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IL-33-ST2 Axis in Liver Disease: Progression and Challenge
The new member of the IL-1 family, interleukin-33 (IL-33), participates in the progression of a variety of diseases through binding with its receptor ST2. Recently, much clinical evidence and experimental data have indicated that IL-33 is associated with various liver diseases. This review primarily...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664344/ https://www.ncbi.nlm.nih.gov/pubmed/29180837 http://dx.doi.org/10.1155/2017/5314213 |
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author | Sun, Zijian Chang, Binxia Gao, Miaomiao Zhang, Jiyuan Zou, Zhengsheng |
author_facet | Sun, Zijian Chang, Binxia Gao, Miaomiao Zhang, Jiyuan Zou, Zhengsheng |
author_sort | Sun, Zijian |
collection | PubMed |
description | The new member of the IL-1 family, interleukin-33 (IL-33), participates in the progression of a variety of diseases through binding with its receptor ST2. Recently, much clinical evidence and experimental data have indicated that IL-33 is associated with various liver diseases. This review primarily addresses the relationship between IL-33 and several hepatic diseases. IL-33 can alleviate high-fat diet- (HFD-) induced hepatic steatosis and insulin resistance, and IL-33 acts as an alarmin, which quickly triggers the immune system to respond to virus invasion and toxic damage to the liver. However, when liver injury is chronic, IL-33 promotes Th2 reactions and hepatic stellate cell (HSC) activity, facilitating progression to liver fibrosis. The complicated functions of IL-33 should be considered before its clinical application. |
format | Online Article Text |
id | pubmed-5664344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56643442017-11-27 IL-33-ST2 Axis in Liver Disease: Progression and Challenge Sun, Zijian Chang, Binxia Gao, Miaomiao Zhang, Jiyuan Zou, Zhengsheng Mediators Inflamm Review Article The new member of the IL-1 family, interleukin-33 (IL-33), participates in the progression of a variety of diseases through binding with its receptor ST2. Recently, much clinical evidence and experimental data have indicated that IL-33 is associated with various liver diseases. This review primarily addresses the relationship between IL-33 and several hepatic diseases. IL-33 can alleviate high-fat diet- (HFD-) induced hepatic steatosis and insulin resistance, and IL-33 acts as an alarmin, which quickly triggers the immune system to respond to virus invasion and toxic damage to the liver. However, when liver injury is chronic, IL-33 promotes Th2 reactions and hepatic stellate cell (HSC) activity, facilitating progression to liver fibrosis. The complicated functions of IL-33 should be considered before its clinical application. Hindawi 2017 2017-10-18 /pmc/articles/PMC5664344/ /pubmed/29180837 http://dx.doi.org/10.1155/2017/5314213 Text en Copyright © 2017 Zijian Sun et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Sun, Zijian Chang, Binxia Gao, Miaomiao Zhang, Jiyuan Zou, Zhengsheng IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title | IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title_full | IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title_fullStr | IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title_full_unstemmed | IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title_short | IL-33-ST2 Axis in Liver Disease: Progression and Challenge |
title_sort | il-33-st2 axis in liver disease: progression and challenge |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664344/ https://www.ncbi.nlm.nih.gov/pubmed/29180837 http://dx.doi.org/10.1155/2017/5314213 |
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