Reach Us +1-504-608-2390
Altered MiRNA Expression In Response To Dengue Virus Infection In Human Monocytic Cells | 3382
ISSN: 2155-9899

Journal of Clinical & Cellular Immunology
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Altered miRNA expression in response to dengue virus infection in human monocytic cells

International Conference on Clinical & Cellular Immunology

Hongwei Li

ScientificTracks Abstracts: J Clin Cell Immunol

DOI: 10.4172/2155-9899.S1.002

Dengue hemorrhagic fever and dengue shock syndrome, the life-threatening forms of severe dengue virus (DENV) infection, are characterized by increased vascular permeability and plasma leakage. Human monocytes/macrophages are the primary target cells of DENV, also considered as the major sources of inflammatory cytokines that are associated with endothelial dysfunction during DENV infection. Recently miRNAs have been shown to play a regulatory role in cytokine production and inflammatory response. In this study, we analyzed expression of microRNA (miRNA) in DENV-infected monocytic cells by miRNA PCR array, and demonstrated that miRNAs that potentially target inflammation-associated genes are universally down-regulated. Using miRNA 3? UTR luciferase reporters and miRNA mimics, we have identified and validated miRNAs/gene targets that are important in dengue disease development, including miR-23b, miR-19a/b, miR-320 and miR-592 targeting TNF-alpha, miR- 19a/b targeting IL-8, miR-23b and miR-374b targeting MCP-1. Our result suggests that miRNAs function as essential modulators of inflammatory cytokine production during DENV infection and this study provides further understanding of the mechanism of dengue immunopathogenesis.
Hongwei Li received his Ph.D at National University of Singapore and completed his postdoctoral training at University of California at Riverside. His primary research interest is molecular virus-host interactions and currently focuses on the biological roles of RNAi in dengue virus-infected cells.