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首页|期刊导航|安徽医科大学学报|lncRNA NEAT1在结核分枝杆菌感染RAW264.7巨噬细胞中的表达及作用的初步探讨

lncRNA NEAT1在结核分枝杆菌感染RAW264.7巨噬细胞中的表达及作用的初步探讨

黄舒颖 张诚 黄自坤 罗清 卿城

安徽医科大学学报2019,Vol.54Issue(2):212-216,5.
安徽医科大学学报2019,Vol.54Issue(2):212-216,5.DOI:10.19405/j.cnki.issn1000-1492.2019.02.010

lncRNA NEAT1在结核分枝杆菌感染RAW264.7巨噬细胞中的表达及作用的初步探讨

The expression and function of lncRNA NEAT1 in RAW264. 7 macrophages infected with Mycobacterium tuberculosis

黄舒颖 1张诚 2黄自坤 3罗清 4卿城4

作者信息

  • 1. 南昌大学第一附属医院妇产科,南昌 330006
  • 2. 江西卫生职业学院护理系,南昌 330052
  • 3. 南昌大学第一附属医院超声科,南昌 330006
  • 4. 南昌大学第一附属医院检验科,南昌 330006
  • 折叠

摘要

Abstract

Objective To detect the expression changes of lncRNA NEAT1 in RAW264. 7 macrophages after infected with tuberculosis. By lowering the expression of NEAT1 in cells,the role of its in anti-tuberculosis immune response in macrophages was preliminarily discussed. Methods RAW264. 7 macrophages were infected with H37Rv,cells and culture supernatant were collected in the 12 h,24 h,48 h time points. Respectively,RT-qPCR was used to detect intracellular NEAT1 expression,and ELISA assay was used to detect IL-6 expression in culture supernatant. By using RNAi,NEAT1 was silenced in macrophages,and after H37Rv infection,the secretion of was detected,and the change of bactericidal capacity agasint MTB was assessed. Results Test results showed that the expression of NEAT1 and secretion of IL-6 were both significantly increased (P < 0. 01). By silencing NEAT1 in macrophages,there was a significant decrease in secretion of IL-6 (P < 0. 01),and the ability of MTB removal was significantly decreased (P < 0. 01). Conclusion H37Rv infection RAW264. 7 macrophages can promote NEAT1 expression,silencing NEAT1 can reduce the clearance of intracellular MTB by macrophages.

关键词

结核分枝杆菌/lncRNA NEAT1/RAW264. 7 巨噬细胞

Key words

Mycobacterium tuberculosis/lncRNA NEAT1/RAW264. 7 macrophages

分类

医药卫生

引用本文复制引用

黄舒颖,张诚,黄自坤,罗清,卿城..lncRNA NEAT1在结核分枝杆菌感染RAW264.7巨噬细胞中的表达及作用的初步探讨[J].安徽医科大学学报,2019,54(2):212-216,5.

基金项目

江西省自然科学基金(编号: 20171BAB205028、20161BAB215224) (编号: 20171BAB205028、20161BAB215224)

江西省教育厅科学技术研究项目(编号:GJJ160120) (编号:GJJ160120)

江西省卫生计生委科技计划项目(编号:20185084) (编号:20185084)

安徽医科大学学报

OA北大核心CSTPCD

1000-1492

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