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Wave patterns organize cellular protrusions and control cortical dynamics
Cellular protrusions are typically considered as distinct structures associated with specific regulators. However, we found that these regulators coordinately localize as propagating cortical waves, suggesting a common underlying mechanism. These molecular events fell into two excitable networks, th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413885/ https://www.ncbi.nlm.nih.gov/pubmed/30858181 http://dx.doi.org/10.15252/msb.20188585 |
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author | Miao, Yuchuan Bhattacharya, Sayak Banerjee, Tatsat Abubaker‐Sharif, Bedri Long, Yu Inoue, Takanari Iglesias, Pablo A Devreotes, Peter N |
author_facet | Miao, Yuchuan Bhattacharya, Sayak Banerjee, Tatsat Abubaker‐Sharif, Bedri Long, Yu Inoue, Takanari Iglesias, Pablo A Devreotes, Peter N |
author_sort | Miao, Yuchuan |
collection | PubMed |
description | Cellular protrusions are typically considered as distinct structures associated with specific regulators. However, we found that these regulators coordinately localize as propagating cortical waves, suggesting a common underlying mechanism. These molecular events fell into two excitable networks, the signal transduction network STEN and the cytoskeletal network CEN with different wave substructures. Computational studies using a coupled‐network model reproduced these features and showed that the morphology and kinetics of the waves depended on strengths of feedback loops. Chemically induced dimerization at multiple nodes produced distinct, coordinated alterations in patterns of other network components. Taken together, these studies indicate: STEN positive feedback is mediated by mutual inhibition between Ras/Rap and PIP2, while negative feedback depends on delayed PKB activation; PKBs link STEN to CEN; CEN includes positive feedback between Rac and F‐actin, and exerts fast positive and slow negative feedbacks to STEN. The alterations produced protrusions resembling filopodia, ruffles, pseudopodia, or lamellipodia, suggesting that these structures arise from a common regulatory mechanism and that the overall state of the STEN‐CEN system determines cellular morphology. |
format | Online Article Text |
id | pubmed-6413885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64138852019-03-22 Wave patterns organize cellular protrusions and control cortical dynamics Miao, Yuchuan Bhattacharya, Sayak Banerjee, Tatsat Abubaker‐Sharif, Bedri Long, Yu Inoue, Takanari Iglesias, Pablo A Devreotes, Peter N Mol Syst Biol Articles Cellular protrusions are typically considered as distinct structures associated with specific regulators. However, we found that these regulators coordinately localize as propagating cortical waves, suggesting a common underlying mechanism. These molecular events fell into two excitable networks, the signal transduction network STEN and the cytoskeletal network CEN with different wave substructures. Computational studies using a coupled‐network model reproduced these features and showed that the morphology and kinetics of the waves depended on strengths of feedback loops. Chemically induced dimerization at multiple nodes produced distinct, coordinated alterations in patterns of other network components. Taken together, these studies indicate: STEN positive feedback is mediated by mutual inhibition between Ras/Rap and PIP2, while negative feedback depends on delayed PKB activation; PKBs link STEN to CEN; CEN includes positive feedback between Rac and F‐actin, and exerts fast positive and slow negative feedbacks to STEN. The alterations produced protrusions resembling filopodia, ruffles, pseudopodia, or lamellipodia, suggesting that these structures arise from a common regulatory mechanism and that the overall state of the STEN‐CEN system determines cellular morphology. John Wiley and Sons Inc. 2019-03-12 /pmc/articles/PMC6413885/ /pubmed/30858181 http://dx.doi.org/10.15252/msb.20188585 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the 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 Miao, Yuchuan Bhattacharya, Sayak Banerjee, Tatsat Abubaker‐Sharif, Bedri Long, Yu Inoue, Takanari Iglesias, Pablo A Devreotes, Peter N Wave patterns organize cellular protrusions and control cortical dynamics |
title | Wave patterns organize cellular protrusions and control cortical dynamics |
title_full | Wave patterns organize cellular protrusions and control cortical dynamics |
title_fullStr | Wave patterns organize cellular protrusions and control cortical dynamics |
title_full_unstemmed | Wave patterns organize cellular protrusions and control cortical dynamics |
title_short | Wave patterns organize cellular protrusions and control cortical dynamics |
title_sort | wave patterns organize cellular protrusions and control cortical dynamics |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413885/ https://www.ncbi.nlm.nih.gov/pubmed/30858181 http://dx.doi.org/10.15252/msb.20188585 |
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