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Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS
CD74 is expressed on the cell surface of pulmonary macrophages and contributes to macrophage migration inhibitory factor (MIF)-induced inflammatory response in acute lung injury (ALI). A circulating form of CD74 (soluble CD74, sCD74) was recently discovered in autoimmune liver disease. Using two mur...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957083/ https://www.ncbi.nlm.nih.gov/pubmed/27444250 http://dx.doi.org/10.1038/srep30067 |
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author | Wu, Guosheng Sun, Yu Wang, Kang’an Chen, Zhengli Wang, Xingtong Chang, Fei Li, Ting Feng, Ping Xia, Zhaofan |
author_facet | Wu, Guosheng Sun, Yu Wang, Kang’an Chen, Zhengli Wang, Xingtong Chang, Fei Li, Ting Feng, Ping Xia, Zhaofan |
author_sort | Wu, Guosheng |
collection | PubMed |
description | CD74 is expressed on the cell surface of pulmonary macrophages and contributes to macrophage migration inhibitory factor (MIF)-induced inflammatory response in acute lung injury (ALI). A circulating form of CD74 (soluble CD74, sCD74) was recently discovered in autoimmune liver disease. Using two murine ALI models and cells culture, we examined the presence of sCD74 in circulation and alveolar space and preliminarily assessed the biological function of sCD74. The concentrations of sCD74 were increased in serum and bronchoalveolar lavage fluids (BALF) of murine ALI models. The elevated levels of sCD74 in BALF positively correlated with lung permeability and inflammation. In addition, sCD74 is secreted by macrophages in response to MIF stimulation and itself can stimulate the production of inflammatory cytokines. Our clinical study confirmed some findings of basic research. Moreover, we also found Day 3 serum sCD74 levels were associated with worse clinical outcomes. In conclusion, higher serum sCD74 levels may reflect more severe lung injury and may be used to help physicians determine prognosis of acute respiratory distress syndrome (ARDS). |
format | Online Article Text |
id | pubmed-4957083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49570832016-07-26 Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS Wu, Guosheng Sun, Yu Wang, Kang’an Chen, Zhengli Wang, Xingtong Chang, Fei Li, Ting Feng, Ping Xia, Zhaofan Sci Rep Article CD74 is expressed on the cell surface of pulmonary macrophages and contributes to macrophage migration inhibitory factor (MIF)-induced inflammatory response in acute lung injury (ALI). A circulating form of CD74 (soluble CD74, sCD74) was recently discovered in autoimmune liver disease. Using two murine ALI models and cells culture, we examined the presence of sCD74 in circulation and alveolar space and preliminarily assessed the biological function of sCD74. The concentrations of sCD74 were increased in serum and bronchoalveolar lavage fluids (BALF) of murine ALI models. The elevated levels of sCD74 in BALF positively correlated with lung permeability and inflammation. In addition, sCD74 is secreted by macrophages in response to MIF stimulation and itself can stimulate the production of inflammatory cytokines. Our clinical study confirmed some findings of basic research. Moreover, we also found Day 3 serum sCD74 levels were associated with worse clinical outcomes. In conclusion, higher serum sCD74 levels may reflect more severe lung injury and may be used to help physicians determine prognosis of acute respiratory distress syndrome (ARDS). Nature Publishing Group 2016-07-22 /pmc/articles/PMC4957083/ /pubmed/27444250 http://dx.doi.org/10.1038/srep30067 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wu, Guosheng Sun, Yu Wang, Kang’an Chen, Zhengli Wang, Xingtong Chang, Fei Li, Ting Feng, Ping Xia, Zhaofan Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title | Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title_full | Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title_fullStr | Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title_full_unstemmed | Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title_short | Relationship between elevated soluble CD74 and severity of experimental and clinical ALI/ARDS |
title_sort | relationship between elevated soluble cd74 and severity of experimental and clinical ali/ards |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957083/ https://www.ncbi.nlm.nih.gov/pubmed/27444250 http://dx.doi.org/10.1038/srep30067 |
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