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Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster

Loss of gut integrity is linked to various human diseases including inflammatory bowel disease. However, the mechanisms that lead to loss of barrier function remain poorly understood. Using D. melanogaster, we demonstrate that dietary restriction (DR) slows the age-related decline in intestinal inte...

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Autores principales: Akagi, Kazutaka, Wilson, Kenneth A., Katewa, Subhash D., Ortega, Mauricio, Simons, Jesse, Hilsabeck, Tyler A., Kapuria, Subir, Sharma, Amit, Jasper, Heinrich, Kapahi, Pankaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233930/
https://www.ncbi.nlm.nih.gov/pubmed/30383748
http://dx.doi.org/10.1371/journal.pgen.1007777
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author Akagi, Kazutaka
Wilson, Kenneth A.
Katewa, Subhash D.
Ortega, Mauricio
Simons, Jesse
Hilsabeck, Tyler A.
Kapuria, Subir
Sharma, Amit
Jasper, Heinrich
Kapahi, Pankaj
author_facet Akagi, Kazutaka
Wilson, Kenneth A.
Katewa, Subhash D.
Ortega, Mauricio
Simons, Jesse
Hilsabeck, Tyler A.
Kapuria, Subir
Sharma, Amit
Jasper, Heinrich
Kapahi, Pankaj
author_sort Akagi, Kazutaka
collection PubMed
description Loss of gut integrity is linked to various human diseases including inflammatory bowel disease. However, the mechanisms that lead to loss of barrier function remain poorly understood. Using D. melanogaster, we demonstrate that dietary restriction (DR) slows the age-related decline in intestinal integrity by enhancing enterocyte cellular fitness through up-regulation of dMyc in the intestinal epithelium. Reduction of dMyc in enterocytes induced cell death, which leads to increased gut permeability and reduced lifespan upon DR. Genetic mosaic and epistasis analyses suggest that cell competition, whereby neighboring cells eliminate unfit cells by apoptosis, mediates cell death in enterocytes with reduced levels of dMyc. We observed that enterocyte apoptosis was necessary for the increased gut permeability and shortened lifespan upon loss of dMyc. Furthermore, moderate activation of dMyc in the post-mitotic enteroblasts and enterocytes was sufficient to extend health-span on rich nutrient diets. We propose that dMyc acts as a barometer of enterocyte cell fitness impacting intestinal barrier function in response to changes in diet and age.
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spelling pubmed-62339302018-12-06 Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster Akagi, Kazutaka Wilson, Kenneth A. Katewa, Subhash D. Ortega, Mauricio Simons, Jesse Hilsabeck, Tyler A. Kapuria, Subir Sharma, Amit Jasper, Heinrich Kapahi, Pankaj PLoS Genet Research Article Loss of gut integrity is linked to various human diseases including inflammatory bowel disease. However, the mechanisms that lead to loss of barrier function remain poorly understood. Using D. melanogaster, we demonstrate that dietary restriction (DR) slows the age-related decline in intestinal integrity by enhancing enterocyte cellular fitness through up-regulation of dMyc in the intestinal epithelium. Reduction of dMyc in enterocytes induced cell death, which leads to increased gut permeability and reduced lifespan upon DR. Genetic mosaic and epistasis analyses suggest that cell competition, whereby neighboring cells eliminate unfit cells by apoptosis, mediates cell death in enterocytes with reduced levels of dMyc. We observed that enterocyte apoptosis was necessary for the increased gut permeability and shortened lifespan upon loss of dMyc. Furthermore, moderate activation of dMyc in the post-mitotic enteroblasts and enterocytes was sufficient to extend health-span on rich nutrient diets. We propose that dMyc acts as a barometer of enterocyte cell fitness impacting intestinal barrier function in response to changes in diet and age. Public Library of Science 2018-11-01 /pmc/articles/PMC6233930/ /pubmed/30383748 http://dx.doi.org/10.1371/journal.pgen.1007777 Text en © 2018 Akagi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Akagi, Kazutaka
Wilson, Kenneth A.
Katewa, Subhash D.
Ortega, Mauricio
Simons, Jesse
Hilsabeck, Tyler A.
Kapuria, Subir
Sharma, Amit
Jasper, Heinrich
Kapahi, Pankaj
Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title_full Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title_fullStr Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title_full_unstemmed Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title_short Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster
title_sort dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in d. melanogaster
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233930/
https://www.ncbi.nlm.nih.gov/pubmed/30383748
http://dx.doi.org/10.1371/journal.pgen.1007777
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