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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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