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Faecal microbiota transplantation protects against radiation‐induced toxicity
Severe radiation exposure may cause acute radiation syndrome, a possibly fatal condition requiring effective therapy. Gut microbiota can be manipulated to fight against many diseases. We explored whether intestinal microbe transplantation could alleviate radiation‐induced toxicity. High‐throughput s...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376756/ https://www.ncbi.nlm.nih.gov/pubmed/28242755 http://dx.doi.org/10.15252/emmm.201606932 |
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author | Cui, Ming Xiao, Huiwen Li, Yuan Zhou, Lixin Zhao, Shuyi Luo, Dan Zheng, Qisheng Dong, Jiali Zhao, Yu Zhang, Xin Zhang, Junling Lu, Lu Wang, Haichao Fan, Saijun |
author_facet | Cui, Ming Xiao, Huiwen Li, Yuan Zhou, Lixin Zhao, Shuyi Luo, Dan Zheng, Qisheng Dong, Jiali Zhao, Yu Zhang, Xin Zhang, Junling Lu, Lu Wang, Haichao Fan, Saijun |
author_sort | Cui, Ming |
collection | PubMed |
description | Severe radiation exposure may cause acute radiation syndrome, a possibly fatal condition requiring effective therapy. Gut microbiota can be manipulated to fight against many diseases. We explored whether intestinal microbe transplantation could alleviate radiation‐induced toxicity. High‐throughput sequencing showed that gastrointestinal bacterial community composition differed between male and female mice and was associated with susceptibility to radiation toxicity. Faecal microbiota transplantation (FMT) increased the survival rate of irradiated animals, elevated peripheral white blood cell counts and improved gastrointestinal tract function and intestinal epithelial integrity in irradiated male and female mice. FMT preserved the intestinal bacterial composition and retained mRNA and long non‐coding RNA expression profiles of host small intestines in a sex‐specific fashion. Despite promoting angiogenesis, sex‐matched FMT did not accelerate the proliferation of cancer cells in vivo. FMT might serve as a therapeutic to mitigate radiation‐induced toxicity and improve the prognosis of tumour patients after radiotherapy. |
format | Online Article Text |
id | pubmed-5376756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53767562017-04-05 Faecal microbiota transplantation protects against radiation‐induced toxicity Cui, Ming Xiao, Huiwen Li, Yuan Zhou, Lixin Zhao, Shuyi Luo, Dan Zheng, Qisheng Dong, Jiali Zhao, Yu Zhang, Xin Zhang, Junling Lu, Lu Wang, Haichao Fan, Saijun EMBO Mol Med Research Articles Severe radiation exposure may cause acute radiation syndrome, a possibly fatal condition requiring effective therapy. Gut microbiota can be manipulated to fight against many diseases. We explored whether intestinal microbe transplantation could alleviate radiation‐induced toxicity. High‐throughput sequencing showed that gastrointestinal bacterial community composition differed between male and female mice and was associated with susceptibility to radiation toxicity. Faecal microbiota transplantation (FMT) increased the survival rate of irradiated animals, elevated peripheral white blood cell counts and improved gastrointestinal tract function and intestinal epithelial integrity in irradiated male and female mice. FMT preserved the intestinal bacterial composition and retained mRNA and long non‐coding RNA expression profiles of host small intestines in a sex‐specific fashion. Despite promoting angiogenesis, sex‐matched FMT did not accelerate the proliferation of cancer cells in vivo. FMT might serve as a therapeutic to mitigate radiation‐induced toxicity and improve the prognosis of tumour patients after radiotherapy. John Wiley and Sons Inc. 2017-02-27 2017-04 /pmc/articles/PMC5376756/ /pubmed/28242755 http://dx.doi.org/10.15252/emmm.201606932 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (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 | Research Articles Cui, Ming Xiao, Huiwen Li, Yuan Zhou, Lixin Zhao, Shuyi Luo, Dan Zheng, Qisheng Dong, Jiali Zhao, Yu Zhang, Xin Zhang, Junling Lu, Lu Wang, Haichao Fan, Saijun Faecal microbiota transplantation protects against radiation‐induced toxicity |
title | Faecal microbiota transplantation protects against radiation‐induced toxicity |
title_full | Faecal microbiota transplantation protects against radiation‐induced toxicity |
title_fullStr | Faecal microbiota transplantation protects against radiation‐induced toxicity |
title_full_unstemmed | Faecal microbiota transplantation protects against radiation‐induced toxicity |
title_short | Faecal microbiota transplantation protects against radiation‐induced toxicity |
title_sort | faecal microbiota transplantation protects against radiation‐induced toxicity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376756/ https://www.ncbi.nlm.nih.gov/pubmed/28242755 http://dx.doi.org/10.15252/emmm.201606932 |
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