HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Expression and functional characterization of retinoic acid-inducible gene-I-like receptors of mast cells in response to viral infection.

Abstract
To investigate the precise mechanisms of virus recognition by mast cells, the expression and functional characteristics of virus recognition receptors that lead to mast cell activation were investigated. Our results suggest that mast cells are partly responsible for the early in vivo production of antiviral cytokines and chemokines upon vesicular stomatitis virus (VSV) infection. Analysis of the expression of double-stranded RNA (dsRNA) recognition receptors in murine bone marrow-derived mast cells (BMMCs) revealed that BMMCs express melanoma differentiation-associated gene 5 (MDA5), protein kinase RNA-activated, retinoic acid-inducible gene-I (RIG-I) and Toll-like receptor 3. The expression levels of these receptors were found to increase upon stimulation of mast cells with VSV as well as synthetic dsRNA: polyinosinic-polycytidylic acid. Moreover, small interfering RNA analysis to identify the receptors responsible for mast cell activation by VSV revealed that both RIG-I and MDA5 were involved in cytokine production but not in the degranulation of mast cells. Our findings suggest that mast cells produce cytokines and chemokines in the early infection stage after recognizing viruses via RIG-I and MDA5, and may contribute to antiviral responses. These data provide additional novel information that improves our understanding of antiviral innate responses that involve mast cells.
AuthorsMinoru Fukuda, Hiroko Ushio, Junko Kawasaki, Francois Niyonsaba, Mizuho Takeuchi, Tadashi Baba, Keiichi Hiramatsu, Ko Okumura, Hideoki Ogawa
JournalJournal of innate immunity (J Innate Immun) Vol. 5 Issue 2 Pg. 163-73 ( 2013) ISSN: 1662-8128 [Electronic] Switzerland
PMID23171655 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 S. Karger AG, Basel.
Chemical References
  • Cytokines
  • Membrane Proteins
  • Nerve Tissue Proteins
  • RNA, Small Interfering
  • RNA, Viral
  • Receptors, Cell Surface
  • Robo3 protein, mouse
  • Toll-Like Receptor 3
  • Ifih1 protein, mouse
  • DEAD-box RNA Helicases
  • Interferon-Induced Helicase, IFIH1
Topics
  • Animals
  • Bone Marrow (immunology)
  • Cell Degranulation (genetics, immunology)
  • Cells, Cultured
  • Cytokines (metabolism)
  • DEAD-box RNA Helicases (genetics, metabolism)
  • Gene Expression Regulation
  • Immunity, Innate (genetics)
  • Interferon-Induced Helicase, IFIH1
  • Mast Cells (immunology, virology)
  • Membrane Proteins (genetics, metabolism)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nerve Tissue Proteins (genetics, metabolism)
  • RNA, Small Interfering (genetics)
  • RNA, Viral (immunology)
  • Receptors, Cell Surface
  • Toll-Like Receptor 3 (genetics, metabolism)
  • Vesicular Stomatitis (immunology)
  • Vesiculovirus (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: