期刊文献+

女性类风湿关节炎患者miR-146a、miR-23b的表达及雌激素对其的影响 被引量:8

Expression of miR-146a and miR-23b in peripheral blood mononuclear cells in female patients with rheumatoid arthritis and the effects of estrogen on them
在线阅读 下载PDF
导出
摘要 目的:比较女性类风湿关节炎(RA)患者miR-146a、miR-23b的表达水平与健康者的差异,分析miRNAs与炎症因子IL-17及实验室指标的相关性,以明确miR-146a、miR-23b是否与RA相关;分析雌激素对miR-146a、miR-23b及IL-17表达的影响,以明确雌激素影响RA的可能机制。方法:实时荧光定量PCR检测27例女性RA患者及27名女性健康体检者PBMCs中miR-146a、miR-23b的表达水平,酶联免疫吸附实验(ELISA)检测血浆IL-17的浓度,统计分析RA患者miR-146a、miR-23b及IL-17的表达水平与健康者的差异;收集RA患者临床实验室指标ESR、CRP、抗CCP抗体、RF的检测结果,计算DAS28评分,分析miR-146a、miR-23b分别与血浆IL-17、ESR、CRP、抗CCP抗体、RF及DAS28的相关性。再用雌二醇处理RA组和对照组的PBMCs后同样检测miR-146a、miR-23b及培养上清IL-17的水平,分析雌激素处理前后其水平变化。结果:女性RA患者PBMCs中miR-146a、miR-23b显著高于健康对照(P<0.05),miR-146a、miR-23b的表达水平分别与血浆IL-17、ESR、血清CRP、抗CCP抗体、RF、DAS28之间均无显著相关性(P>0.05)。经雌二醇处理后,女性RA患者PBMCs中miR-146a、miR-23b无显著变化(P>0.05),培养上清IL-17浓度显著增高(P<0.05),健康体检者PBMCs中miR-146a的表达水平明显下调(P<0.05),miR-23b的表达水平无明显变化(P>0.05)。结论:女性RA患者PBMCs中miR-146a、miR-23b的表达水平显著上调。雌激素可能一方面通过增强IL-17的表达参与RA的病程,另一方面通过下调PBMCs中miR-146a的表达阻止健康人向RA发展。 Objective:To compare the expression levels of miR-146a and miR-23b in female patients with rheumatoid arthritis(RA)and healthy people,and analyze the correlation between miRNAs and inflammatory factors IL-17 and laboratory indicators,so as to clarify whether miR-146a and miR-23b are related to RA,to analyze the effect of estrogen on the expression of miR-146a,miR-23b and IL-17,so as to clarify the possible mechanism of estrogen affecting RA.Methods:The expression levels of miR-146a and miR-23b were measured by RT-qPCR in 27 female RA patients and 27 female healthy individuals,and the concentration of IL-17 in plasma and culture supernatant was measured by ELISA.The difference of expression level of miR-146a、miR-23b and IL-17 in RA patients and healthy individuals was analyzed.Collected the clinical laboratory indexes of RA patients including ESR,CRP,anti CCP antibody,RF and calculating the score of DAS28,the correlation between miR-146a and miR-23b with IL-17,ESR,CRP,anti CCP antibodies,RF and DAS28 were analyzed,respectively.In addition,the levels of miR-146a,miR-23b and IL-17 were also detected after PBMCs treatment by estradiol between RA group and control group,and the differences were analyzed.Results:The expression levels of miR-146a and miR-23b in female RA patients increased compared to those in the healthy individuals(P<0.05).There was no significant correlation between miR-146a or miR-23b with IL-17,ESR,CRP,anti CCP antibody,RF and DAS28(P>0.05).After estrogen treatment,there was no significant change in miR-146a and miR-23b in female RA patients,the concentration of IL-17 in supernatant in female RA patients was significantly increased(P<0.05),and the expression level of miR-146a in healthy individuals was significantly down-regulated(P<0.05),the expression level of miR-23b did not change significantly(P>0.05).Conclusion:The expression levels of miR-146a and miR-23b in female RA patients are up-regulated.Estrogen may to be involved in the developement of RA by up-regulation IL-17.On the other hand,estrogen may prevent healthy people from developing to RA by down-regulation of miR-146a in the PBMCs in healthy individuals.
作者 祝静 晏波 蒋瑶 王东生 邢艳 ZHU Jing;YAN Bo;JIANG Yao;WANG Dong-sheng;XING Yan(Department of Laboratory Medicine,North Sichuan Medical College;Department of Clinical Laboratory,Affiliated Hospital of North Sichuan Medical College;Transforming Medicine Research Centre,North Sichuan Medical College,Nanchong 637000;Department of Laboratory,Sichuan Cancer Hospital,Chengdu 610000,Sichuan,China)
出处 《川北医学院学报》 CAS 2020年第4期637-641,共5页 Journal of North Sichuan Medical College
基金 四川省学术和技术带头人培养基金(740/74130801)。
关键词 类风湿关节炎 雌激素 MIR-146A miR-23b 白细胞介素-17 Rheumatoid arthritis Estrogen miR-146a miR-23b IL-17
  • 相关文献

