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Characterization of a long isoform of IL-1R8 (TIR8/SIGIRR)

Maria Giovanna Vilia, Marta Tocchetti, Eleonora Fonte, Ilenia Sana, Marta Muzio

Cell signaling unit, division of experimental oncology, IRCCS San Raffaele hospital, Milano, Italy

* Corresponding Author: Marta Muzio, email

European Cytokine Network 2017, 28(2), 63-69. https://doi.org/10.1684/ecn.2017.0395

Abstract

IL-1R8, also known as SIGIRR or TIR8, is a trans-membrane protein belonging to the IL-1 receptor family. The human gene includes ten exons, and alternative splicing can result in different isoforms. We, herein, characterized a longer isoform of IL-1R8 containing an in-frame additional sequence between the TIR domain and the C-terminal portion of the protein. IL-1R8 Long (IL-1R8L1) mRNA was specifically expressed and regulated in distinct cell lines, in a manner similar to the classic isoform. Overexpression of IL-1R8L1 resulted in the production of a corresponding protein that showed a pattern of cell localization similar to the classic isoform. An antibody directed against an IL-1R8L1 specific peptide, detected this novel isoform in different cell lines and tissues where this protein may complement the anti-inflammatory functions of classic IL-1R8.

Keywords

interleukin-1 receptor, Toll-like receptor, IL-1R8, TIR8, SIGIRR, splicing

Cite This Article

APA Style
Vilia, M.G., Tocchetti, M., Fonte, E., Sana, I., Muzio, M. (2017). Characterization of a long isoform of IL-1R8 (TIR8/SIGIRR). European Cytokine Network, 28(2), 63–69. https://doi.org/10.1684/ecn.2017.0395
Vancouver Style
Vilia MG, Tocchetti M, Fonte E, Sana I, Muzio M. Characterization of a long isoform of IL-1R8 (TIR8/SIGIRR). Eur Cytokine Network. 2017;28(2):63–69. https://doi.org/10.1684/ecn.2017.0395
IEEE Style
M.G. Vilia, M. Tocchetti, E. Fonte, I. Sana, and M. Muzio, “Characterization of a long isoform of IL-1R8 (TIR8/SIGIRR),” Eur. Cytokine Network, vol. 28, no. 2, pp. 63–69, 2017. https://doi.org/10.1684/ecn.2017.0395



cc Copyright © 2017 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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