Cargando…
Cytoskeletal self-organization in neuromorphogenesis
Self-organization of dynamic microtubules via interactions with associated motors plays a critical role in spindle formation. The microtubule-based mechanisms underlying other aspects of cellular morphogenesis, such as the formation and development of protrusions from neuronal cells is less well und...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199815/ https://www.ncbi.nlm.nih.gov/pubmed/24847718 http://dx.doi.org/10.4161/bioa.29070 |
_version_ | 1782339979983192064 |
---|---|
author | Dehmelt, Leif |
author_facet | Dehmelt, Leif |
author_sort | Dehmelt, Leif |
collection | PubMed |
description | Self-organization of dynamic microtubules via interactions with associated motors plays a critical role in spindle formation. The microtubule-based mechanisms underlying other aspects of cellular morphogenesis, such as the formation and development of protrusions from neuronal cells is less well understood. In a recent study, we investigated the molecular mechanism that underlies the massive reorganization of microtubules induced in non-neuronal cells by expression of the neuronal microtubule stabilizer MAP2c. In that study we directly observed cortical dynein complexes and how they affect the dynamic behavior of motile microtubules in living cells. We found that stationary dynein complexes transiently associate with motile microtubules near the cell cortex and that their rapid turnover facilitates efficient microtubule transport. Here, we discuss our findings in the larger context of cellular morphogenesis with specific focus on self-organizing principles from which cellular shape patterns such as the thin protrusions of neurons can emerge. |
format | Online Article Text |
id | pubmed-4199815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-41998152015-03-04 Cytoskeletal self-organization in neuromorphogenesis Dehmelt, Leif Bioarchitecture Commentary Self-organization of dynamic microtubules via interactions with associated motors plays a critical role in spindle formation. The microtubule-based mechanisms underlying other aspects of cellular morphogenesis, such as the formation and development of protrusions from neuronal cells is less well understood. In a recent study, we investigated the molecular mechanism that underlies the massive reorganization of microtubules induced in non-neuronal cells by expression of the neuronal microtubule stabilizer MAP2c. In that study we directly observed cortical dynein complexes and how they affect the dynamic behavior of motile microtubules in living cells. We found that stationary dynein complexes transiently associate with motile microtubules near the cell cortex and that their rapid turnover facilitates efficient microtubule transport. Here, we discuss our findings in the larger context of cellular morphogenesis with specific focus on self-organizing principles from which cellular shape patterns such as the thin protrusions of neurons can emerge. Landes Bioscience 2014 2014-05-21 /pmc/articles/PMC4199815/ /pubmed/24847718 http://dx.doi.org/10.4161/bioa.29070 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Commentary Dehmelt, Leif Cytoskeletal self-organization in neuromorphogenesis |
title | Cytoskeletal self-organization in neuromorphogenesis |
title_full | Cytoskeletal self-organization in neuromorphogenesis |
title_fullStr | Cytoskeletal self-organization in neuromorphogenesis |
title_full_unstemmed | Cytoskeletal self-organization in neuromorphogenesis |
title_short | Cytoskeletal self-organization in neuromorphogenesis |
title_sort | cytoskeletal self-organization in neuromorphogenesis |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199815/ https://www.ncbi.nlm.nih.gov/pubmed/24847718 http://dx.doi.org/10.4161/bioa.29070 |
work_keys_str_mv | AT dehmeltleif cytoskeletalselforganizationinneuromorphogenesis |