参考文献5

二级参考文献67

  • 1汪理,林星光,金昊,童荔,陈忠华,昌盛.妊娠浓度的雌激素对诱导CD4^+CD25^-naive T细胞转化为CD4^+CD25^+Treg细胞的影响[J].免疫学杂志,2009,25(1):61-63. 被引量:9
  • 2Kawashima M, Miossec P. mRNA quantification of T-bet, GATA-3, IFN-gamma, and IL-4 shows a defective Thl immune response in the peripheral blood from rheumatoid arthritis patients: link with disease activity [J]. J Clin Immunol, 2005, 25 (3): 209-214.
  • 3Nanki T. Molecular mechanisms of bone destruction in rheumatoid arthritis [J]. Clin Calcium, 2007, 17 (4): 510-516.
  • 4Garcia Vicuna R, Gomez Gaviro MV, Dominguez Luis MJ, et al. CC and CXC chemokine receptors mediate migration, proliferation, and matrix metalloproteinase production by fibroblast-like synoviocytes from rheumatoid arthritis patients [J]. Arthritis Rheum, 2004, 50 (12): 3866-3877.
  • 5Cutolo M, Seriolo B, Villaggio B, et al. Androgens and estrogens modulate the immune and inflammatory responses in rheumatoid arthritis [J]. Ann N Y Acad Sci, 2002, 966: 131-142.
  • 6Schmidt M, Hartung R, Capellino S, et al. Estrone/17beta-estradiol conversion to, and tumor necrosis factor inhibition by, estrogen metabolites in synovial cells of patients with rheumatoid arthritis and patients with osteoarthritis [J]. Arthritis Rheum, 2009, 60 (10): 2913-2922.
  • 7Gonz a lez Canga A, Ugai K, Suzuki M, et al. Association of cytosine-adenine repeat polymorphism of the estrogen receptor-beta gene with rheumatoid arthritis symptoms [J]. Rheumatol Int, 2010, 30 (9): 1259-1262.
  • 8Capellino S, Montagna P, Villaggio B, et al. Hydroxylated estrogen metabolites influence the proliferation of cultured human monocytes: possible role in synovial tissue hyperpla- sia [J]. Chn Exp Rheumatol, 2008, 26 (5): 903-909.
  • 9Khalkhali Ellis Z, Seftor EA, Nieva DR, et al. Estrogen and progesterone regulation of human fibroblast-like synoviocyte function in vitro: implications in rheumatoid arthritis [J]. J Rheumatol, 2000, 27 (7): 1622-1631.
  • 10Itoh Y, Hayashi H, Miyazawa K, et al. 17beta-estradiol induces IL-1 {alpha} gene expression in rheumatoid fibrob- last-hke synovial cells through estrogen receptor {alpha} (ER {alpha}) and augmentation of transcriptional activity of spl by dissociating histone deacetylase 2 from ER {alpha} [J]. J Immunol, 2007, 178 (5): 3059-3066.

共引文献38

同被引文献126

引证文献8

二级引证文献17

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