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Entosis Is Induced by Glucose Starvation

Entosis is a mechanism of cell death that involves neighbor cell ingestion. This process occurs in cancers and promotes a form of cell competition, where winner cells engulf and kill losers. Entosis is driven by a mechanical differential that allows softer cells to eliminate stiffer cells. While thi...

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Detalles Bibliográficos
Autores principales: Hamann, Jens C., Surcel, Alexandra, Chen, Ruoyao, Teragawa, Carolyn, Albeck, John G., Robinson, Douglas N., Overholtzer, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559205/
https://www.ncbi.nlm.nih.gov/pubmed/28683313
http://dx.doi.org/10.1016/j.celrep.2017.06.037
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author Hamann, Jens C.
Surcel, Alexandra
Chen, Ruoyao
Teragawa, Carolyn
Albeck, John G.
Robinson, Douglas N.
Overholtzer, Michael
author_facet Hamann, Jens C.
Surcel, Alexandra
Chen, Ruoyao
Teragawa, Carolyn
Albeck, John G.
Robinson, Douglas N.
Overholtzer, Michael
author_sort Hamann, Jens C.
collection PubMed
description Entosis is a mechanism of cell death that involves neighbor cell ingestion. This process occurs in cancers and promotes a form of cell competition, where winner cells engulf and kill losers. Entosis is driven by a mechanical differential that allows softer cells to eliminate stiffer cells. While this process can be induced by matrix detachment, whether other stressors can activate entosis is unknown. Here, we find that entosis is induced in adherent cells by glucose withdrawal. Glucose withdrawal leads to a bimodal distribution of cells based on their deformability, where stiffer cells appear in a manner requiring the energy-sensing AMP-activated protein kinase (AMPK). We show that loser cells with high levels of AMPK activity are eliminated by winners through entosis, which supports winner cell proliferation under nutrient-deprived conditions. Our findings demonstrate that entosis serves as a cellular response to metabolic stress that enables nutrient recovery through neighbor cell ingestion.
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spelling pubmed-55592052017-08-16 Entosis Is Induced by Glucose Starvation Hamann, Jens C. Surcel, Alexandra Chen, Ruoyao Teragawa, Carolyn Albeck, John G. Robinson, Douglas N. Overholtzer, Michael Cell Rep Article Entosis is a mechanism of cell death that involves neighbor cell ingestion. This process occurs in cancers and promotes a form of cell competition, where winner cells engulf and kill losers. Entosis is driven by a mechanical differential that allows softer cells to eliminate stiffer cells. While this process can be induced by matrix detachment, whether other stressors can activate entosis is unknown. Here, we find that entosis is induced in adherent cells by glucose withdrawal. Glucose withdrawal leads to a bimodal distribution of cells based on their deformability, where stiffer cells appear in a manner requiring the energy-sensing AMP-activated protein kinase (AMPK). We show that loser cells with high levels of AMPK activity are eliminated by winners through entosis, which supports winner cell proliferation under nutrient-deprived conditions. Our findings demonstrate that entosis serves as a cellular response to metabolic stress that enables nutrient recovery through neighbor cell ingestion. 2017-07-05 /pmc/articles/PMC5559205/ /pubmed/28683313 http://dx.doi.org/10.1016/j.celrep.2017.06.037 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hamann, Jens C.
Surcel, Alexandra
Chen, Ruoyao
Teragawa, Carolyn
Albeck, John G.
Robinson, Douglas N.
Overholtzer, Michael
Entosis Is Induced by Glucose Starvation
title Entosis Is Induced by Glucose Starvation
title_full Entosis Is Induced by Glucose Starvation
title_fullStr Entosis Is Induced by Glucose Starvation
title_full_unstemmed Entosis Is Induced by Glucose Starvation
title_short Entosis Is Induced by Glucose Starvation
title_sort entosis is induced by glucose starvation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559205/
https://www.ncbi.nlm.nih.gov/pubmed/28683313
http://dx.doi.org/10.1016/j.celrep.2017.06.037
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