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Early exposure to IL-4 stabilizes IL-4 mRNA in CD4+ T cells via RNA-binding protein HuR
Journal article   Peer reviewed

Early exposure to IL-4 stabilizes IL-4 mRNA in CD4+ T cells via RNA-binding protein HuR

Timur O Yarovinsky, Noah S Butler, Martha M Monick and Gary W Hunninghake
The Journal of immunology (1950), Vol.177(7), pp.4426-4435
10/01/2006
DOI: 10.4049/jimmunol.177.7.4426
PMID: 16982877

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Abstract

The mechanisms regulating IL-4 mRNA stability in differentiated T cells are not known. We found that early exposure of CD4+ T cells to endogenous IL-4 increased IL-4 mRNA stability. This effect of IL-4 was mediated by the RNA-binding protein HuR. IL-4 mRNA interacted with HuR and the dominant binding site was shown within the coding region of IL-4 mRNA. Exposure of CD4+ T cells to IL-4 had no effects on HuR expression or subcellular localization, but triggered HuR binding to IL-4 mRNA. Thus, IL-4 plays a positive role in maintaining IL-4 mRNA stability in CD4+ T cells via a HuR-mediated mechanism.
ELAV-Like Protein 1 RNA Stability - immunology Gene Expression Protein Structure, Secondary Gene Expression Regulation - immunology Interleukin-4 - metabolism RNA, Messenger - genetics CD4-Positive T-Lymphocytes - metabolism Molecular Sequence Data Immunoblotting ELAV Proteins CD4-Positive T-Lymphocytes - immunology Microscopy, Confocal Animals Flow Cytometry Base Sequence Fluorescent Antibody Technique Antigens, Surface - metabolism RNA, Messenger - chemistry Electrophoretic Mobility Shift Assay Mice Interleukin-4 - genetics Lymphocyte Activation - physiology RNA-Binding Proteins - metabolism

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