Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnostics in Universities of Shandong and Medical Priority Speciality of Clinical Laboratory in Shandong Province, Weifang Medical University, Weifang, Shandong 261053, P.R. China.
Department of Medical Microbiology, Weifang Medical University, Weifang, Shandong 261053, P.R. China.
Int J Mol Med. 2018 May;41(5):2885-2892. doi: 10.3892/ijmm.2018.3471. Epub 2018 Feb 7.
Cell wall deficient (CWD) forms of Mycobacterium tuberculosis (Mtb) confers a marked resistance to immune system of the host. However, there is limit data on the effect of intracellular CWD-Mtb infection on macrophages. In the study, effects of CWD-Mtb on cell viability, cytokine response and miRNA expression of macrophages were analyzed. Cell viability was reduced, levels of interleukin-1α (IL-1α), IL-1β, IL-6, IL-10 and interferon-γ (IFN-γ) were also significantly changed after infection of RAW264.7 cells with CWD-Mtb. A total of 105 miRNAs were deregulated between CWD-Mtb and wild Mtb group, and among them, miR-29b was upregulated in CWD-Mtb group. Downregulation of miR-29b resulted in significant elevation level of IFN-γ mRNA. Involved signaling pathways of potential target genes of differentially expressed miRNAs mainly focused on T cell receptor signaling pathway, MAPK signaling pathway, neurotrophin signaling pathway, and regulation of actin cytoskeleton. Taken together, the results showed that cytokine production of CWD-Mtb infected macrophages was altered and many miRNAs were involved in regulation of macrophage response to CWD-Mtb infection, which probably determined the differential outcome following different phenotype Mtb infection. These findings open up a new and interesting avenue for an improved understanding of pathogenesis of CWD-Mtb.
细胞壁缺陷 (CWD) 形式的结核分枝杆菌 (Mtb) 赋予宿主免疫系统明显的抗性。然而,关于细胞内 CWD-Mtb 感染对巨噬细胞的影响的数据有限。在这项研究中,分析了 CWD-Mtb 对巨噬细胞活力、细胞因子反应和 miRNA 表达的影响。感染 RAW264.7 细胞后,CWD-Mtb 降低了细胞活力,白细胞介素-1α (IL-1α)、IL-1β、IL-6、IL-10 和干扰素-γ (IFN-γ) 的水平也显著改变。在 CWD-Mtb 和野生 Mtb 组之间有 105 个 miRNA 失调,其中 miR-29b 在 CWD-Mtb 组中上调。miR-29b 的下调导致 IFN-γ mRNA 的水平显著升高。差异表达 miRNA 的潜在靶基因涉及的信号通路主要集中在 T 细胞受体信号通路、MAPK 信号通路、神经营养因子信号通路和肌动蛋白细胞骨架的调节。总之,这些结果表明,CWD-Mtb 感染的巨噬细胞细胞因子的产生发生改变,许多 miRNA 参与调节巨噬细胞对 CWD-Mtb 感染的反应,这可能决定了不同表型 Mtb 感染后的不同结果。这些发现为更好地理解 CWD-Mtb 的发病机制开辟了一个新的、有趣的途径。