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miR-144-3p 与感染脓肿分枝杆菌患者的病理性炎症有关。

MiR-144-3p is associated with pathological inflammation in patients infected with Mycobacteroides abscessus.

机构信息

Department of Microbiology, Chungnam National University School of Medicine, Daejeon, 35015, Korea.

Department of Medical Science, Chungnam National University School of Medicine, Daejeon, 35015, Korea.

出版信息

Exp Mol Med. 2021 Jan;53(1):136-149. doi: 10.1038/s12276-020-00552-0. Epub 2021 Jan 20.

DOI:10.1038/s12276-020-00552-0
PMID:33473145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8080579/
Abstract

Infection with rapidly growing nontuberculous mycobacteria is emerging as a global health issue; however, key host factors remain elusive. Here, we investigated the characteristic immune profiles of peripheral blood mononuclear cells (PBMCs) from patients infected with Mycobacteroides abscessus subsp. abscessus (Mabc) and M. abscessus subsp. massiliense (Mmass). Using an integrated analysis of global mRNA and microRNA expression profiles, we found that several inflammatory cytokines/chemokines [interleukin (IL)-1β, IL-6, C-X-C motif chemokine ligand 2, and C-C motif chemokine ligand 2] and miR-144-3p were significantly upregulated in PBMCs from patients compared with those from healthy controls (HCs). Notably, there was a strong correlation between the expression levels of miR-144-3p and proinflammatory cytokines/chemokines. Similarly, upregulated expression of miR-144-3p and proinflammatory cytokines/chemokines was found in macrophages and lungs from mice after infection with Mabc and Mmass. We showed that the expression of negative regulators of inflammation (SARM1 and TNIP3) was significantly downregulated in PBMCs from the patients, although they were not putative targets of miR-144-3p. Furthermore, overexpression of miR-144-3p led to a marked increase in proinflammatory cytokines/chemokines and promoted bacterial growth in macrophages. Together, our results highlight the importance of miR-144-3p linking to pathological inflammation during M. abscessus infection.

摘要

迅速生长的非结核分枝杆菌感染正在成为一个全球性的健康问题;然而,关键的宿主因素仍然难以捉摸。在这里,我们研究了感染脓肿分枝杆菌亚种脓肿(Mabc)和脓肿分枝杆菌亚种马萨诸塞(Mmass)的患者外周血单个核细胞(PBMC)的特征免疫谱。通过对全球 mRNA 和 microRNA 表达谱的综合分析,我们发现与健康对照组(HCs)相比,患者 PBMC 中几种炎症细胞因子/趋化因子[白细胞介素(IL)-1β、IL-6、C-X-C 基序趋化因子配体 2 和 C-C 基序趋化因子配体 2]和 miR-144-3p 显著上调。值得注意的是,miR-144-3p 的表达水平与促炎细胞因子/趋化因子之间存在很强的相关性。同样,在感染 Mabc 和 Mmass 后,小鼠的巨噬细胞和肺部也发现 miR-144-3p 和促炎细胞因子/趋化因子的表达上调。我们表明,患者 PBMC 中炎症负调节剂(SARM1 和 TNIP3)的表达显著下调,尽管它们不是 miR-144-3p 的推定靶标。此外,miR-144-3p 的过表达导致促炎细胞因子/趋化因子的显著增加,并促进了巨噬细胞中的细菌生长。总之,我们的研究结果强调了 miR-144-3p 在脓肿分枝杆菌感染过程中与病理性炎症相关的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/17e6e72cd21a/12276_2020_552_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/092eaf4a494c/12276_2020_552_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/cdcbf7c2f3a4/12276_2020_552_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/5d6726ee540f/12276_2020_552_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/654d9e6634bf/12276_2020_552_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/8dcdda414b35/12276_2020_552_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/17e6e72cd21a/12276_2020_552_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/092eaf4a494c/12276_2020_552_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/cdcbf7c2f3a4/12276_2020_552_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/5d6726ee540f/12276_2020_552_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/654d9e6634bf/12276_2020_552_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/8dcdda414b35/12276_2020_552_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0509/8080579/17e6e72cd21a/12276_2020_552_Fig6_HTML.jpg

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