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S100A8/A9 in Inflammation
S100A8 and S100A9 (also known as MRP8 and MRP14, respectively) are Ca(2+) binding proteins belonging to the S100 family. They often exist in the form of heterodimer, while homodimer exists very little because of the stability. S100A8/A9 is constitutively expressed in neutrophils and monocytes as a C...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004386/ https://www.ncbi.nlm.nih.gov/pubmed/29942307 http://dx.doi.org/10.3389/fimmu.2018.01298 |
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author | Wang, Siwen Song, Rui Wang, Ziyi Jing, Zhaocheng Wang, Shaoxiong Ma, Jian |
author_facet | Wang, Siwen Song, Rui Wang, Ziyi Jing, Zhaocheng Wang, Shaoxiong Ma, Jian |
author_sort | Wang, Siwen |
collection | PubMed |
description | S100A8 and S100A9 (also known as MRP8 and MRP14, respectively) are Ca(2+) binding proteins belonging to the S100 family. They often exist in the form of heterodimer, while homodimer exists very little because of the stability. S100A8/A9 is constitutively expressed in neutrophils and monocytes as a Ca(2+) sensor, participating in cytoskeleton rearrangement and arachidonic acid metabolism. During inflammation, S100A8/A9 is released actively and exerts a critical role in modulating the inflammatory response by stimulating leukocyte recruitment and inducing cytokine secretion. S100A8/A9 serves as a candidate biomarker for diagnosis and follow-up as well as a predictive indicator of therapeutic responses to inflammation-associated diseases. As blockade of S100A8/A9 activity using small-molecule inhibitors or antibodies improves pathological conditions in murine models, the heterodimer has potential as a therapeutic target. In this review, we provide a comprehensive and detailed overview of the distribution and biological functions of S100A8/A9 and highlight its application as a diagnostic and therapeutic target in inflammation-associated diseases. |
format | Online Article Text |
id | pubmed-6004386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60043862018-06-25 S100A8/A9 in Inflammation Wang, Siwen Song, Rui Wang, Ziyi Jing, Zhaocheng Wang, Shaoxiong Ma, Jian Front Immunol Immunology S100A8 and S100A9 (also known as MRP8 and MRP14, respectively) are Ca(2+) binding proteins belonging to the S100 family. They often exist in the form of heterodimer, while homodimer exists very little because of the stability. S100A8/A9 is constitutively expressed in neutrophils and monocytes as a Ca(2+) sensor, participating in cytoskeleton rearrangement and arachidonic acid metabolism. During inflammation, S100A8/A9 is released actively and exerts a critical role in modulating the inflammatory response by stimulating leukocyte recruitment and inducing cytokine secretion. S100A8/A9 serves as a candidate biomarker for diagnosis and follow-up as well as a predictive indicator of therapeutic responses to inflammation-associated diseases. As blockade of S100A8/A9 activity using small-molecule inhibitors or antibodies improves pathological conditions in murine models, the heterodimer has potential as a therapeutic target. In this review, we provide a comprehensive and detailed overview of the distribution and biological functions of S100A8/A9 and highlight its application as a diagnostic and therapeutic target in inflammation-associated diseases. Frontiers Media S.A. 2018-06-11 /pmc/articles/PMC6004386/ /pubmed/29942307 http://dx.doi.org/10.3389/fimmu.2018.01298 Text en Copyright © 2018 Wang, Song, Wang, Jing, Wang and Ma. 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 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 Wang, Siwen Song, Rui Wang, Ziyi Jing, Zhaocheng Wang, Shaoxiong Ma, Jian S100A8/A9 in Inflammation |
title | S100A8/A9 in Inflammation |
title_full | S100A8/A9 in Inflammation |
title_fullStr | S100A8/A9 in Inflammation |
title_full_unstemmed | S100A8/A9 in Inflammation |
title_short | S100A8/A9 in Inflammation |
title_sort | s100a8/a9 in inflammation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004386/ https://www.ncbi.nlm.nih.gov/pubmed/29942307 http://dx.doi.org/10.3389/fimmu.2018.01298 |
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