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不稳定型心绞痛患者CD4^+T淋巴细胞微小核糖核酸155水平与冠状动脉病变的相关性 被引量:2

Severity of coronary artery lesions with the expression of miRNA-155 in CD4^+T lymphocytes from unstable angina patients
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摘要 目的:研究外周血CD4+T淋巴细胞微小核糖核酸-155(miRNA-155)表达与血清干扰素-γ(IFN-γ)浓度和冠状动脉(冠脉)病变严重程度的相关性。方法:经冠脉造影检查后,将64例疑似不稳定型心绞痛(UAP)患者分为UAP组(经造影确诊冠心病者32例)和对照组(经造影排除冠心病者32例)。分别于冠脉造影前18~24h采集新鲜外周血,免疫磁珠法分选出CD4+T淋巴细胞,荧光定量PCR检测miRNA-155表达,酶联免疫法检测血清IFN-γ表达。并根据造影结果对冠脉病变进行Gensini评分,分析外周血CD4+T淋巴细胞miRNA-155、血清IFN-γ水平与冠脉病变Gemini评分的相关性。结果:UAP组miRNA-155、IFN-γ水平较对照组明显升高,差异有统计学意义(均P<0.05),miRNA-155和IFN-γ与冠脉病变Gensini评分呈正相关关系(r=0.534、0.713,均P<0.05)。miRNA-155和IFN-γ呈明显正相关关系(r=0.686,P<0.05)。结论:外周血CD4+T淋巴细胞miRNA-155和血清IFN-γ水平与冠脉病变程度密切相关。 Objective: To investigate the relationship between the severity of coronary artery lesions with the expression of miRNA-155 in CD4^+ T lymphocytes and the serum level of IFN-γ from unstable angina patients (UAP). Method.. According to the results of coronary angiography (CAG), 64 subjects were divided into UAP group (n=32) and normal control group (n= 32). Circulating CD4^+T cells were subsequently obtained prior to CAG,using a magnetic cell sorting system (MACS). Fluorescence-based quantitative real-time polymerase chain reaction (qRT-PCR) was then used to measure levels of miRNA-155 in the isolated CD4^+ T lymphocytes. Serum levels of IFN-γ were quantified using enzyme-linked immunosorbent assays (ELISAs). The severity of coronary lesions by CAG was evaluated by means of Gensini coronary score system. Result : Increased expression of miRNA- 155 in CD4^+T lymphocytes and serum levels of IFN-γ were observed in UAP group than in normal control group (P〈0.05). Positive correlation was found between the expression of miRNA-155 ,IFN-γ and the Gensini score of coronary artery lesion (P〈0.05). Meanwhile, positive correlation was found between the expression of miRNA- 155 and IFN-γ concentration (P〈0.05). Conclusion: miRNA-155 in CD4^+ T lymphocytes and the serum level of IFN-γ are closely related to the atherosclerostic lesions of coronary arteries.
出处 《临床心血管病杂志》 CAS CSCD 北大核心 2014年第8期702-705,共4页 Journal of Clinical Cardiology
基金 国家自然科学基金资助项目(No:81160046)
关键词 微小核糖核酸-155 干扰素-Γ CD4^+T淋巴细胞 冠状动脉病变 miRNA-15 5 interferon-γ CD4+ T lymphocytes coronary artery lesions
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  • 1李小鹰.阿司匹林在动脉硬化性心血管疾病中的临床应用:中国专家共识(2005)[J].中华心血管病杂志,2006,34(3):281-284. 被引量:193
  • 2Andersson J, Libby P, Hansson GK. Adaptive immunity and atherosclerosis [ J]. Clin Immunol, 2010, 134 ( 1 ): 33-46.
  • 3Kim VN. Small RNAs: classification, biogenesis and func- tion [J]. nol Cells, 2005, 19(1): 1-15.
  • 4Shimada K. Immune system and atherosclerotic disease: heterogeneity of leukocyte subsets participating in the path- ogenesis of atherosclerosis [ J ]. Circ J, 2009, 73 (6) : 994-1 001.
  • 5Shivdasani RA. MicroRNAs: regulators of gene expression and cell differentiation [ J ]. Blood, 2006, 108 (12) : 3 646-653.
  • 6Cobb BS, Hertweck A, Smith J, et al. A role for Dicer in immune regulation [ J ]. J Exp Med, 2006, 203 ( 11 ) : 2 519-527.
  • 7Banerjee A, Schambach F, DeJong CS, et al. Micro-RNA- 155 inhibits IFN-gamma signaling in CD4 + T cells [ J]. Eur J Immunol, 2010, 40( 1 ) : 225-231.
  • 8Rodriguez A, Vigorito E, Clare S, et al. Requirement of bic/microRNA-155 for normal immune function [ J]. Sci- ence, 2007, 316(5824): 608-611.
  • 9Rouas R, Fayyad-Kazan H, El Zein N, et al. Human nat- ural Treg microRNA signature: role of microRNA-31 and microRNA-21 in FOXP3 expression [ J]. Eur J Immunol, 2009, 39(6) : 1 608-618.
  • 10van der Fits L, van Kester MS, Qin Y, et al. MicroRNA- 21 expression in CD4+ T cells is regulated by STAT3 and is pathologically involved in Sezary syndrome [ J ]. J In- vest Dermatol, 2010, Epub ahead of print.

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