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Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain

Radiotherapy is an effective tool in the treatment of malignant brain tumors. However, damage to brain stem and progenitor cells constitutes a major problem and is associated with long-term side effects. Autophagy has been shown to be involved in cell death, and the purpose of this study was to eval...

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Autores principales: Wang, Yafeng, Zhou, Kai, Li, Tao, Xu, Yiran, Xie, Cuicui, Sun, Yanyan, Zhang, Yaodong, Rodriguez, Juan, Blomgren, Klas, Zhu, Changlian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386526/
https://www.ncbi.nlm.nih.gov/pubmed/28333139
http://dx.doi.org/10.1038/cddis.2017.120
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author Wang, Yafeng
Zhou, Kai
Li, Tao
Xu, Yiran
Xie, Cuicui
Sun, Yanyan
Zhang, Yaodong
Rodriguez, Juan
Blomgren, Klas
Zhu, Changlian
author_facet Wang, Yafeng
Zhou, Kai
Li, Tao
Xu, Yiran
Xie, Cuicui
Sun, Yanyan
Zhang, Yaodong
Rodriguez, Juan
Blomgren, Klas
Zhu, Changlian
author_sort Wang, Yafeng
collection PubMed
description Radiotherapy is an effective tool in the treatment of malignant brain tumors. However, damage to brain stem and progenitor cells constitutes a major problem and is associated with long-term side effects. Autophagy has been shown to be involved in cell death, and the purpose of this study was to evaluate the effect of autophagy inhibition on neural stem and progenitor cell death in the juvenile brain. Ten-day-old selective Atg7 knockout (KO) mice and wild-type (WT) littermates were subjected to a single 6Gy dose of whole-brain irradiation. Cell death and proliferation as well as microglia activation and inflammation were evaluated in the dentate gyrus of the hippocampus and in the cerebellum at 6 h after irradiation. We found that cell death was reduced in Atg7 KO compared with WT mice at 6 h after irradiation. The number of activated microglia increased significantly in both the dentate gyrus and the cerebellum of WT mice after irradiation, but the increase was lower in the Atg7 KO mice. The levels of proinflammatory cytokines and chemokines decreased, especially in the cerebellum, in the Atg7 KO group. These results suggest that autophagy might be a potential target for preventing radiotherapy-induced neural stem and progenitor cell death and its associated long-term side effects.
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spelling pubmed-53865262017-04-27 Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain Wang, Yafeng Zhou, Kai Li, Tao Xu, Yiran Xie, Cuicui Sun, Yanyan Zhang, Yaodong Rodriguez, Juan Blomgren, Klas Zhu, Changlian Cell Death Dis Original Article Radiotherapy is an effective tool in the treatment of malignant brain tumors. However, damage to brain stem and progenitor cells constitutes a major problem and is associated with long-term side effects. Autophagy has been shown to be involved in cell death, and the purpose of this study was to evaluate the effect of autophagy inhibition on neural stem and progenitor cell death in the juvenile brain. Ten-day-old selective Atg7 knockout (KO) mice and wild-type (WT) littermates were subjected to a single 6Gy dose of whole-brain irradiation. Cell death and proliferation as well as microglia activation and inflammation were evaluated in the dentate gyrus of the hippocampus and in the cerebellum at 6 h after irradiation. We found that cell death was reduced in Atg7 KO compared with WT mice at 6 h after irradiation. The number of activated microglia increased significantly in both the dentate gyrus and the cerebellum of WT mice after irradiation, but the increase was lower in the Atg7 KO mice. The levels of proinflammatory cytokines and chemokines decreased, especially in the cerebellum, in the Atg7 KO group. These results suggest that autophagy might be a potential target for preventing radiotherapy-induced neural stem and progenitor cell death and its associated long-term side effects. Nature Publishing Group 2017-03 2017-03-23 /pmc/articles/PMC5386526/ /pubmed/28333139 http://dx.doi.org/10.1038/cddis.2017.120 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. 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 Original Article
Wang, Yafeng
Zhou, Kai
Li, Tao
Xu, Yiran
Xie, Cuicui
Sun, Yanyan
Zhang, Yaodong
Rodriguez, Juan
Blomgren, Klas
Zhu, Changlian
Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title_full Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title_fullStr Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title_full_unstemmed Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title_short Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
title_sort inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386526/
https://www.ncbi.nlm.nih.gov/pubmed/28333139
http://dx.doi.org/10.1038/cddis.2017.120
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