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Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state
A yeast culture grown in a nutrient-rich medium initially containing 2% glucose is not limited in calorie supply. When yeast cells cultured in this medium consume glucose, they undergo cell cycle arrest at a checkpoint in late G1 and differentiate into quiescent and non-quiescent cell populations. S...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642482/ https://www.ncbi.nlm.nih.gov/pubmed/29050207 http://dx.doi.org/10.18632/oncotarget.20614 |
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author | Leonov, Anna Feldman, Rachel Piano, Amanda Arlia-Ciommo, Anthony Lutchman, Vicky Ahmadi, Masoumeh Elsaser, Sarah Fakim, Hana Heshmati-Moghaddam, Mahdi Hussain, Asimah Orfali, Sandra Rajen, Harshvardhan Roofigari-Esfahani, Negar Rosanelli, Leana Titorenko, Vladimir I. |
author_facet | Leonov, Anna Feldman, Rachel Piano, Amanda Arlia-Ciommo, Anthony Lutchman, Vicky Ahmadi, Masoumeh Elsaser, Sarah Fakim, Hana Heshmati-Moghaddam, Mahdi Hussain, Asimah Orfali, Sandra Rajen, Harshvardhan Roofigari-Esfahani, Negar Rosanelli, Leana Titorenko, Vladimir I. |
author_sort | Leonov, Anna |
collection | PubMed |
description | A yeast culture grown in a nutrient-rich medium initially containing 2% glucose is not limited in calorie supply. When yeast cells cultured in this medium consume glucose, they undergo cell cycle arrest at a checkpoint in late G1 and differentiate into quiescent and non-quiescent cell populations. Studies of such differentiation have provided insights into mechanisms of yeast chronological aging under conditions of excessive calorie intake. Caloric restriction is an aging-delaying dietary intervention. Here, we assessed how caloric restriction influences the differentiation of chronologically aging yeast cultures into quiescent and non-quiescent cells, and how it affects their properties. We found that caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of quiescence, entry into a non-quiescent state and survival in this state. Our findings suggest that caloric restriction delays yeast chronological aging by causing specific changes in the following: 1) a checkpoint in G1 for cell cycle arrest and entry into a quiescent state; 2) a growth phase in which high-density quiescent cells are committed to become low-density quiescent cells; 3) the differentiation of low-density quiescent cells into low-density non-quiescent cells; and 4) the conversion of high-density quiescent cells into high-density non-quiescent cells. |
format | Online Article Text |
id | pubmed-5642482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56424822017-10-18 Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state Leonov, Anna Feldman, Rachel Piano, Amanda Arlia-Ciommo, Anthony Lutchman, Vicky Ahmadi, Masoumeh Elsaser, Sarah Fakim, Hana Heshmati-Moghaddam, Mahdi Hussain, Asimah Orfali, Sandra Rajen, Harshvardhan Roofigari-Esfahani, Negar Rosanelli, Leana Titorenko, Vladimir I. Oncotarget Research Paper: Gerotarget (Focus on Aging) A yeast culture grown in a nutrient-rich medium initially containing 2% glucose is not limited in calorie supply. When yeast cells cultured in this medium consume glucose, they undergo cell cycle arrest at a checkpoint in late G1 and differentiate into quiescent and non-quiescent cell populations. Studies of such differentiation have provided insights into mechanisms of yeast chronological aging under conditions of excessive calorie intake. Caloric restriction is an aging-delaying dietary intervention. Here, we assessed how caloric restriction influences the differentiation of chronologically aging yeast cultures into quiescent and non-quiescent cells, and how it affects their properties. We found that caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of quiescence, entry into a non-quiescent state and survival in this state. Our findings suggest that caloric restriction delays yeast chronological aging by causing specific changes in the following: 1) a checkpoint in G1 for cell cycle arrest and entry into a quiescent state; 2) a growth phase in which high-density quiescent cells are committed to become low-density quiescent cells; 3) the differentiation of low-density quiescent cells into low-density non-quiescent cells; and 4) the conversion of high-density quiescent cells into high-density non-quiescent cells. Impact Journals LLC 2017-09-01 /pmc/articles/PMC5642482/ /pubmed/29050207 http://dx.doi.org/10.18632/oncotarget.20614 Text en Copyright: © 2017 Leonov et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Gerotarget (Focus on Aging) Leonov, Anna Feldman, Rachel Piano, Amanda Arlia-Ciommo, Anthony Lutchman, Vicky Ahmadi, Masoumeh Elsaser, Sarah Fakim, Hana Heshmati-Moghaddam, Mahdi Hussain, Asimah Orfali, Sandra Rajen, Harshvardhan Roofigari-Esfahani, Negar Rosanelli, Leana Titorenko, Vladimir I. Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title | Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title_full | Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title_fullStr | Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title_full_unstemmed | Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title_short | Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
title_sort | caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state |
topic | Research Paper: Gerotarget (Focus on Aging) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642482/ https://www.ncbi.nlm.nih.gov/pubmed/29050207 http://dx.doi.org/10.18632/oncotarget.20614 |
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