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Triggering signaling pathways using F-actin self-organization
The spatiotemporal organization of proteins within cells is essential for cell fate behavior. Although it is known that the cytoskeleton is vital for numerous cellular functions, it remains unclear how cytoskeletal activity can shape and control signaling pathways in space and time throughout the ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048156/ https://www.ncbi.nlm.nih.gov/pubmed/27698406 http://dx.doi.org/10.1038/srep34657 |
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author | Colin, A. Bonnemay, L. Gayrard, C. Gautier, J. Gueroui, Z. |
author_facet | Colin, A. Bonnemay, L. Gayrard, C. Gautier, J. Gueroui, Z. |
author_sort | Colin, A. |
collection | PubMed |
description | The spatiotemporal organization of proteins within cells is essential for cell fate behavior. Although it is known that the cytoskeleton is vital for numerous cellular functions, it remains unclear how cytoskeletal activity can shape and control signaling pathways in space and time throughout the cell cytoplasm. Here we show that F-actin self-organization can trigger signaling pathways by engineering two novel properties of the microfilament self-organization: (1) the confinement of signaling proteins and (2) their scaffolding along actin polymers. Using in vitro reconstitutions of cellular functions, we found that both the confinement of nanoparticle-based signaling platforms powered by F-actin contractility and the scaffolding of engineered signaling proteins along actin microfilaments can drive a signaling switch. Using Ran-dependent microtubule nucleation, we found that F-actin dynamics promotes the robust assembly of microtubules. Our in vitro assay is a first step towards the development of novel bottom-up strategies to decipher the interplay between cytoskeleton spatial organization and signaling pathway activity. |
format | Online Article Text |
id | pubmed-5048156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50481562016-10-11 Triggering signaling pathways using F-actin self-organization Colin, A. Bonnemay, L. Gayrard, C. Gautier, J. Gueroui, Z. Sci Rep Article The spatiotemporal organization of proteins within cells is essential for cell fate behavior. Although it is known that the cytoskeleton is vital for numerous cellular functions, it remains unclear how cytoskeletal activity can shape and control signaling pathways in space and time throughout the cell cytoplasm. Here we show that F-actin self-organization can trigger signaling pathways by engineering two novel properties of the microfilament self-organization: (1) the confinement of signaling proteins and (2) their scaffolding along actin polymers. Using in vitro reconstitutions of cellular functions, we found that both the confinement of nanoparticle-based signaling platforms powered by F-actin contractility and the scaffolding of engineered signaling proteins along actin microfilaments can drive a signaling switch. Using Ran-dependent microtubule nucleation, we found that F-actin dynamics promotes the robust assembly of microtubules. Our in vitro assay is a first step towards the development of novel bottom-up strategies to decipher the interplay between cytoskeleton spatial organization and signaling pathway activity. Nature Publishing Group 2016-10-04 /pmc/articles/PMC5048156/ /pubmed/27698406 http://dx.doi.org/10.1038/srep34657 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Colin, A. Bonnemay, L. Gayrard, C. Gautier, J. Gueroui, Z. Triggering signaling pathways using F-actin self-organization |
title | Triggering signaling pathways using F-actin self-organization |
title_full | Triggering signaling pathways using F-actin self-organization |
title_fullStr | Triggering signaling pathways using F-actin self-organization |
title_full_unstemmed | Triggering signaling pathways using F-actin self-organization |
title_short | Triggering signaling pathways using F-actin self-organization |
title_sort | triggering signaling pathways using f-actin self-organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048156/ https://www.ncbi.nlm.nih.gov/pubmed/27698406 http://dx.doi.org/10.1038/srep34657 |
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