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miR-92a-3p对TNF-α,IL-6和DcR3的影响 被引量:1

Effects of miRNA-92a-3p on TNF-α,IL-6 and DcR3
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摘要 目的探讨miR-92a-3p对肿瘤坏死因子-α(TNF-α),白细胞介素-6(IL-6)和诱导因子3(DcR3)的影响。方法用人急性单核细胞白血病细胞(THP-1)设置阴性对照组(NC)。用1μg/mL LPS分别处理THP-1细胞6 h和24 h,实时荧光定量聚合酶链反应(q-PCR)检测TNF-α,IL-6和DcR3的表达,作为Sepsis组(NC+LPS)。利用1μg/mL的LPS处理过表达miR-92a-3p的THP-1细胞,作为过表达miR-92a-3p的Sepsis组(miR-92a-3p+LPS)。利用q-PCR,酶联免疫吸附试验(ELISA)和Western blot分别检测各组TNF-α,IL-6和DcR3的表达情况。结果q-PCR,ELISA和Western blot检测结果显示,TNF-α和IL-6在LPS组、miR-92a-3p+LPS组和NC组的相对表达量均呈下调趋势,差异有统计学意义(P<0.05),DcR3表达差异无统计学意义(P>0.05)。结论miR-92a-3p可抑制TNF-α和IL-6的释放,具有抗炎作用,但是其对DcR3的作用不显著。 Objective To investigate the effects of miRNA-92a-3p on tumor necrosis factor-alpha(TNF-α),interleukin-6(IL-6)and decoy factor-3(DcR3).Methods Human acute mononuclear leukemia cells(THP-1)were used as negative control group(NC).THP-1 cells were treated with 1μg/mL LPS for 6 h and 24 h,respectively.The expression of TNF-a,IL-6 and DcR3 was detected by q-PCR as Sepsis group(NC+LPS).THP-1 cells overexpressing miRNA-92a-3p were treated with 1μg/mL LPS as sepsis group overexpressing miRNA-92a-3p(miRNA-92a-3p+LPS).The expression of TNF-α,IL-6 and DcR3 was detected by q-PCR,ELISA and Western blot.Results The results of q-PCR,ELISA and Western blot showed that the relative expression of TNF-αand IL-6 in LPS group,Mi-92a-3p+LPS group and NC group decreased(P<0.05),while the expression of DcR3 had no statistical significance(P>0.05).Conclusion MiR-92a-3p can inhibit the release of TNF-αand IL-6,and has anti-inflammatory effect,but its effect on DcR3 is not significant.
作者 陈洪卫 娄晓丽 赵静静 侯彦强 CHEN Hongwei;LOU Xiaoli;ZHAO Jingjing;HOU Yanqiang(Department of Clinical Laboratory,Shanghai Songjiang District Central Hospital,Shanghai 201600,China)
出处 《国际检验医学杂志》 CAS 2019年第20期2444-2448,共5页 International Journal of Laboratory Medicine
基金 上海市卫健委青年科研项目(20164y0025) 上海市松江区科学技术攻关项目(2017sjkjgg48)
关键词 脓毒症 miR-92a-3p 肿瘤坏死因子-Α 白细胞介素-6 诱导因子3 sepsis miRNA-92a-3p tumor necrosis factor-alpha interleukin-6 decoy factor 3
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  • 1Prucha M, Bellingan G, Zazula R. Sepsis biomarkers [J]Clin Chim Aela, 2015, 440:97-103.
  • 2Dellinger RP, Levy MM, Ri~odes A, et al. Surviving sepsis campaign: international guidelines for managemenl of severe sepsis and septic shock: 2012 [J]. Crit Care Meal,2013,41 (2) : 580-637.
  • 3Wang Z, Ruan Z, Mao Y, et al. miR-27a is up regulated and promotes inflammatory response in sepsis [Jl. Cell Immunol, 2014, 290(2) : 190-195.
  • 4Wang HJ, Deng J, Wang JY, et al. Serum miRi 122 levels are related to coagulation disorders in sepsis patients ~J]. Clin Chem Lab Med, 2014, 52 (6) : 927 -933.
  • 5Tacke F, Roderburg C, Benz F, et al. Levels of circulating miR- 133a are elevated in sepsis and predict mortality in critically ill patients [J]. Crit Care Med, 2014, 42 (5) : 1096-1104.
  • 6Wu SC, Yang JC, Rau CS, et al. Profiling circulating microRNA expression in experimental sepsis using cecal ligation and puncture [J]. PLoS One, 2013, 8 (10) : e77936.
  • 7Hsieh CI-I, Rau CS, Jeng JC, et al. Whole blood- derived microRNA signatures in mice exposed to lipopolysaceharides [J ]. J Biomed Sei, 2012, 19: 69.
  • 8Potla R, Singh IS, Atamas SP, et al. Shifts in temperature within the physiologic range modify strand-specific expression of select human microRNAs [J]. RNA, 2015, 21 (7) : 1261-1273. D OI : 10.1261/rna.049122.114.
  • 9Lucherini OM, Obici L, Ferracin M, et al. First report of eireulating mieroRNAs in tumour necrosis factor receptor- associated periodie syndrome (TRAPS) [J]. PLoS One, 2013, 8 (9) : e73443.
  • 10Ayaz L, G~,rtir A, Yaroglu H~, et al. Differential expression of microRNAs in plasma of patients with laryngeal squamous cell carcinoma: potential early- detection markers for laryngeal squamous cell carcinoma [J]. J Cancer Res Clin Oncol, 2013, 139(9) : 1499-1506.

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