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The mechanism for the radioprotective effects of zymosan‐A in mice
It proved that Zymosan‐A protected the haematopoietic system from radiation‐induced damage via Toll‐Like Receptor2 in our previous study. In this study, we investigated the potential mechanism for the radioprotective effects of Zymosan‐A. The mice were treated with Zymosan‐A (50 mg/kg, dissolved in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867165/ https://www.ncbi.nlm.nih.gov/pubmed/29411511 http://dx.doi.org/10.1111/jcmm.13538 |
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author | Du, Jicong Zhang, Pei Zhao, Hainan Dong, Suhe Yang, Yanyong Cui, Jianguo Gao, Fu Cai, Jianming Liu, Cong |
author_facet | Du, Jicong Zhang, Pei Zhao, Hainan Dong, Suhe Yang, Yanyong Cui, Jianguo Gao, Fu Cai, Jianming Liu, Cong |
author_sort | Du, Jicong |
collection | PubMed |
description | It proved that Zymosan‐A protected the haematopoietic system from radiation‐induced damage via Toll‐Like Receptor2 in our previous study. In this study, we investigated the potential mechanism for the radioprotective effects of Zymosan‐A. The mice were treated with Zymosan‐A (50 mg/kg, dissolved in NS) via peritoneal injection 24 and 2 hours before ionizing radiation. Apoptosis of bone marrow cells and the levels of IL‐6, IL‐12, G‐CSF and GM‐CSF were evaluated by flow cytometry assay. DNA damage was determined by γ‐H2AX foci assay. In addition, RNA sequencing was performed to identify differentially expressed genes (DEGs). Zymosan‐A protected bone marrow cells from radiation‐induced apoptosis, up‐regulated IL‐6, IL‐12, G‐CSF and GM‐CSF in bone marrow cells. Zymosan‐A also protected cells from radiation‐induced DNA damage. Moreover, RNA sequencing analysis revealed that Zymosan‐A induced 131 DEGs involved in the regulation of immune system process and inflammatory response. The DEGs were mainly clustered in 18 KEGG pathways which were also associated with immune system processes. Zymosan‐A protected bone marrow cells from radiation‐induced apoptosis and up‐regulated IL‐6, IL‐12, G‐CSF and GM‐CSF. Moreover, Zymosan‐A might also exhibit radioprotective effects through regulating immune system process and inflammatory response. These results provided new knowledge regarding the radioprotective effect of Zymosan‐A. |
format | Online Article Text |
id | pubmed-5867165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58671652018-04-01 The mechanism for the radioprotective effects of zymosan‐A in mice Du, Jicong Zhang, Pei Zhao, Hainan Dong, Suhe Yang, Yanyong Cui, Jianguo Gao, Fu Cai, Jianming Liu, Cong J Cell Mol Med Original Articles It proved that Zymosan‐A protected the haematopoietic system from radiation‐induced damage via Toll‐Like Receptor2 in our previous study. In this study, we investigated the potential mechanism for the radioprotective effects of Zymosan‐A. The mice were treated with Zymosan‐A (50 mg/kg, dissolved in NS) via peritoneal injection 24 and 2 hours before ionizing radiation. Apoptosis of bone marrow cells and the levels of IL‐6, IL‐12, G‐CSF and GM‐CSF were evaluated by flow cytometry assay. DNA damage was determined by γ‐H2AX foci assay. In addition, RNA sequencing was performed to identify differentially expressed genes (DEGs). Zymosan‐A protected bone marrow cells from radiation‐induced apoptosis, up‐regulated IL‐6, IL‐12, G‐CSF and GM‐CSF in bone marrow cells. Zymosan‐A also protected cells from radiation‐induced DNA damage. Moreover, RNA sequencing analysis revealed that Zymosan‐A induced 131 DEGs involved in the regulation of immune system process and inflammatory response. The DEGs were mainly clustered in 18 KEGG pathways which were also associated with immune system processes. Zymosan‐A protected bone marrow cells from radiation‐induced apoptosis and up‐regulated IL‐6, IL‐12, G‐CSF and GM‐CSF. Moreover, Zymosan‐A might also exhibit radioprotective effects through regulating immune system process and inflammatory response. These results provided new knowledge regarding the radioprotective effect of Zymosan‐A. John Wiley and Sons Inc. 2018-02-07 2018-04 /pmc/articles/PMC5867165/ /pubmed/29411511 http://dx.doi.org/10.1111/jcmm.13538 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Du, Jicong Zhang, Pei Zhao, Hainan Dong, Suhe Yang, Yanyong Cui, Jianguo Gao, Fu Cai, Jianming Liu, Cong The mechanism for the radioprotective effects of zymosan‐A in mice |
title | The mechanism for the radioprotective effects of zymosan‐A in mice |
title_full | The mechanism for the radioprotective effects of zymosan‐A in mice |
title_fullStr | The mechanism for the radioprotective effects of zymosan‐A in mice |
title_full_unstemmed | The mechanism for the radioprotective effects of zymosan‐A in mice |
title_short | The mechanism for the radioprotective effects of zymosan‐A in mice |
title_sort | mechanism for the radioprotective effects of zymosan‐a in mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867165/ https://www.ncbi.nlm.nih.gov/pubmed/29411511 http://dx.doi.org/10.1111/jcmm.13538 |
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