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Differential Expression of Human MicroRNAs During Dengue Virus Infection in THP-1 Monocytes.

Authors :
Rossi ÁD
Higa LM
Herlinger AL
Ribeiro-Alves M
de Menezes MT
Giannini ALM
Cardoso CC
Da Poian AT
Tanuri A
Aguiar RS
Source :
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2021 Sep 08; Vol. 11, pp. 714088. Date of Electronic Publication: 2021 Sep 08 (Print Publication: 2021).
Publication Year :
2021

Abstract

Dengue virus (DENV) is the most widespread arbovirus, responsible for a wide range of clinical manifestations, varying from self-limited illness to severe hemorrhagic fever. Dengue severity is associated with host intense proinflammatory response and monocytes have been considered one of the key cell types involved in the early steps of DENV infection and immunopathogenesis. To better understand cellular mechanisms involved in monocyte infection by DENV, we analyzed the expression levels of 754 human microRNAs in DENV-infected THP-1 cells, a human monocytic cell line. Eleven human microRNAs showed differential expression after DENV infection and gene ontology and enrichment analysis revealed biological processes potentially affected by these molecules. Five downregulated microRNAs were significantly linked to cellular response to stress, four to cell death/apoptosis, two to innate immune responses and one upregulated to vesicle mediated, TGF-β signaling, phosphatidylinositol mediated signaling, lipid metabolism process and blood coagulation.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Rossi, Higa, Herlinger, Ribeiro-Alves, de Menezes, Giannini, Cardoso, Da Poian, Tanuri and Aguiar.)

Details

Language :
English
ISSN :
2235-2988
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in cellular and infection microbiology
Publication Type :
Academic Journal
Accession number :
34568093
Full Text :
https://doi.org/10.3389/fcimb.2021.714088