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Caloric restriction delays yeast chronological aging by remodeling carbohydrate and lipid metabolism, altering peroxisomal and mitochondrial functionalities, and postponing the onsets of apoptotic and liponecrotic modes of regulated cell death

Anthony Arlia‐Ciommo, Anna Leonov, Adam Beach, Vincent R. Richard, Simon D. Bourque, Michelle T. Burstein, Pavlo Kyryakov, Alejandra Gomez-Perez, Olivia Koupaki, Rachel Feldman, Vladimir I. Titorenko

Oncotarget · 2018 · ▲ 20 citations

Abstract

// Anthony Arlia-Ciommo 1 , Anna Leonov 1 , Adam Beach 1 , Vincent R. Richard 1 , Simon D. Bourque 1 , Michelle T. Burstein 1 , Pavlo Kyryakov 1 , Alejandra Gomez-Perez 1 , Olivia Koupaki 1 , Rachel Feldman 1 and Vladimir I. Titorenko 1 1 Department of Biology, Concordia University, Montreal, Quebec, Canada Correspondence to: Vladimir I. Titorenko, email: [email protected] Keywords: yeast; cellular aging; caloric restriction(definition); metabolism; mitochondria Received: November 03, 2017      Accepted: February 25, 2018      Epub: March 05, 2018       Published: March 23, 2018 ABSTRACT A dietary regimen of caloric restriction delays aging in evolutionarily distant eukaryotes, including the budding yeast Saccharomyces cerevisiae . Here, we assessed how caloric restriction influences morphological, biochemical and cell biological properties of chronologically aging yeast advancing through different stages of the aging process. Our findings revealed that this low-calorie diet slows yeast chronological aging by mechanisms that coordinate the spatiotemporal dynamics of various cellular processes before entry into a non-proliferative state and after such entry. Caloric restriction causes a stepwise establishment of an aging-delaying cellular pattern by tuning a network that assimilates the following: 1) pathways of carbohydrate and lipid metabolism; 2) communications between the endoplasmic reticulum, lipid droplets, peroxisomes, mitochondria and the cytosol; and 3) a balance between the processes of mitochondrial fusion and fission. Through different phases of the aging process, the caloric restriction-dependent remodeling of this intricate network 1) postpones the age-related onsets of apoptotic and liponecrotic modes of regulated cell death; and 2) actively increases the chance of cell survival by supporting the maintenance of cellular proteostasis(definition). Because caloric restriction decreases the risk of cell death and actively increases the chance of cell survival throughout chronological lifespan, this dietary intervention extends longevity of chronologically aging yeast.

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OpenAlex
DOI
10.18632/oncotarget.24604
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2026-07-15 MST

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APA
Arlia‐Ciommo, A., Leonov, A., Beach, A., Richard, V.R., Bourque, S.D., Burstein, M.T., Kyryakov, P., Gomez-Perez, A., Koupaki, O., Feldman, R., &amp; Titorenko, V.I. (2018). Caloric restriction delays yeast chronological aging by remodeling carbohydrate and lipid metabolism, altering peroxisomal and mitochondrial functionalities, and postponing the onsets of apoptotic and liponecrotic modes of regulated cell death. <em>Oncotarget</em>. https://doi.org/10.18632/oncotarget.24604
Vancouver
Arlia‐Ciommo A, Leonov A, Beach A, Richard VR, Bourque SD, Burstein MT, et al. Caloric restriction delays yeast chronological aging by remodeling carbohydrate and lipid metabolism, altering peroxisomal and mitochondrial functionalities, and postponing the onsets of apoptotic and liponecrotic modes of regulated cell death. Oncotarget. 2018. doi:10.18632/oncotarget.24604.
BibTeX
@article{anthony2018Calori, title = {Caloric restriction delays yeast chronological aging by remodeling carbohydrate and lipid metabolism, altering peroxisomal and mitochondrial functionalities, and postponing the onsets of apoptotic and liponecrotic modes of regulated cell death}, author = {Anthony Arlia‐Ciommo and Anna Leonov and Adam Beach and Vincent R. Richard and Simon D. Bourque and Michelle T. Burstein and Pavlo Kyryakov and Alejandra Gomez-Perez and Olivia Koupaki and Rachel Feldman and Vladimir I. Titorenko}, journal = {Oncotarget}, year = {2018}, doi = {10.18632/oncotarget.24604}, }

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