首页> 外文期刊>Frontiers in Microbiology >Leishmania donovani Activates Hypoxia Inducible Factor-1α and miR-210 for Survival in Macrophages by Downregulation of NF-κB Mediated Pro-inflammatory Immune Response
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Leishmania donovani Activates Hypoxia Inducible Factor-1α and miR-210 for Survival in Macrophages by Downregulation of NF-κB Mediated Pro-inflammatory Immune Response

机译:多发性利什曼原虫通过下调NF-κB介导的促炎性免疫反应激活低氧诱导因子-1α和miR-210在巨噬细胞中存活。

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Micro RNAs (miRNAs) have emerged as a critical regulator of several biological processes in both animals and plants. They have also been associated with regulation of immune responses in many human diseases during recent years. Visceral leishmaniasis (VL) is the most severe form of leishmaniasis, which is characterized by impairment of both innate and adaptive immune responses. In the present study, we observed that Leishmania establishes hypoxic environment in host macrophages that induces the expression of hypoxia inducible factor-1α (HIF-1α) and miRNA-210. Further, the expression of miRNA-210 was found to be dependent on activation of HIF-1α expression. The HIF-1α silencing by siRNA resulted in significantly ( p < 0.001) decreased expression of miR-210 in parasites infected macrophages. We also observed that in siHIF-1α or antagomir-210 treated L. donovani infected macrophages, the parasitic load and percentage infectivity were significantly ( p < 0.001) decreased. Furthermore, we found that inhibition of miR-210 leads to activation of NF-κB subunit p50, and it forms heterodimer with p65 and translocates into the nucleus from the cytoplasm. This significantly ( p < 0.05) induced the transcription of pro-inflammatory cytokines genes such as TNF-α and IL-12 in miRNA-210 inhibited macrophages compared to uninhibited macrophages whereas the level of IL-10, an anti-inflammatory cytokine, was found to be significantly decreased ( p < 0.001). These findings suggested that L. donovani infection induces hypoxic environment inside the macrophages that activates HIF-1α. Further, HIF-1α upregulates miR-210, which eventually establishes a suitable environment for the survival of parasite inside the host macrophages by downregulating NF-κB mediated pro-inflammatory immune responses.
机译:微小RNA(miRNA)已成为动植物中几种生物过程的关键调节剂。近年来,它们还与许多人类疾病的免疫应答调节有关。内脏利什曼病(VL)是利什曼病的最严重形式,其特征是先天和适应性免疫反应均受损。在本研究中,我们观察到利什曼原虫在宿主巨噬细胞中建立了低氧环境,该环境诱导了缺氧诱导因子-1α(HIF-1α)和miRNA-210的表达。此外,发现miRNA-210的表达依赖于HIF-1α表达的激活。 siRNA使HIF-1α沉默导致寄生虫感染的巨噬细胞中miR-210的表达显着降低(p <0.001)。我们还观察到,在siHIF-1α或antagomir-210处理的多诺尼乳杆菌感染的巨噬细胞中,寄生虫负荷和感染率显着降低(p <0.001)。此外,我们发现抑制miR-210会导致NF-κB亚基p50的激活,并且它与p65形成异源二聚体并从细胞质转移到细胞核中。与未抑制的巨噬细胞相比,这显着(p <0.05)诱导了miRNA-210抑制的巨噬细胞中促炎性细胞因子基因(如TNF-α和IL-12)的转录,而抗炎性细胞因子IL-10的水平为被发现显着下降(P <0.001)。这些发现表明,多诺氏乳杆菌感染在激活HIF-1α的巨噬细胞内诱导了低氧环境。此外,HIF-1α上调miR-210,从而通过下调NF-κB介导的促炎性免疫应答,最终为宿主巨噬细胞内的寄生虫的存活建立合适的环境。

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