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Tracking of plus-ends reveals microtubule functional diversity in different cell types
Many cellular processes are tightly connected to the dynamics of microtubules (MTs). While in neuronal axons MTs mainly regulate intracellular trafficking, they participate in cytoskeleton reorganization in many other eukaryotic cells, enabling the cell to efficiently adapt to changes in the environ...
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/PMC4962100/ https://www.ncbi.nlm.nih.gov/pubmed/27461361 http://dx.doi.org/10.1038/srep30285 |
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author | Shaebani, M. Reza Pasula, Aravind Ott, Albrecht Santen, Ludger |
author_facet | Shaebani, M. Reza Pasula, Aravind Ott, Albrecht Santen, Ludger |
author_sort | Shaebani, M. Reza |
collection | PubMed |
description | Many cellular processes are tightly connected to the dynamics of microtubules (MTs). While in neuronal axons MTs mainly regulate intracellular trafficking, they participate in cytoskeleton reorganization in many other eukaryotic cells, enabling the cell to efficiently adapt to changes in the environment. We show that the functional differences of MTs in different cell types and regions is reflected in the dynamic properties of MT tips. Using plus-end tracking proteins EB1 to monitor growing MT plus-ends, we show that MT dynamics and life cycle in axons of human neurons significantly differ from that of fibroblast cells. The density of plus-ends, as well as the rescue and catastrophe frequencies increase while the growth rate decreases toward the fibroblast cell margin. This results in a rather stable filamentous network structure and maintains the connection between nucleus and membrane. In contrast, plus-ends are uniformly distributed along the axons and exhibit diverse polymerization run times and spatially homogeneous rescue and catastrophe frequencies, leading to MT segments of various lengths. The probability distributions of the excursion length of polymerization and the MT length both follow nearly exponential tails, in agreement with the analytical predictions of a two-state model of MT dynamics. |
format | Online Article Text |
id | pubmed-4962100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49621002016-08-08 Tracking of plus-ends reveals microtubule functional diversity in different cell types Shaebani, M. Reza Pasula, Aravind Ott, Albrecht Santen, Ludger Sci Rep Article Many cellular processes are tightly connected to the dynamics of microtubules (MTs). While in neuronal axons MTs mainly regulate intracellular trafficking, they participate in cytoskeleton reorganization in many other eukaryotic cells, enabling the cell to efficiently adapt to changes in the environment. We show that the functional differences of MTs in different cell types and regions is reflected in the dynamic properties of MT tips. Using plus-end tracking proteins EB1 to monitor growing MT plus-ends, we show that MT dynamics and life cycle in axons of human neurons significantly differ from that of fibroblast cells. The density of plus-ends, as well as the rescue and catastrophe frequencies increase while the growth rate decreases toward the fibroblast cell margin. This results in a rather stable filamentous network structure and maintains the connection between nucleus and membrane. In contrast, plus-ends are uniformly distributed along the axons and exhibit diverse polymerization run times and spatially homogeneous rescue and catastrophe frequencies, leading to MT segments of various lengths. The probability distributions of the excursion length of polymerization and the MT length both follow nearly exponential tails, in agreement with the analytical predictions of a two-state model of MT dynamics. Nature Publishing Group 2016-07-27 /pmc/articles/PMC4962100/ /pubmed/27461361 http://dx.doi.org/10.1038/srep30285 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 Shaebani, M. Reza Pasula, Aravind Ott, Albrecht Santen, Ludger Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title | Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title_full | Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title_fullStr | Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title_full_unstemmed | Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title_short | Tracking of plus-ends reveals microtubule functional diversity in different cell types |
title_sort | tracking of plus-ends reveals microtubule functional diversity in different cell types |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962100/ https://www.ncbi.nlm.nih.gov/pubmed/27461361 http://dx.doi.org/10.1038/srep30285 |
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