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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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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. |
format | Online Article Text |
id | pubmed-4670727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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