rs4719839多态性对呼吸机相关性肺炎风险、microRNA-148表达和自噬相关16样1 (ATG16L1)的影响

IF 5.3 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Journal of Cellular and Molecular Medicine Pub Date : 2020-11-01 Epub Date: 2020-09-17 DOI:10.1111/jcmm.15824
Shu-Peng Wang, Wen Li, Chen Li, Xue-Yan Duan, Jun Duan
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引用次数: 5

摘要

MiR-148是自噬16样1 (ATG16L1)的负调节因子,ATG16L1与呼吸机相关性肺炎(VAP)的发病机制有关。因此,本文研究miR-148多态性在VAP发病机制中的作用。检测VAP患者血清及外周血单个核细胞(PBMCs)中miR-148、ATG16L1、beclin -1、LC3-II、TNF-α、IL-6的表达,探讨其与VAP发病机制的关系。携带miR-148 rs4719839单核苷酸多态性(SNP)的AA/AG基因型的慢性阻塞性肺疾病患者更容易发生VAP,这是由于miR-148、TNF-α和IL-6在其血清和pbmc中表达较高,ATG16L1、beclin -1和LC3-II的表达受到抑制。将miR-148模拟物转染到基因分型为GG和AA的原代PBMCs中,可降低ATG16L1、beclin -1和LC3-II的表达。最后,携带rs4719839 SNP的AA基因型细胞对LPS刺激的作用更敏感,抑制ATG16L1、Beclin-I和LC3-II的表达,激活TNF-α和IL-6的表达。我们的工作提供了详细的证据,表明rs4719839多态性可以影响VAP的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of rs4719839 polymorphism on risk of ventilator-associated pneumonia, expression of microRNA-148 and autophagy-related 16-like 1 (ATG16L1).

Effect of rs4719839 polymorphism on risk of ventilator-associated pneumonia, expression of microRNA-148 and autophagy-related 16-like 1 (ATG16L1).

Effect of rs4719839 polymorphism on risk of ventilator-associated pneumonia, expression of microRNA-148 and autophagy-related 16-like 1 (ATG16L1).

Effect of rs4719839 polymorphism on risk of ventilator-associated pneumonia, expression of microRNA-148 and autophagy-related 16-like 1 (ATG16L1).

MiR-148 is a negative regulator of autophagy 16-like 1 (ATG16L1), a gene implicated in the pathogenesis of ventilator-associated pneumonia (VAP). Therefore, the role of miR-148 polymorphism in the pathogenesis of VAP was studied here. The expression of miR-148, ATG16L1, Beclin-I, LC3-II, TNF-α and IL-6 in serum and peripheral blood mononuclear cells (PBMCs) of VAP patients was detected to study their relationship in the pathogenesis of VAP. Chronic obstructive pulmonary disease patients carrying the AA/AG genotypes of miR-148 rs4719839 single nucleotide polymorphism (SNP) were more prone to VAP due to the higher expression of miR-148, TNF-α and IL-6 along with suppressed expression of ATG16L1, Beclin-I and LC3-II in their serum and PBMCs. Transfection of miR-148 mimics to primary PBMCs genotyped as GG and AA decreased the expression of ATG16L1, Beclin-I and LC3-II. Finally, cells carrying the AA genotype of rs4719839 SNP were more sensitive to the role of LPS stimulation in suppressing ATG16L1, Beclin-I and LC3-II expression while activating TNF-α and IL-6 expression. Our work presented detailed evidence, suggesting that the rs4719839 polymorphism can affect the risk of VAP.

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来源期刊
CiteScore
10.00
自引率
1.90%
发文量
496
审稿时长
28 weeks
期刊介绍: Bridging physiology and cellular medicine, and molecular biology and molecular therapeutics, Journal of Cellular and Molecular Medicine publishes basic research that furthers our understanding of the cellular and molecular mechanisms of disease and translational studies that convert this knowledge into therapeutic approaches.
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