期刊文献+

CCAAT/增强子结合蛋白β在系统性红斑狼疮患者外周血单个核细胞中的表达及意义

The expression and significance of CCAAT/enhancer binding proteins β in peripheral blood mononuclear cell of systemic lupus erythematosus
下载PDF
导出
摘要 目的探讨系统性红斑狼疮(systemic lupus erythematosus,SLE)患者外周血单个核细胞(peripheral blood mononuclear cell,PBMC)中CCAAT/增强子结合蛋白(CCAAT/enhancer binding proteinsβ,C/EBPβ)的表达及其意义。方法从SLE患者血液中分离血浆和PBMC。通过定量PCR(quantitative PCR,q PCR)和Western blot方法检测SLE患者和健康对照PBMC中C/EBPβm RNA及其功能活性形式LAP(liver-enriched activating protein)蛋白表达水平。诱导THP-1细胞成为单核巨噬细胞,再分别用SLE患者血浆和健康对照血浆刺激24 h后,通过q PCR和Western blot方法检测C/EBPβm RNA和LAP蛋白表达水平。结果 SLE患者外周血PBMC中C/EBPβm RNA及LAP蛋白水平高于正常对照(P<0.05)。SLE患者外周血PBMC中C/EBPβm RNA表达水平及LAP蛋白灰度值与SLE疾病严重程度评分(SLEDAI评分)正相关(P<0.05,r>0)。与正常对照血浆相比,SLE患者血浆刺激THP-1细胞诱导成的单核巨噬细胞24 h后C/EBPβm RNA和LAP蛋白水平显著升高(P<0.05)。结论 SLE患者外周血PBMC中C/EBPβ表达显著升高,尤其是在单核巨噬细胞中,提示C/EBPβ表达升高参与SLE炎症发生的过程。 This study designed to explore the expression and significance of CCAAT/enhancer binding proteinsβ(C/EBPβ) in peripheral blood mononuclear cell(PBMC) of systemic lupus erythematosus(SLE). Quantitative PCR(q PCR) and Western blot were used to observe C/EBPβ m RNA and LAP(liver-enriched activating protein)expression in peripheral blood mononuclear cell of SLE patient and healthy control. SLE patient plasma and healthy control plasma were used to stimulate the THP-1 derived monocyte-macrophage for 24 h. Then q PCR and Western blot were used to observe the m RNA and LAP protein expression of C/EBPβ. The difference was analyzed by the Mann-Whitney test; correlation analyses were conducted using Spearman's rank test. Results indicated that C/EBPβ m RNA and LAP protein expression in SLE patient PBMC were increased(P〈 0.05). C/EBPβ m RNA expression level and LAP protein gray level positively correlated with SLEDAI(P 〈0.05,r〉 0). SLE patient plasma stimulation upregulated C/EBPβ m RNA and LAP protein expression in THP-1 derived monocyte-macrophage(P〈 0.05). In conclusion, the change of C/EBPβ expression, especially in monocyte-macrophage, contributes to the pathogenesis of SLE disease.
出处 《免疫学杂志》 CAS CSCD 北大核心 2015年第4期336-339,344,共5页 Immunological Journal
基金 国家自然科学基金(81201232 81271753)
关键词 系统性红斑狼疮 CCAAT/增强子结合蛋白 单核巨噬细胞 Systemic lupus erythematosus CCAAT/enhancer binding proteins β Monocyte-macrophage
  • 相关文献

参考文献20

  • 1Sears RC, Sealy L. Multiple fonns of ClEBP beta bind the EFII enhancer sequence in the Rous sarcoma virus long terminal repeat[J]. Mol Cell Bioi, 1994, 14(7): 4855-4871.
  • 2Williams SC, Baer M, Dillner AJ, et a1. CRP2 (ClEBP beta) contains a bipartite regulatory domain that controls transcriptional activation, DNA binding and cell specificity[J]. EMBO J, 1995,14(13): 3170-3183.
  • 3Huber R, Pietsch D, Panterodt T, et at. Regulation of CJ EBPbeta and resulting functions in cells of the monocytic lineage[J]. Cell Signal, 2012, 24(6): 1287-1296.
  • 4Zhou J, Wu R, High AA, et at. A20-binding inhibitor of NF-kappaB (ABINI) controls Toll-like receptor-mediated CCAAT/enhancer -binding protein beta activation and protects from inflammatory disease[J]. Proc Natl Acad Sci USA, 2011, 108(44): E998-1006.
  • 5Fojtikova M, Cerna M, Pavelka K. A review of the effects of prolactin hormone and cytokine on the development and pathogenesis of autoimmune diseases[J]. Vnitr Lek, 2010, 56(5): 402-413.
  • 6Peng H, Wang W, Zhou M, et al. Role of interleukin-IO and interleukin -10 receptor in systemic lupus erythematosus[J]. Clin Rheumatol, 2013, 32(9): 1255-1266.
  • 7Flesher DL, Sun X, Behrens TW, et at. Recent advances in the genetics of systemic lupus erythematosus[J]. Expert Rev Clin Immunol, 2010, 6(3): 461-479.
  • 8Guiducci C, Gong M, Xu Z, et al. TLR recognition of self nucleic acids hampers glucocorticoid activity in lupus[J]. Nature, 2010, 465(7300): 937-941.
  • 9Lande R, Gregorio J, Facchinetti V, et al. Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide[J]. Nature, 2007, 449(7162): 564-569.
  • 10Diebold SS, Massacrier C, Akira S, et al. Nucleic acid agonists for Toll -like receptor 7 are defined by the presence of uridine ribonucleotides[J]. Eur J Immunol, 2006, 36(12): 3256-3267.

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