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Regulation of innate immune signaling by IRAK proteins
The Toll-like receptors (TLRs) and interleukin-1 receptors (IL-1R) families are of paramount importance in coordinating the early immune response to pathogens. Signaling via most TLRs and IL-1Rs is mediated by the protein myeloid differentiation primary-response protein 88 (MyD88). This signaling ad...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972678/ https://www.ncbi.nlm.nih.gov/pubmed/36865541 http://dx.doi.org/10.3389/fimmu.2023.1133354 |
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author | Pereira, Milton Gazzinelli, Ricardo T. |
author_facet | Pereira, Milton Gazzinelli, Ricardo T. |
author_sort | Pereira, Milton |
collection | PubMed |
description | The Toll-like receptors (TLRs) and interleukin-1 receptors (IL-1R) families are of paramount importance in coordinating the early immune response to pathogens. Signaling via most TLRs and IL-1Rs is mediated by the protein myeloid differentiation primary-response protein 88 (MyD88). This signaling adaptor forms the scaffold of the myddosome, a molecular platform that employs IL-1R-associated kinase (IRAK) proteins as main players for transducing signals. These kinases are essential in controlling gene transcription by regulating myddosome assembly, stability, activity and disassembly. Additionally, IRAKs play key roles in other biologically relevant responses such as inflammasome formation and immunometabolism. Here, we summarize some of the key aspects of IRAK biology in innate immunity. |
format | Online Article Text |
id | pubmed-9972678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99726782023-03-01 Regulation of innate immune signaling by IRAK proteins Pereira, Milton Gazzinelli, Ricardo T. Front Immunol Immunology The Toll-like receptors (TLRs) and interleukin-1 receptors (IL-1R) families are of paramount importance in coordinating the early immune response to pathogens. Signaling via most TLRs and IL-1Rs is mediated by the protein myeloid differentiation primary-response protein 88 (MyD88). This signaling adaptor forms the scaffold of the myddosome, a molecular platform that employs IL-1R-associated kinase (IRAK) proteins as main players for transducing signals. These kinases are essential in controlling gene transcription by regulating myddosome assembly, stability, activity and disassembly. Additionally, IRAKs play key roles in other biologically relevant responses such as inflammasome formation and immunometabolism. Here, we summarize some of the key aspects of IRAK biology in innate immunity. Frontiers Media S.A. 2023-02-14 /pmc/articles/PMC9972678/ /pubmed/36865541 http://dx.doi.org/10.3389/fimmu.2023.1133354 Text en Copyright © 2023 Pereira and Gazzinelli https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Pereira, Milton Gazzinelli, Ricardo T. Regulation of innate immune signaling by IRAK proteins |
title | Regulation of innate immune signaling by IRAK proteins |
title_full | Regulation of innate immune signaling by IRAK proteins |
title_fullStr | Regulation of innate immune signaling by IRAK proteins |
title_full_unstemmed | Regulation of innate immune signaling by IRAK proteins |
title_short | Regulation of innate immune signaling by IRAK proteins |
title_sort | regulation of innate immune signaling by irak proteins |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972678/ https://www.ncbi.nlm.nih.gov/pubmed/36865541 http://dx.doi.org/10.3389/fimmu.2023.1133354 |
work_keys_str_mv | AT pereiramilton regulationofinnateimmunesignalingbyirakproteins AT gazzinelliricardot regulationofinnateimmunesignalingbyirakproteins |