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Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans

The response to osmotic stress is a highly conserved process for adapting to changing environmental conditions. Prior studies have shown that hyperosmolarity by addition of sorbitol to the growth medium is sufficient to increase both chronological and replicative lifespan in the budding yeast, Sacch...

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Autores principales: Chandler-Brown, Devon, Choi, Haeri, Park, Shirley, Ocampo, Billie R., Chen, Shiwen, Le, Anna, Sutphin, George L., Shamieh, Lara S., Smith, Erica D., Kaeberlein, Matt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621483/
https://www.ncbi.nlm.nih.gov/pubmed/26579191
http://dx.doi.org/10.3389/fgene.2015.00316
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author Chandler-Brown, Devon
Choi, Haeri
Park, Shirley
Ocampo, Billie R.
Chen, Shiwen
Le, Anna
Sutphin, George L.
Shamieh, Lara S.
Smith, Erica D.
Kaeberlein, Matt
author_facet Chandler-Brown, Devon
Choi, Haeri
Park, Shirley
Ocampo, Billie R.
Chen, Shiwen
Le, Anna
Sutphin, George L.
Shamieh, Lara S.
Smith, Erica D.
Kaeberlein, Matt
author_sort Chandler-Brown, Devon
collection PubMed
description The response to osmotic stress is a highly conserved process for adapting to changing environmental conditions. Prior studies have shown that hyperosmolarity by addition of sorbitol to the growth medium is sufficient to increase both chronological and replicative lifespan in the budding yeast, Saccharomyces cerevisiae. Here we report a similar phenomenon in the nematode Caenorhabditis elegans. Addition of sorbitol to the nematode growth medium induces an adaptive osmotic response and increases C. elegans lifespan by about 35%. Lifespan extension from 5% sorbitol behaves similarly to dietary restriction in a variety of genetic backgrounds, increasing lifespan additively with mutation of daf-2(e1370) and independently of daf-16(mu86), sir-2.1(ok434), aak-2(ok524), and hif-1(ia04). Dietary restriction by bacterial deprivation or mutation of eat-2(ad1113) fails to further extend lifespan in the presence of 5% sorbitol. Two mutants with constitutive activation of the osmotic response, osm-5(p813) and osm-7(n1515), were found to be long-lived, and lifespan extension from sorbitol required the glycerol biosynthetic enzymes GPDH-1 and GPDH-2. Taken together, these observations demonstrate that exposure to sorbitol at levels sufficient to induce an adaptive osmotic response extends lifespan in worms and define the osmotic stress response pathway as a longevity pathway conserved between yeast and nematodes.
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spelling pubmed-46214832015-11-17 Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans Chandler-Brown, Devon Choi, Haeri Park, Shirley Ocampo, Billie R. Chen, Shiwen Le, Anna Sutphin, George L. Shamieh, Lara S. Smith, Erica D. Kaeberlein, Matt Front Genet Genetics The response to osmotic stress is a highly conserved process for adapting to changing environmental conditions. Prior studies have shown that hyperosmolarity by addition of sorbitol to the growth medium is sufficient to increase both chronological and replicative lifespan in the budding yeast, Saccharomyces cerevisiae. Here we report a similar phenomenon in the nematode Caenorhabditis elegans. Addition of sorbitol to the nematode growth medium induces an adaptive osmotic response and increases C. elegans lifespan by about 35%. Lifespan extension from 5% sorbitol behaves similarly to dietary restriction in a variety of genetic backgrounds, increasing lifespan additively with mutation of daf-2(e1370) and independently of daf-16(mu86), sir-2.1(ok434), aak-2(ok524), and hif-1(ia04). Dietary restriction by bacterial deprivation or mutation of eat-2(ad1113) fails to further extend lifespan in the presence of 5% sorbitol. Two mutants with constitutive activation of the osmotic response, osm-5(p813) and osm-7(n1515), were found to be long-lived, and lifespan extension from sorbitol required the glycerol biosynthetic enzymes GPDH-1 and GPDH-2. Taken together, these observations demonstrate that exposure to sorbitol at levels sufficient to induce an adaptive osmotic response extends lifespan in worms and define the osmotic stress response pathway as a longevity pathway conserved between yeast and nematodes. Frontiers Media S.A. 2015-10-27 /pmc/articles/PMC4621483/ /pubmed/26579191 http://dx.doi.org/10.3389/fgene.2015.00316 Text en Copyright © 2015 Chandler-Brown, Choi, Park, Ocampo, Chen, Le, Sutphin, Shamieh, Smith and Kaeberlein. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Chandler-Brown, Devon
Choi, Haeri
Park, Shirley
Ocampo, Billie R.
Chen, Shiwen
Le, Anna
Sutphin, George L.
Shamieh, Lara S.
Smith, Erica D.
Kaeberlein, Matt
Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title_full Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title_fullStr Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title_full_unstemmed Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title_short Sorbitol treatment extends lifespan and induces the osmotic stress response in Caenorhabditis elegans
title_sort sorbitol treatment extends lifespan and induces the osmotic stress response in caenorhabditis elegans
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621483/
https://www.ncbi.nlm.nih.gov/pubmed/26579191
http://dx.doi.org/10.3389/fgene.2015.00316
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