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Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages
Patients with severe burn injuries are extremely susceptible to infection, and the host's antibacterial responses are frequently suppressed by alternatively activated macrophages (M2Mϕ), commonly demonstrated in these patients. An immunosuppressive subset of neutrophils (PMN-II), demonstrated i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128827/ https://www.ncbi.nlm.nih.gov/pubmed/16631375 http://dx.doi.org/10.1016/j.cyto.2006.03.001 |
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author | Yoshida, Tsuyoshi Tsuda, Yasuhiro Takeuchi, Dan Kobayashi, Makiko Pollard, Richard B. Suzuki, Fujio |
author_facet | Yoshida, Tsuyoshi Tsuda, Yasuhiro Takeuchi, Dan Kobayashi, Makiko Pollard, Richard B. Suzuki, Fujio |
author_sort | Yoshida, Tsuyoshi |
collection | PubMed |
description | Patients with severe burn injuries are extremely susceptible to infection, and the host's antibacterial responses are frequently suppressed by alternatively activated macrophages (M2Mϕ), commonly demonstrated in these patients. An immunosuppressive subset of neutrophils (PMN-II), demonstrated in the peripheral blood of thermally injured patients, has been described as an inducer of M2Mϕ. In the present studies, the inhibitory effect of glycyrrhizin (GL) on M2Mϕ generation stimulated by PMN-II was examined. M2Mϕ were generated from resident Mϕ (R-Mϕ, lower chamber) after cultivation with PMN-II (upper chamber) in a dual-chamber transwell. However, M2Mϕ were not generated from R-Mϕ when the same transwell cultures were performed in the presence of GL. M2Mϕ were not generated from R-Mϕ after cultivation with PMN-II previously treated with GL, while R-Mϕ previously treated with GL converted to M2Mϕ after they were cultured with PMN-II in transwells. Interleukin-10 and CCL2 released from PMN-II were shown to be effector molecules responsible for the generation of M2Mϕ. However, these soluble factors were not produced by PMN-II treated with GL. These results indicate that GL inhibits PMN-II-stimulated M2Mϕ generation through the inhibition of CCL2/interleukin-10 production by PMN-II. |
format | Online Article Text |
id | pubmed-7128827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71288272020-04-08 Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages Yoshida, Tsuyoshi Tsuda, Yasuhiro Takeuchi, Dan Kobayashi, Makiko Pollard, Richard B. Suzuki, Fujio Cytokine Article Patients with severe burn injuries are extremely susceptible to infection, and the host's antibacterial responses are frequently suppressed by alternatively activated macrophages (M2Mϕ), commonly demonstrated in these patients. An immunosuppressive subset of neutrophils (PMN-II), demonstrated in the peripheral blood of thermally injured patients, has been described as an inducer of M2Mϕ. In the present studies, the inhibitory effect of glycyrrhizin (GL) on M2Mϕ generation stimulated by PMN-II was examined. M2Mϕ were generated from resident Mϕ (R-Mϕ, lower chamber) after cultivation with PMN-II (upper chamber) in a dual-chamber transwell. However, M2Mϕ were not generated from R-Mϕ when the same transwell cultures were performed in the presence of GL. M2Mϕ were not generated from R-Mϕ after cultivation with PMN-II previously treated with GL, while R-Mϕ previously treated with GL converted to M2Mϕ after they were cultured with PMN-II in transwells. Interleukin-10 and CCL2 released from PMN-II were shown to be effector molecules responsible for the generation of M2Mϕ. However, these soluble factors were not produced by PMN-II treated with GL. These results indicate that GL inhibits PMN-II-stimulated M2Mϕ generation through the inhibition of CCL2/interleukin-10 production by PMN-II. Elsevier Ltd. 2006-03-21 2006-04-21 /pmc/articles/PMC7128827/ /pubmed/16631375 http://dx.doi.org/10.1016/j.cyto.2006.03.001 Text en Copyright © 2006 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Yoshida, Tsuyoshi Tsuda, Yasuhiro Takeuchi, Dan Kobayashi, Makiko Pollard, Richard B. Suzuki, Fujio Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title | Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title_full | Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title_fullStr | Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title_full_unstemmed | Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title_short | Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
title_sort | glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128827/ https://www.ncbi.nlm.nih.gov/pubmed/16631375 http://dx.doi.org/10.1016/j.cyto.2006.03.001 |
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