High serum miR-183 level is associated with the bioactivity of macrophage derived from tuberculosis patients
- PMID: 25755759
- PMCID: PMC4348860
High serum miR-183 level is associated with the bioactivity of macrophage derived from tuberculosis patients
Abstract
As a major health threat, tuberculosis (TB) is resistant against the current therapeutic strategies. Increasing evidence indicates that miRNAs are implicated in various disorders by affecting specific target genes. Recently, the association of miRNAs with TB has also been established by several studies, and their potentials in the prognosis and treatment of TB have also been verified. miR-183 is shown to promote the activation of macrophage through NF-κB pathway. However, it is still unclear if serum miR-183 can be used to assess the activity of TB-associated macrophage. This study was aimed to address this issue. We employed qPCR assay to detect the expression level of miR-183 in blood from TB patients and healthy individuals. miR-183 abundance was found to be increased in serum samples from TB patients, compared with healthy controls. Further analysis revealed that miR-183 level is positively associated with the activity of macrophages from TB patients, evidenced by their increased phagocytosis rates and enzyme activity in high serum miR-183 group. In conclusions, high level of serum miR-183 is associated with the activity of macrophage originating from TB patients.
Keywords: Tuberculosis; macrophage; miR-183.
Figures



Similar articles
-
Characterization of a novel panel of plasma microRNAs that discriminates between Mycobacterium tuberculosis infection and healthy individuals.PLoS One. 2017 Sep 14;12(9):e0184113. doi: 10.1371/journal.pone.0184113. eCollection 2017. PLoS One. 2017. PMID: 28910318 Free PMC article. Clinical Trial.
-
Levels of microRNA miR-16 and miR-155 are altered in serum of patients with tuberculosis and associate with responses to therapy.Tuberculosis (Edinb). 2017 Jan;102:24-30. doi: 10.1016/j.tube.2016.10.007. Epub 2016 Nov 1. Tuberculosis (Edinb). 2017. PMID: 28061948
-
Differential microRNAs expression in serum of patients with lung cancer, pulmonary tuberculosis, and pneumonia.Cell Biochem Biophys. 2013;67(3):875-84. doi: 10.1007/s12013-013-9575-y. Cell Biochem Biophys. 2013. PMID: 23559272
-
MicroRNA-223 Is Upregulated in Active Tuberculosis Patients and Inhibits Apoptosis of Macrophages by Targeting FOXO3.Genet Test Mol Biomarkers. 2015 Dec;19(12):650-6. doi: 10.1089/gtmb.2015.0090. Epub 2015 Oct 27. Genet Test Mol Biomarkers. 2015. PMID: 26505221
-
Macrophage immunoregulatory pathways in tuberculosis.Semin Immunol. 2014 Dec;26(6):471-85. doi: 10.1016/j.smim.2014.09.010. Epub 2014 Oct 30. Semin Immunol. 2014. PMID: 25453226 Free PMC article. Review.
Cited by
-
Diagnostic Value of Serum miR-182, miR-183, miR-210, and miR-126 Levels in Patients with Early-Stage Non-Small Cell Lung Cancer.PLoS One. 2016 Apr 19;11(4):e0153046. doi: 10.1371/journal.pone.0153046. eCollection 2016. PLoS One. 2016. PMID: 27093275 Free PMC article.
-
MicroRNAs as Regulators of Phagocytosis.Cells. 2022 Apr 19;11(9):1380. doi: 10.3390/cells11091380. Cells. 2022. PMID: 35563685 Free PMC article. Review.
-
Epigenetic Biomarkers of Renal Cell Carcinoma for Liquid Biopsy Tests.Int J Mol Sci. 2021 Aug 17;22(16):8846. doi: 10.3390/ijms22168846. Int J Mol Sci. 2021. PMID: 34445557 Free PMC article. Review.
-
Non-Coding RNAs in Tuberculosis Epidemiology: Platforms and Approaches for Investigating the Genome's Dark Matter.Int J Mol Sci. 2022 Apr 17;23(8):4430. doi: 10.3390/ijms23084430. Int J Mol Sci. 2022. PMID: 35457250 Free PMC article. Review.
-
Profiling the mRNA and miRNA in Peripheral Blood Mononuclear Cells in Subjects with Active Tuberculosis.Infect Drug Resist. 2020 Nov 23;13:4223-4234. doi: 10.2147/IDR.S278705. eCollection 2020. Infect Drug Resist. 2020. PMID: 33262617 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials