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Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon

Bidirectional transport is a key issue in cellular biology. It requires coordination between microtubule-associated molecular motors that work in opposing directions. The major retrograde and anterograde motors involved in bidirectional transport are cytoplasmic dynein and conventional kinesin, resp...

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Autores principales: Segal, Michal, Soifer, Ilya, Petzold, Heike, Howard, Jonathon, Elbaum, Michael, Reiner, Orly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507287/
https://www.ncbi.nlm.nih.gov/pubmed/23213412
http://dx.doi.org/10.1242/bio.2012307
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author Segal, Michal
Soifer, Ilya
Petzold, Heike
Howard, Jonathon
Elbaum, Michael
Reiner, Orly
author_facet Segal, Michal
Soifer, Ilya
Petzold, Heike
Howard, Jonathon
Elbaum, Michael
Reiner, Orly
author_sort Segal, Michal
collection PubMed
description Bidirectional transport is a key issue in cellular biology. It requires coordination between microtubule-associated molecular motors that work in opposing directions. The major retrograde and anterograde motors involved in bidirectional transport are cytoplasmic dynein and conventional kinesin, respectively. It is clear that failures in molecular motor activity bear severe consequences, especially in the nervous system. Neuronal migration may be impaired during brain development, and impaired molecular motor activity in the adult is one of the hallmarks of neurodegenerative diseases leading to neuronal cell death. The mechanisms that regulate or coordinate kinesin and dynein activity to generate bidirectional transport of the same cargo are of utmost importance. We examined how Ndel1, a cytoplasmic dynein binding protein, may regulate non-vesicular bidirectional transport. Soluble Ndel1 protein, Ndel1-derived peptides or control proteins were mixed with fluorescent beads, injected into the squid giant axon, and the bead movements were recorded using time-lapse microscopy. Automated tracking allowed for extraction and unbiased analysis of a large data set. Beads moved in both directions with a clear bias to the anterograde direction. Velocities were distributed over a broad range and were typically slower than those associated with fast vesicle transport. Ironically, the main effect of Ndel1 and its derived peptides was an enhancement of anterograde motion. We propose that they may function primarily by inhibition of dynein-dependent resistance, which suggests that both dynein and kinesin motors may remain engaged with microtubules during bidirectional transport.
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spelling pubmed-35072872012-12-04 Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon Segal, Michal Soifer, Ilya Petzold, Heike Howard, Jonathon Elbaum, Michael Reiner, Orly Biol Open Research Article Bidirectional transport is a key issue in cellular biology. It requires coordination between microtubule-associated molecular motors that work in opposing directions. The major retrograde and anterograde motors involved in bidirectional transport are cytoplasmic dynein and conventional kinesin, respectively. It is clear that failures in molecular motor activity bear severe consequences, especially in the nervous system. Neuronal migration may be impaired during brain development, and impaired molecular motor activity in the adult is one of the hallmarks of neurodegenerative diseases leading to neuronal cell death. The mechanisms that regulate or coordinate kinesin and dynein activity to generate bidirectional transport of the same cargo are of utmost importance. We examined how Ndel1, a cytoplasmic dynein binding protein, may regulate non-vesicular bidirectional transport. Soluble Ndel1 protein, Ndel1-derived peptides or control proteins were mixed with fluorescent beads, injected into the squid giant axon, and the bead movements were recorded using time-lapse microscopy. Automated tracking allowed for extraction and unbiased analysis of a large data set. Beads moved in both directions with a clear bias to the anterograde direction. Velocities were distributed over a broad range and were typically slower than those associated with fast vesicle transport. Ironically, the main effect of Ndel1 and its derived peptides was an enhancement of anterograde motion. We propose that they may function primarily by inhibition of dynein-dependent resistance, which suggests that both dynein and kinesin motors may remain engaged with microtubules during bidirectional transport. The Company of Biologists 2012-01-06 /pmc/articles/PMC3507287/ /pubmed/23213412 http://dx.doi.org/10.1242/bio.2012307 Text en © 2012. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Article
Segal, Michal
Soifer, Ilya
Petzold, Heike
Howard, Jonathon
Elbaum, Michael
Reiner, Orly
Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title_full Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title_fullStr Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title_full_unstemmed Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title_short Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
title_sort ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507287/
https://www.ncbi.nlm.nih.gov/pubmed/23213412
http://dx.doi.org/10.1242/bio.2012307
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