory cytokines in type 2 diabetes [J]. Front Biosci, 2008, 13: 5187-5194. 被引量:1
  • 6Dandona P, Aljada A, Bandyopadhyay A. Inflammation: the link between insulin resistance, obesity and diabetes [J]. Trends Immunol, 2004, 25 (1): 4-7. 被引量:1
  • 7Tilg H, Moschen AR. Inflammatory mechanisms in the regulation of insulin resistance [J]. Mol Med, 2008, 14 (3/4): 222-231. 被引量:1
  • 8Su D, Coudriet GM, Hyun Kim D, et al. FoxO1 links insulin resistance to proinflammatory cytokine IL-lbeta production in macrophages[J]. Diabetes, 2009, 58 (11): 2624-2633. 被引量:1
  • 9Kayal RA, Siqueira M, Alhlowi J, et al. TNF-alpha mediates diabetes-enhanced chondrocyte apoptosis during fracture healing and stimulates chondrocyte apoptosis through FOX- O1[J]. J Bone Miner Res, 2010, 25 (7): 1604-1615. 被引量:1
  • 10Larsen CM, Faulenbach M, Vaag A, et al. Interleukin-1-receptor antagonist in type 2 diabetes mellitus [J]. N Engl J Med, 2007, 356 (15): 1517-1526. 被引量:1

共引文献14

同被引文献6

引证文献2

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