‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis

Abstract In multicellular organisms cells compete for resources or growth factors. If any one cell type wins, the co-existence of diverse cell types disappears. Existing dynamic Flux Balance Analysis (dFBA) does not accommodate changes in cell density caused by competition. Therefore we here develop...

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Main Authors: Yanhua Liu, Hans V. Westerhoff
Format: Article
Language:English
Published: Nature Portfolio 2023-10-01
Series:npj Systems Biology and Applications
Online Access:https://doi.org/10.1038/s41540-023-00313-5
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author Yanhua Liu
Hans V. Westerhoff
author_facet Yanhua Liu
Hans V. Westerhoff
author_sort Yanhua Liu
collection DOAJ
description Abstract In multicellular organisms cells compete for resources or growth factors. If any one cell type wins, the co-existence of diverse cell types disappears. Existing dynamic Flux Balance Analysis (dFBA) does not accommodate changes in cell density caused by competition. Therefore we here develop ‘dynamic competition Flux Balance Analysis’ (dcFBA). With total biomass synthesis as objective, lower-growth-yield cells were outcompeted even when cells synthesized mutually required nutrients. Signal transduction between cells established co-existence, which suggests that such ‘socialness’ is required for multicellularity. Whilst mutants with increased specific growth rate did not outgrow the other cell types, loss of social characteristics did enable a mutant to outgrow the other cells. We discuss that ‘asocialness’ rather than enhanced growth rates, i.e., a reduced sensitivity to regulatory factors rather than enhanced growth rates, may characterize cancer cells and organisms causing ecological blooms. Therapies reinforcing cross-regulation may therefore be more effective than those targeting replication rates.
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spelling doaj.art-59701cf8180642b9ae6a6787733729a92023-10-29T12:27:52ZengNature Portfolionpj Systems Biology and Applications2056-71892023-10-019111310.1038/s41540-023-00313-5‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysisYanhua Liu0Hans V. Westerhoff1Swammerdam Institute for Life Sciences, University of AmsterdamSwammerdam Institute for Life Sciences, University of AmsterdamAbstract In multicellular organisms cells compete for resources or growth factors. If any one cell type wins, the co-existence of diverse cell types disappears. Existing dynamic Flux Balance Analysis (dFBA) does not accommodate changes in cell density caused by competition. Therefore we here develop ‘dynamic competition Flux Balance Analysis’ (dcFBA). With total biomass synthesis as objective, lower-growth-yield cells were outcompeted even when cells synthesized mutually required nutrients. Signal transduction between cells established co-existence, which suggests that such ‘socialness’ is required for multicellularity. Whilst mutants with increased specific growth rate did not outgrow the other cell types, loss of social characteristics did enable a mutant to outgrow the other cells. We discuss that ‘asocialness’ rather than enhanced growth rates, i.e., a reduced sensitivity to regulatory factors rather than enhanced growth rates, may characterize cancer cells and organisms causing ecological blooms. Therapies reinforcing cross-regulation may therefore be more effective than those targeting replication rates.https://doi.org/10.1038/s41540-023-00313-5
spellingShingle Yanhua Liu
Hans V. Westerhoff
‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
npj Systems Biology and Applications
title ‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
title_full ‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
title_fullStr ‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
title_full_unstemmed ‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
title_short ‘Social’ versus ‘asocial’ cells—dynamic competition flux balance analysis
title_sort social versus asocial cells dynamic competition flux balance analysis
url https://doi.org/10.1038/s41540-023-00313-5
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