Cargando…

Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila

Exposure to genotoxic stress by environmental agents or treatments, such as radiation therapy, can diminish healthspan and accelerate aging. We have developed a Drosophila melanogaster model to study the molecular effects of radiation-induced damage and repair. Utilizing a quantitative intestinal pe...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharma, Amit, Akagi, Kazutaka, Pattavina, Blaine, Wilson, Kenneth A., Nelson, Christopher, Watson, Mark, Maksoud, Elie, Harata, Ayano, Ortega, Mauricio, Brem, Rachel B., Kapahi, Pankaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644626/
https://www.ncbi.nlm.nih.gov/pubmed/33154387
http://dx.doi.org/10.1038/s41598-020-75867-z
_version_ 1783606493423075328
author Sharma, Amit
Akagi, Kazutaka
Pattavina, Blaine
Wilson, Kenneth A.
Nelson, Christopher
Watson, Mark
Maksoud, Elie
Harata, Ayano
Ortega, Mauricio
Brem, Rachel B.
Kapahi, Pankaj
author_facet Sharma, Amit
Akagi, Kazutaka
Pattavina, Blaine
Wilson, Kenneth A.
Nelson, Christopher
Watson, Mark
Maksoud, Elie
Harata, Ayano
Ortega, Mauricio
Brem, Rachel B.
Kapahi, Pankaj
author_sort Sharma, Amit
collection PubMed
description Exposure to genotoxic stress by environmental agents or treatments, such as radiation therapy, can diminish healthspan and accelerate aging. We have developed a Drosophila melanogaster model to study the molecular effects of radiation-induced damage and repair. Utilizing a quantitative intestinal permeability assay, we performed an unbiased GWAS screen (using 156 strains from the Drosophila Genetic Reference Panel) to search for natural genetic variants that regulate radiation-induced gut permeability in adult D. melanogaster. From this screen, we identified an RNA binding protein, Musashi (msi), as one of the possible genes associated with changes in intestinal permeability upon radiation. The overexpression of msi promoted intestinal stem cell proliferation, which increased survival after irradiation and rescued radiation-induced intestinal permeability. In summary, we have established D. melanogaster as an expedient model system to study the effects of radiation-induced damage to the intestine in adults and have identified msi as a potential therapeutic target.
format Online
Article
Text
id pubmed-7644626
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-76446262020-11-06 Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila Sharma, Amit Akagi, Kazutaka Pattavina, Blaine Wilson, Kenneth A. Nelson, Christopher Watson, Mark Maksoud, Elie Harata, Ayano Ortega, Mauricio Brem, Rachel B. Kapahi, Pankaj Sci Rep Article Exposure to genotoxic stress by environmental agents or treatments, such as radiation therapy, can diminish healthspan and accelerate aging. We have developed a Drosophila melanogaster model to study the molecular effects of radiation-induced damage and repair. Utilizing a quantitative intestinal permeability assay, we performed an unbiased GWAS screen (using 156 strains from the Drosophila Genetic Reference Panel) to search for natural genetic variants that regulate radiation-induced gut permeability in adult D. melanogaster. From this screen, we identified an RNA binding protein, Musashi (msi), as one of the possible genes associated with changes in intestinal permeability upon radiation. The overexpression of msi promoted intestinal stem cell proliferation, which increased survival after irradiation and rescued radiation-induced intestinal permeability. In summary, we have established D. melanogaster as an expedient model system to study the effects of radiation-induced damage to the intestine in adults and have identified msi as a potential therapeutic target. Nature Publishing Group UK 2020-11-05 /pmc/articles/PMC7644626/ /pubmed/33154387 http://dx.doi.org/10.1038/s41598-020-75867-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sharma, Amit
Akagi, Kazutaka
Pattavina, Blaine
Wilson, Kenneth A.
Nelson, Christopher
Watson, Mark
Maksoud, Elie
Harata, Ayano
Ortega, Mauricio
Brem, Rachel B.
Kapahi, Pankaj
Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title_full Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title_fullStr Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title_full_unstemmed Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title_short Musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in Drosophila
title_sort musashi expression in intestinal stem cells attenuates radiation-induced decline in intestinal permeability and survival in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644626/
https://www.ncbi.nlm.nih.gov/pubmed/33154387
http://dx.doi.org/10.1038/s41598-020-75867-z
work_keys_str_mv AT sharmaamit musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT akagikazutaka musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT pattavinablaine musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT wilsonkennetha musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT nelsonchristopher musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT watsonmark musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT maksoudelie musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT harataayano musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT ortegamauricio musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT bremrachelb musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila
AT kapahipankaj musashiexpressioninintestinalstemcellsattenuatesradiationinduceddeclineinintestinalpermeabilityandsurvivalindrosophila