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Processive flow by biased polymerization mediates the slow axonal transport of actin

Classic pulse-chase studies have shown that actin is conveyed in slow axonal transport, but the mechanistic basis for this movement is unknown. Recently, we reported that axonal actin was surprisingly dynamic, with focal assembly/disassembly events (“actin hotspots”) and elongating polymers along th...

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Detalles Bibliográficos
Autores principales: Chakrabarty, Nilaj, Dubey, Pankaj, Tang, Yong, Ganguly, Archan, Ladt, Kelsey, Leterrier, Christophe, Jung, Peter, Roy, Subhojit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314539/
https://www.ncbi.nlm.nih.gov/pubmed/30401699
http://dx.doi.org/10.1083/jcb.201711022
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author Chakrabarty, Nilaj
Dubey, Pankaj
Tang, Yong
Ganguly, Archan
Ladt, Kelsey
Leterrier, Christophe
Jung, Peter
Roy, Subhojit
author_facet Chakrabarty, Nilaj
Dubey, Pankaj
Tang, Yong
Ganguly, Archan
Ladt, Kelsey
Leterrier, Christophe
Jung, Peter
Roy, Subhojit
author_sort Chakrabarty, Nilaj
collection PubMed
description Classic pulse-chase studies have shown that actin is conveyed in slow axonal transport, but the mechanistic basis for this movement is unknown. Recently, we reported that axonal actin was surprisingly dynamic, with focal assembly/disassembly events (“actin hotspots”) and elongating polymers along the axon shaft (“actin trails”). Using a combination of live imaging, superresolution microscopy, and modeling, in this study, we explore how these dynamic structures can lead to processive transport of actin. We found relatively more actin trails elongated anterogradely as well as an overall slow, anterogradely biased flow of actin in axon shafts. Starting with first principles of monomer/filament assembly and incorporating imaging data, we generated a quantitative model simulating axonal hotspots and trails. Our simulations predict that the axonal actin dynamics indeed lead to a slow anterogradely biased flow of the population. Collectively, the data point to a surprising scenario where local assembly and biased polymerization generate the slow axonal transport of actin without involvement of microtubules (MTs) or MT-based motors. Mechanistically distinct from polymer sliding, this might be a general strategy to convey highly dynamic cytoskeletal cargoes.
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spelling pubmed-63145392019-07-07 Processive flow by biased polymerization mediates the slow axonal transport of actin Chakrabarty, Nilaj Dubey, Pankaj Tang, Yong Ganguly, Archan Ladt, Kelsey Leterrier, Christophe Jung, Peter Roy, Subhojit J Cell Biol Research Articles Classic pulse-chase studies have shown that actin is conveyed in slow axonal transport, but the mechanistic basis for this movement is unknown. Recently, we reported that axonal actin was surprisingly dynamic, with focal assembly/disassembly events (“actin hotspots”) and elongating polymers along the axon shaft (“actin trails”). Using a combination of live imaging, superresolution microscopy, and modeling, in this study, we explore how these dynamic structures can lead to processive transport of actin. We found relatively more actin trails elongated anterogradely as well as an overall slow, anterogradely biased flow of actin in axon shafts. Starting with first principles of monomer/filament assembly and incorporating imaging data, we generated a quantitative model simulating axonal hotspots and trails. Our simulations predict that the axonal actin dynamics indeed lead to a slow anterogradely biased flow of the population. Collectively, the data point to a surprising scenario where local assembly and biased polymerization generate the slow axonal transport of actin without involvement of microtubules (MTs) or MT-based motors. Mechanistically distinct from polymer sliding, this might be a general strategy to convey highly dynamic cytoskeletal cargoes. Rockefeller University Press 2019-01-07 /pmc/articles/PMC6314539/ /pubmed/30401699 http://dx.doi.org/10.1083/jcb.201711022 Text en © 2018 Chakrabarty et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Chakrabarty, Nilaj
Dubey, Pankaj
Tang, Yong
Ganguly, Archan
Ladt, Kelsey
Leterrier, Christophe
Jung, Peter
Roy, Subhojit
Processive flow by biased polymerization mediates the slow axonal transport of actin
title Processive flow by biased polymerization mediates the slow axonal transport of actin
title_full Processive flow by biased polymerization mediates the slow axonal transport of actin
title_fullStr Processive flow by biased polymerization mediates the slow axonal transport of actin
title_full_unstemmed Processive flow by biased polymerization mediates the slow axonal transport of actin
title_short Processive flow by biased polymerization mediates the slow axonal transport of actin
title_sort processive flow by biased polymerization mediates the slow axonal transport of actin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314539/
https://www.ncbi.nlm.nih.gov/pubmed/30401699
http://dx.doi.org/10.1083/jcb.201711022
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