Journal
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
Volume 11, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.714088
Keywords
microRNA; monocyte; dengue; gene expression; virus-host
Categories
Funding
- Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro - FAPERJ [201.316/2016, 202.945/2017]
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq [309028/2017-5, 312688/2017-2, 439119/2018-9]
- La Caixa Bank Foundation [LCF/PR/HR17/52150011]
- FAPERJ [E-26/010.001278/2016, 202.922/2018]
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An analysis of the expression levels of 754 human microRNAs in DENV-infected THP-1 cells revealed differential expression of 11 human microRNAs, with gene ontology and enrichment analysis highlighting potential biological processes affected by these molecules.
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-beta signaling, phosphatidylinositol mediated signaling, lipid metabolism process and blood coagulation.
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