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对伴放线聚集杆菌和牙龈卟啉单胞菌脂多糖有反应的微小RNA调节人类巨噬细胞中调控先天免疫的基因表达。

MicroRNAs responsive to Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis LPS modulate expression of genes regulating innate immunity in human macrophages.

作者信息

Naqvi Afsar R, Fordham Jezrom B, Khan Asma, Nares Salvador

机构信息

Department of Periodontology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA Currently at Department of Periodontics, University of Illinois at Chicago, Chicago, IL, USA.

Department of Endodontics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Innate Immun. 2014 Jul;20(5):540-51. doi: 10.1177/1753425913501914. Epub 2013 Sep 23.

Abstract

MicroRNAs (miRNAs) are a class of small, noncoding RNAs that regulate post-transcriptional expression of their respective target genes and are responsive to various stimuli, including LPS. Here we examined the early (4 h) miRNA responses of THP1-differentiated macrophages challenged with LPS derived from the periodontal pathogens, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis or environmentally-modified LPS obtained from P. gingivalis grown in cigarette smoke extract. Predicted miRNA-gene target interactions for LPS-responsive miR-29b and let-7f were confirmed using dual-luciferase assays and by transfection experiments using miRNA mimics and inhibitors. Convergent and divergent miRNA profiles were observed in treated samples where differences in miRNA levels related to the type, concentration and incubation times of LPS challenge. Dual-luciferase experiments revealed miR-29b targeting of interleukin-6 receptorα (IL-6Rα) and IFN-γ inducible protein 30 and let-7f targeting of suppressor of cytokine signaling 4 and thrombospondin-1. Transfection experiments confirmed miR-29b and let-7f modulation of IL-6Rα and SOCS4 protein expression levels, respectively. Thus, we have demonstrated convergent/divergent miRNA responses to wild type LPS and its environmentally-modified LPS, and demonstrate miRNA targeting of key genes linked to inflammation and immunity. Our data indicate that these LPS-responsive miRNAs may play a key role in fine-tuning the host response to periodontal pathogens.

摘要

微小RNA(miRNA)是一类小的非编码RNA,可调节其各自靶基因的转录后表达,并对包括脂多糖(LPS)在内的各种刺激作出反应。在这里,我们研究了用源自牙周病原体伴放线聚集杆菌、牙龈卟啉单胞菌的LPS或从在香烟烟雾提取物中生长的牙龈卟啉单胞菌获得的环境修饰LPS刺激的THP1分化巨噬细胞的早期(4小时)miRNA反应。使用双荧光素酶测定法以及使用miRNA模拟物和抑制剂的转染实验,证实了LPS反应性miR-29b和let-7f的预测miRNA-基因靶标相互作用。在处理过的样品中观察到了趋同和不同的miRNA谱,其中miRNA水平的差异与LPS刺激的类型、浓度和孵育时间有关。双荧光素酶实验显示miR-29b靶向白细胞介素-6受体α(IL-6Rα)和干扰素-γ诱导蛋白30,let-7f靶向细胞因子信号转导抑制因子4和血小板反应蛋白-1。转染实验分别证实了miR-29b和let-7f对IL-6Rα和SOCS4蛋白表达水平的调节。因此,我们已经证明了对野生型LPS及其环境修饰LPS的趋同/不同miRNA反应,并证明了miRNA对与炎症和免疫相关的关键基因的靶向作用。我们的数据表明,这些LPS反应性miRNA可能在微调宿主对牙周病原体的反应中起关键作用。

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