下调hsa_circ_0045474通过miR-582-5p/TNKS2轴诱导结核中巨噬细胞自噬。

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Innate Immunity Pub Date : 2022-01-01 Epub Date: 2021-12-03 DOI:10.1177/17534259211064285
Min Wu, Zhibin Liu, Shaojun Zhang
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引用次数: 7

摘要

巨噬细胞自噬在控制和消灭入侵的结核分枝杆菌中起着重要作用。然而,circRNA在结核病巨噬细胞自噬中的作用和机制尚不清楚。因此,本研究旨在探讨circRNA在结核病中巨噬细胞自噬中的作用。采用实时定量聚合酶链反应检测hsa_circ_0045474、miR-582-5p、TNKS2的表达。LC3B免疫荧光和透射电镜检测细胞自噬。采用双荧光素酶报告试验检测miR-582-5p与hsa_circ_0045474或TNKS2的关系。Western blot检测LC3-І和LC3-ІІ的表达。结果显示hsa_circ_0045474在结核患者单核细胞中下调,诱导巨噬细胞自噬。hsa_circ_0045474海绵miR-582-5p并负向调节miR-582-5p的表达。受hsa_circ_0045474影响的miR-582-5p过表达诱导巨噬细胞自噬。TNKS2作为miR-582-5p的靶标,miR-582-5p调控的巨噬细胞中TNKS2的下调诱导自噬。总之,我们的研究结果表明,hsa_circ_0045474下调通过miR-582-5p/ TNKS2轴诱导结核中的巨噬细胞自噬,这意味着治疗结核分枝杆菌免疫逃逸引起的活动性肺结核的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Down-regulation of hsa_circ_0045474 induces macrophage autophagy in tuberculosis via miR-582-5p/TNKS2 axis.

Macrophage autophagy plays a major role in the control and elimination of invading Mycobacterium tuberculosis. However, the function and mechanism of circRNA on macrophage autophagy in tuberculosis remain unclear. Therefore, this study aimed to explore the role of circRNA underlying macrophage autophagy in tuberculosis. Quantitative real-time polymerase chain reaction was used to detect the expression of hsa_circ_0045474, miR-582-5p and TNKS2. Autophagy was detected by LC3B immunofluorescence and transmission electron microscopy. Dual-luciferase reporter assays were used to detect the relationship of miR-582-5p and hsa_circ_0045474 or TNKS2. Western blot was used to detect the expression of LC3-І and LC3-ІІ. The results showed that hsa_circ_0045474 was down-regulated in monocytes from patients with tuberculosis and induced autophagy in macrophages. hsa_circ_0045474 sponged miR-582-5p and negatively regulated miR-582-5p expression. Overexpression of miR-582-5p affected by hsa_circ_0045474 induced autophagy in macrophages. TNKS2 served as a target of miR-582-5p and down-regulation of TNKS2 induced autophagy in macrophages regulated by miR-582-5p. In conclusion, our results demonstrated that hsa_circ_0045474 down-regulation induced macrophage autophagy in tuberculosis via miR-582-5p/ TNKS2 axis, implying a novel strategy to treat the occurrence of active pulmonary tuberculosis caused by immune escape of M. tuberculosis.

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来源期刊
Innate Immunity
Innate Immunity 生物-免疫学
CiteScore
7.20
自引率
0.00%
发文量
20
审稿时长
6-12 weeks
期刊介绍: Innate Immunity is a highly ranked, peer-reviewed scholarly journal and is the official journal of the International Endotoxin & Innate Immunity Society (IEIIS). The journal welcomes manuscripts from researchers actively working on all aspects of innate immunity including biologically active bacterial, viral, fungal, parasitic, and plant components, as well as relevant cells, their receptors, signaling pathways, and induced mediators. The aim of the Journal is to provide a single, interdisciplinary forum for the dissemination of new information on innate immunity in humans, animals, and plants to researchers. The Journal creates a vehicle for the publication of articles encompassing all areas of research, basic, applied, and clinical. The subject areas of interest include, but are not limited to, research in biochemistry, biophysics, cell biology, chemistry, clinical medicine, immunology, infectious disease, microbiology, molecular biology, and pharmacology.
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