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鉴定和分析巨噬细胞中新型感染相关转录本。

Identification and characterization of novel infection associated transcripts in macrophages.

机构信息

Department of Cardio- Respiratory Disease Biology, CSIR Institute of Genomics and Integrative Biology, Mathura Road, New Delhi-110025, India.

Department of Biological Sciences, Academy of Scientific and Innovative Research, CSIR- HRDC campus, Sector 19, Kamla Nehru Nagar, Ghaziabad- 201002, India.

出版信息

RNA Biol. 2021 Nov 12;18(sup2):604-611. doi: 10.1080/15476286.2021.1989217. Epub 2021 Nov 8.

DOI:10.1080/15476286.2021.1989217
PMID:34747322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8782167/
Abstract

By analysis of lncRNA expression profiles of macrophages in response to (Mtb) infection, we identified novel highly expressed transcripts, unique in encompassing a protein coding transcript- Cytidine Monophosphate Kinase 2 (CMPK2) and a previously identified lncRNA- Negative Regulator of Interferon Response (NRIR). While these transcripts (TILT1, 2,3 - LR4 and nfection induced ong ranscript) are induced by virulent Mtb as well as lipopolysaccharide (LPS) early, lack of/delayed expression in non-viable Mtb/BCG infected cells, respectively, suggest an important role in macrophage responses. The elevated expression by 3 hr in response to fast growing bacteria further emphasizes the importance of these RNAs in the macrophage infection response. Overall, we provide evidence for the presence of multiple transcripts that form a part of the early infection response programme of macrophages. IFN: Interferon; NRIR: negative regulator of interferon response; CMPK2: cytidine/ uridine monophosphate kinase; LPS: lipopolysaccharide; LAM: Lipoarabinomannan; PIMs: Phosphatidylinositol Mannosides; TILT1, 2,3: LR4 and nfection induced ong ranscript; TLR4: Toll-like receptor 4; Mtb: ; BCG: BCG; MDMs: human monocyte derived macrophages.

摘要

通过分析巨噬细胞对(Mtb)感染的长链非编码 RNA 表达谱,我们鉴定出了新型高表达的转录本,这些转录本独特之处在于包含一个编码蛋白的转录本——胞苷一磷酸激酶 2(CMPK2)和一个先前鉴定的长链非编码 RNA——干扰素反应负调控因子(NRIR)。虽然这些转录本(TILT1、2、3-LR4 和感染诱导的长转录本)被毒力 Mtb 以及脂多糖(LPS)早期诱导,但在非存活 Mtb/BCG 感染细胞中分别缺乏/延迟表达,提示它们在巨噬细胞反应中具有重要作用。这些 RNA 在快速生长的细菌刺激下 3 小时即可显著上调,进一步强调了它们在巨噬细胞感染反应中的重要性。综上所述,我们提供了证据证明存在多个转录本,这些转录本构成了巨噬细胞早期感染反应程序的一部分。IFN:干扰素;NRIR:干扰素反应负调控因子;CMPK2:胞苷/尿苷一磷酸激酶;LPS:脂多糖;LAM:阿拉伯甘露聚糖脂;PIMs:磷酸化酰基肌醇甘露糖苷;TILT1、2、3-LR4 和感染诱导的长转录本;TLR4:Toll 样受体 4;Mtb:结核分枝杆菌;BCG:卡介苗;MDMs:人单核细胞衍生的巨噬细胞。

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