Expression profile and function of miRNAs in macrophages infected with Mycobacterium
10.16438/j.0513-4870.2024-0278
- VernacularTitle:分枝杆菌感染巨噬细胞中miRNA表达谱及其功能
- Author:
Ping-ping JIA
1
;
Yi ZHANG
2
;
Shi-ze PENG
2
;
Qian-qian ZHAO
1
;
Xiao-xiao WU
1
;
Fang-qi SHEN
1
;
Kai SUN
1
;
Shan CEN
2
Author Information
1. Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China
2. Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
- Publication Type:Research Article
- Keywords:
italic>Mycobacterium tuberculosis;
infecting host;
miRNA;
intracellular survival;
regulation
- From:
Acta Pharmaceutica Sinica
2024;59(6):1674-1679
- CountryChina
- Language:Chinese
-
Abstract:
The interaction between Mycobacterium tuberculosis and host, as well as the regulation of some signaling pathways in the host, were involved in pathogen latency in macrophages. microRNAs (miRNAs) regulate the gene expression and biological functions, indicating that miRNAs played a regulatory role in bacterial infections. However, whether the host's miRNAs were also involved in the process of Mycobacterium tuberculosis infection had not been thoroughly studied. This study infected macrophages with pathogenic Mycobacterium tuberculosis strain H37Rv and low virulence strain H37Ra to explore the functional miRNAs. By identifying the expression profile of miRNAs in host cells after infection, the expression of 17 miRNAs significantly changed (P < 0.05) in the human macrophage THP-1 infected with highly pathogenic H37Rv strain (Rv), H37Rv inactivated strain (Rv-), and non-pathogenic H37Ra (Ra) strains respectively, indicating that host miRNAs may be involved in the interaction of Mycobacterium tuberculosis and host. Meanwhile, 10 types of miRNAs showed significant differences in cells infected with pathogenic and non-pathogenic Mycobacterium tuberculosis, suggesting that host miRNAs may play an important role in the pathogenicity and intracellular survival of Mycobacterium tuberculosis. Further study had found that miR-449a, miR-502-5p, and miR-708 were downregulated in cells infected with Mycobacterium marinum. Overexpression of these three miRNAs displayed the significant inhibitory effect on the growth of Mycobacterium marinum, indicating that miRNAs played a pivotal role in the interaction between the host and Mycobacterium marinum. This study provided the new insights into the pathogenesis of Mycobacterium tuberculosis and the treatment of tuberculosis.
