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Fine Particulate Air Pollution and the Expression of microRNAs and Circulating Cytokines Relevant to Inflammation, Coagulation, and Vasoconstriction

机译:细颗粒物空气污染以及与发炎,凝血和血管收缩有关的microRNA和循环细胞因子的表达

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Background: MicroRNAs (miRNAs) are a key factor in epigenetic regulation of gene expression, but miRNA responses to fine particulate matter (PM2.5) air pollution and their potential contribution to cardiovascular effects of PM2.5 are unknown. Objective: We explored the potential influence of PM2.5 on the expression of selected cytokines relevant to systemic inflammation, coagulation, and vasoconstriction, and on miRNAs that may regulate their expression. Methods: We designed a double-blind, randomized crossover study in which true and sham air purifiers were used to expose 55 healthy young adult students in Shanghai, China, to reduced or ambient levels of indoor PM2.5 during two-week periods, and we measured the expression (mRNA and protein) of 10 serum cytokines, and miRNAs that target them, after each intervention period. We used linear mixed-effect models to estimate associations of the intervention, and time-weighted personal PM2.5 exposures, with the cytokines, mRNA, and miRNAs; we also explored potential mediation by miRNAs. Results: The findings were generally consistent for associations with the intervention and for associations with an interquartile range increase in time-weighted PM2.5. Specifically, higher PM2.5 exposure was positively associated with the expression (mRNA, protein, or both) of interleukin-1 (encoded by IL1 ), IL6, tumor necrosis factor (encoded by TNF ), toll-like receptor 2 (encoded by TLR2 ), coagulation factor 3 (encoded by F3 ), and endothelin 1 (encoded by EDN1 ), and was negatively associated with miRNAs (miR-21-5p, miR-187-3p, miR-146a-5p, miR-1-3p, and miR-199a-5p) predicted to target mRNAs of IL1 , TNF , TLR2 , and EDN1 . Conclusions: Our findings require confirmation but suggest that effects of PM2.5 on cardiovascular diseases may be related to acute effects on cytokine expression, which may be partly mediated through effects of PM2.5 on miRNAs that regulate cytokine expression. https://doi.org/10.1289/EHP1447.
机译:背景:MicroRNA(miRNA)是基因表达的表观遗传调控的关键因素,但miRNA对细颗粒物(PM 2.5 )空气污染的反应及其对PM 2.5的心血管作用的潜在贡献是未知的。目的:我们探讨了PM 2.5 对与全身炎症,凝血和血管收缩相关的所选细胞因子的表达以及可能调节其表达的miRNA的潜在影响。方法:我们设计了一项双盲,随机交叉研究,其中使用真空气和假空气净化器将55名健康的上海成年青年学生暴露于室内降低的或环境水平的PM 2.5 在两个星期的周期内,我们测量了每个干预期后10种血清细胞因子以及靶向它们的miRNA的表达(mRNA和蛋白质)。我们使用线性混合效应模型来估计干预,时间加权个人PM 2.5 暴露与细胞因子,mRNA和miRNA的关联。我们还探讨了miRNA的潜在介导作用。结果:研究结果通常与干预措施的关联以及时间加权PM 2.5 的四分位数间距增加的关联一致。具体而言,较高的PM 2.5 暴露与白细胞介素-1(由IL1编码),IL6,肿瘤坏死因子(由TNF编码),toll​​-类似于受体2(由TLR2编码),凝血因子3(由F3编码)和内皮素1(由EDN1编码),并且与miRNA(miR-21-5p,miR-187-3p,miR-146a- 5p,miR-1-3p和miR-199a-5p)预计将靶向IL1,TNF,TLR2和EDN1的mRNA。结论:我们的发现尚待证实,但提示PM 2.5 对心血管疾病的影响可能与细胞因子表达的急性影响有关,这可能部分由PM 2.5 的影响介导。调节细胞因子表达的miRNA。 https://doi.org/10.1289/EHP1447。

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