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

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

机构信息

Surgical Intensive Care Unit, China-Japan Friendship Hospital, Beijing, China.

Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA.

出版信息

J Cell Mol Med. 2020 Nov;24(21):12599-12607. doi: 10.1111/jcmm.15824. Epub 2020 Sep 17.

Abstract

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.

摘要

miR-148 是自噬 16 样 1(ATG16L1)的负调控因子,该基因与呼吸机相关性肺炎(VAP)的发病机制有关。因此,本研究探讨了 miR-148 多态性在 VAP 发病机制中的作用。检测了 VAP 患者血清和外周血单个核细胞(PBMCs)中 miR-148、ATG16L1、Beclin-I、LC3-II、TNF-α和 IL-6 的表达,以研究它们在 VAP 发病机制中的关系。携带 miR-148 rs4719839 单核苷酸多态性(SNP)AA/AG 基因型的慢性阻塞性肺疾病患者更容易发生 VAP,这是由于其血清和 PBMCs 中 miR-148、TNF-α和 IL-6 的表达升高,而 ATG16L1、Beclin-I和 LC3-II 的表达受到抑制。转染 miR-148 模拟物至基因型为 GG 和 AA 的原代 PBMCs 可降低 ATG16L1、Beclin-I 和 LC3-II 的表达。最后,rs4719839 SNP 携带 AA 基因型的细胞对 LPS 刺激抑制 ATG16L1、Beclin-I 和 LC3-II 表达而激活 TNF-α和 IL-6 表达的作用更为敏感。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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7266/7686989/e31e33a154b1/JCMM-24-12599-g001.jpg

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