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Frequency modulation of ERK activation dynamics rewires cell fate

Transient versus sustained ERK MAP kinase (MAPK) activation dynamics induce proliferation versus differentiation in response to epidermal (EGF) or nerve (NGF) growth factors in PC‐12 cells. Duration of ERK activation has therefore been proposed to specify cell fate decisions. Using a biosensor to me...

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Autores principales: Ryu, Hyunryul, Chung, Minhwan, Dobrzyński, Maciej, Fey, Dirk, Blum, Yannick, Lee, Sung Sik, Peter, Matthias, Kholodenko, Boris N, Jeon, Noo Li, Pertz, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670727/
https://www.ncbi.nlm.nih.gov/pubmed/26613961
http://dx.doi.org/10.15252/msb.20156458
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author Ryu, Hyunryul
Chung, Minhwan
Dobrzyński, Maciej
Fey, Dirk
Blum, Yannick
Lee, Sung Sik
Peter, Matthias
Kholodenko, Boris N
Jeon, Noo Li
Pertz, Olivier
author_facet Ryu, Hyunryul
Chung, Minhwan
Dobrzyński, Maciej
Fey, Dirk
Blum, Yannick
Lee, Sung Sik
Peter, Matthias
Kholodenko, Boris N
Jeon, Noo Li
Pertz, Olivier
author_sort Ryu, Hyunryul
collection PubMed
description Transient versus sustained ERK MAP kinase (MAPK) activation dynamics induce proliferation versus differentiation in response to epidermal (EGF) or nerve (NGF) growth factors in PC‐12 cells. Duration of ERK activation has therefore been proposed to specify cell fate decisions. Using a biosensor to measure ERK activation dynamics in single living cells reveals that sustained EGF/NGF application leads to a heterogeneous mix of transient and sustained ERK activation dynamics in distinct cells of the population, different than the population average. EGF biases toward transient, while NGF biases toward sustained ERK activation responses. In contrast, pulsed growth factor application can repeatedly and homogeneously trigger ERK activity transients across the cell population. These datasets enable mathematical modeling to reveal salient features inherent to the MAPK network. Ultimately, this predicts pulsed growth factor stimulation regimes that can bypass the typical feedback activation to rewire the system toward cell differentiation irrespective of growth factor identity.
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spelling pubmed-46707272015-12-15 Frequency modulation of ERK activation dynamics rewires cell fate Ryu, Hyunryul Chung, Minhwan Dobrzyński, Maciej Fey, Dirk Blum, Yannick Lee, Sung Sik Peter, Matthias Kholodenko, Boris N Jeon, Noo Li Pertz, Olivier Mol Syst Biol Articles Transient versus sustained ERK MAP kinase (MAPK) activation dynamics induce proliferation versus differentiation in response to epidermal (EGF) or nerve (NGF) growth factors in PC‐12 cells. Duration of ERK activation has therefore been proposed to specify cell fate decisions. Using a biosensor to measure ERK activation dynamics in single living cells reveals that sustained EGF/NGF application leads to a heterogeneous mix of transient and sustained ERK activation dynamics in distinct cells of the population, different than the population average. EGF biases toward transient, while NGF biases toward sustained ERK activation responses. In contrast, pulsed growth factor application can repeatedly and homogeneously trigger ERK activity transients across the cell population. These datasets enable mathematical modeling to reveal salient features inherent to the MAPK network. Ultimately, this predicts pulsed growth factor stimulation regimes that can bypass the typical feedback activation to rewire the system toward cell differentiation irrespective of growth factor identity. John Wiley and Sons Inc. 2015-11-30 /pmc/articles/PMC4670727/ /pubmed/26613961 http://dx.doi.org/10.15252/msb.20156458 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Ryu, Hyunryul
Chung, Minhwan
Dobrzyński, Maciej
Fey, Dirk
Blum, Yannick
Lee, Sung Sik
Peter, Matthias
Kholodenko, Boris N
Jeon, Noo Li
Pertz, Olivier
Frequency modulation of ERK activation dynamics rewires cell fate
title Frequency modulation of ERK activation dynamics rewires cell fate
title_full Frequency modulation of ERK activation dynamics rewires cell fate
title_fullStr Frequency modulation of ERK activation dynamics rewires cell fate
title_full_unstemmed Frequency modulation of ERK activation dynamics rewires cell fate
title_short Frequency modulation of ERK activation dynamics rewires cell fate
title_sort frequency modulation of erk activation dynamics rewires cell fate
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670727/
https://www.ncbi.nlm.nih.gov/pubmed/26613961
http://dx.doi.org/10.15252/msb.20156458
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