4.5 Article

IFIT5 potentiates anti-viral response through enhancing innate immune signaling pathways

Journal

ACTA BIOCHIMICA ET BIOPHYSICA SINICA
Volume 45, Issue 10, Pages 867-874

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/abbs/gmt088

Keywords

IFIT5; IRF3; NF-B; innate immune response

Funding

  1. National Natural Science Foundation of China [31100946]
  2. Science and Technology Commission of Shanghai Municipality [11ZR1410000]
  3. Fundamental Research Funds for the Central Universities [78210101, 78210139]

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Humans have a distinct combination of IFIT (IFN-induced protein with tetratricopeptide repeats) family orthologs, including IFIT1 (ISG56), IFIT2 (ISG54), IFIT3 (ISG60), and IFIT5 (ISG58). The function of IFIT1/IFIT2/IFIT3 has been intensively investigated. However, little is known about the role of IFIT5 in any cellular processes. In this study, we reported that both the mRNA and protein levels of IFIT5 are up-regulated in response to RNA virus infection or polyinosiniccytidylic acid stimulation. Ectopic expression of IFIT5 could synergize IRF3- and NF-B-mediated gene expression, whereas knockdown of IFIT5 impairs the transcription of these genes. Consistently, anti-viral responses of host cells are significantly increased or decreased in the presence or absence of IFIT5. Mechanistically, IFIT5 co-localizes partly with mitochondria and interacts with RIG-I and MAVS. Our study identified that IFIT5 is an important enhancer in innate immune response.

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