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Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation

Nutrients are vital to cellular activities, yet it is largely unknown how individual cells respond to nutrient deprivation. Live imaging results show that unlike the removal of amino acids or glutamine that immediately halts cell cycle progression, glucose withdrawal does not prevent cells from comp...

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Detalles Bibliográficos
Autores principales: Zheng, Dianpeng, Mao, Yaowen, Gao, Yinglong, He, Feng, Ma, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359942/
https://www.ncbi.nlm.nih.gov/pubmed/37485365
http://dx.doi.org/10.1016/j.isci.2023.107198
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author Zheng, Dianpeng
Mao, Yaowen
Gao, Yinglong
He, Feng
Ma, Jun
author_facet Zheng, Dianpeng
Mao, Yaowen
Gao, Yinglong
He, Feng
Ma, Jun
author_sort Zheng, Dianpeng
collection PubMed
description Nutrients are vital to cellular activities, yet it is largely unknown how individual cells respond to nutrient deprivation. Live imaging results show that unlike the removal of amino acids or glutamine that immediately halts cell cycle progression, glucose withdrawal does not prevent cells from completing their current cycle. Although cells that begin to experience glucose withdrawal in S phase give rise to daughter cells with an equal choice of proliferation or quiescence, those enduring such experience in G1 phase give rise to daughter cells that predominantly enter quiescence. This fate choice difference stems from p21 protein accumulated during G2/M of the latter cells. Induced degradation of p21 permits daughter cells to enter S phase but with a consequent accumulation of DNA damage. These results suggest that mother cells that begin to experience glucose limitation in G1 phase take preemptive steps toward preventing daughter cells from making a harmful choice.
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spelling pubmed-103599422023-07-22 Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation Zheng, Dianpeng Mao, Yaowen Gao, Yinglong He, Feng Ma, Jun iScience Article Nutrients are vital to cellular activities, yet it is largely unknown how individual cells respond to nutrient deprivation. Live imaging results show that unlike the removal of amino acids or glutamine that immediately halts cell cycle progression, glucose withdrawal does not prevent cells from completing their current cycle. Although cells that begin to experience glucose withdrawal in S phase give rise to daughter cells with an equal choice of proliferation or quiescence, those enduring such experience in G1 phase give rise to daughter cells that predominantly enter quiescence. This fate choice difference stems from p21 protein accumulated during G2/M of the latter cells. Induced degradation of p21 permits daughter cells to enter S phase but with a consequent accumulation of DNA damage. These results suggest that mother cells that begin to experience glucose limitation in G1 phase take preemptive steps toward preventing daughter cells from making a harmful choice. Elsevier 2023-06-24 /pmc/articles/PMC10359942/ /pubmed/37485365 http://dx.doi.org/10.1016/j.isci.2023.107198 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zheng, Dianpeng
Mao, Yaowen
Gao, Yinglong
He, Feng
Ma, Jun
Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title_full Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title_fullStr Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title_full_unstemmed Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title_short Daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
title_sort daughter cell fate choice instructed preemptively by mother cells facing nutrient limitation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359942/
https://www.ncbi.nlm.nih.gov/pubmed/37485365
http://dx.doi.org/10.1016/j.isci.2023.107198
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