Ahluwalia Pankaj Kumar, Pandey Rajan Kumar, Sehajpal Prabodh Kumar, Prajapati Vijay Kumar
Department of Molecular Biology and Biochemistry, Guru Nanak Dev University , Amritsar, Punjab , India.
Department of Biochemistry, School of Life Sciences, Central University of Rajasthan , Ajmer, Rajasthan , India.
Front Immunol. 2017 Feb 8;8:107. doi: 10.3389/fimmu.2017.00107. eCollection 2017.
Tuberculosis (TB) is one of the prevalent causes of death worldwide, with 95% of these deaths occurring in developing countries, like India. The causative agent, (MTb) has the tenacious ability to circumvent the host's immune system for its own advantage. Macrophages are one of the phagocytic cells that are central to immunity against MTb. These are highly plastic cells dependent on the milieu and can showcase M1/M2 polarization. M1 macrophages are bactericidal in action, but M2 macrophages are anti-inflammatory in their immune response. This computational study is an effort to elucidate the role of miRNAs that influences the survival of MTb in the macrophage. To identify the miRNAs against critical transcription factors, we selected only conserved hits from TargetScan database. Further, validation of these miRNAs was achieved using four databases . DIANA-microT, miRDB, miRanda-mirSVR, and miRNAMap. All miRNAs were identified through a conserved seed sequence against the 3'-UTR of transcription factors. This bioinformatics study found that miR-27a and miR-27b has a putative binding site at 3'-UTR of IRF4, and miR-302c against IRF5. miR-155, miR-132, and miR-455-5p are predicted microRNAs against suppressor of cytokine signaling transcription factors. Several other microRNAs, which have an affinity for critical transcription factors, are also predicted in this study. This MTb-associated modulation of microRNAs to modify the expression of the target gene(s) plays a critical role in TB pathogenesis. Other than M1/M2 plasticity, MTb has the ability to convert macrophage into foam cells that are rich in lipids and cholesterol. We have highlighted few microRNAs which overlap between M2/foam cell continuums. miR-155, miR-33, miR-27a, and miR-27b plays a dual role in deciding macrophage polarity and its conversion to foam cells. This study shows a glimpse of microRNAs which can be modulated by MTb not only to prevent its elimination but also to promote its survival.
结核病(TB)是全球主要的死亡原因之一,其中95%的死亡发生在发展中国家,如印度。病原体结核分枝杆菌(MTb)具有顽强的能力,能够为自身利益规避宿主的免疫系统。巨噬细胞是对MTb免疫至关重要的吞噬细胞之一。这些细胞具有高度可塑性,依赖于周围环境,并可表现出M1/M2极化。M1巨噬细胞具有杀菌作用,但M2巨噬细胞在免疫反应中具有抗炎作用。这项计算研究旨在阐明影响MTb在巨噬细胞中存活的miRNA的作用。为了识别针对关键转录因子的miRNA,我们仅从TargetScan数据库中选择了保守的命中结果。此外,使用四个数据库(DIANA-microT、miRDB、miRanda-mirSVR和miRNAMap)对这些miRNA进行了验证。所有miRNA均通过针对转录因子3'-UTR的保守种子序列进行识别。这项生物信息学研究发现,miR-27a和miR-27b在IRF4的3'-UTR处具有假定的结合位点,miR-302c针对IRF5。miR-155、miR-132和miR-455-5p是针对细胞因子信号传导抑制转录因子的预测miRNA。本研究还预测了其他几种对关键转录因子具有亲和力的microRNA。MTb相关的microRNA调节以改变靶基因的表达在结核病发病机制中起关键作用。除了M1/M2可塑性外,MTb还能够将巨噬细胞转化为富含脂质和胆固醇的泡沫细胞。我们强调了一些在M2/泡沫细胞连续体之间重叠的microRNA。miR-155、miR-33、miR-27a和miR-27b在决定巨噬细胞极性及其向泡沫细胞的转化中起双重作用。这项研究展示了一些可被MTb调节的microRNA,它们不仅可防止MTb被清除,还能促进其存活。