Cargando…
Intraflagellar transport drives flagellar surface motility
The assembly and maintenance of all cilia and flagella require intraflagellar transport (IFT) along the axoneme. IFT has been implicated in sensory and motile ciliary functions, but the mechanisms of this relationship remain unclear. Here, we used Chlamydomonas flagellar surface motility (FSM) as a...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679542/ https://www.ncbi.nlm.nih.gov/pubmed/23795295 http://dx.doi.org/10.7554/eLife.00744 |
_version_ | 1782272989653368832 |
---|---|
author | Shih, Sheng Min Engel, Benjamin D Kocabas, Fatih Bilyard, Thomas Gennerich, Arne Marshall, Wallace F Yildiz, Ahmet |
author_facet | Shih, Sheng Min Engel, Benjamin D Kocabas, Fatih Bilyard, Thomas Gennerich, Arne Marshall, Wallace F Yildiz, Ahmet |
author_sort | Shih, Sheng Min |
collection | PubMed |
description | The assembly and maintenance of all cilia and flagella require intraflagellar transport (IFT) along the axoneme. IFT has been implicated in sensory and motile ciliary functions, but the mechanisms of this relationship remain unclear. Here, we used Chlamydomonas flagellar surface motility (FSM) as a model to test whether IFT provides force for gliding of cells across solid surfaces. We show that IFT trains are coupled to flagellar membrane glycoproteins (FMGs) in a Ca(2+)-dependent manner. IFT trains transiently pause through surface adhesion of their FMG cargos, and dynein-1b motors pull the cell towards the distal tip of the axoneme. Each train is transported by at least four motors, with only one type of motor active at a time. Our results demonstrate the mechanism of Chlamydomonas gliding motility and suggest that IFT plays a major role in adhesion-induced ciliary signaling pathways. DOI: http://dx.doi.org/10.7554/eLife.00744.001 |
format | Online Article Text |
id | pubmed-3679542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36795422013-06-21 Intraflagellar transport drives flagellar surface motility Shih, Sheng Min Engel, Benjamin D Kocabas, Fatih Bilyard, Thomas Gennerich, Arne Marshall, Wallace F Yildiz, Ahmet eLife Biophysics and Structural Biology The assembly and maintenance of all cilia and flagella require intraflagellar transport (IFT) along the axoneme. IFT has been implicated in sensory and motile ciliary functions, but the mechanisms of this relationship remain unclear. Here, we used Chlamydomonas flagellar surface motility (FSM) as a model to test whether IFT provides force for gliding of cells across solid surfaces. We show that IFT trains are coupled to flagellar membrane glycoproteins (FMGs) in a Ca(2+)-dependent manner. IFT trains transiently pause through surface adhesion of their FMG cargos, and dynein-1b motors pull the cell towards the distal tip of the axoneme. Each train is transported by at least four motors, with only one type of motor active at a time. Our results demonstrate the mechanism of Chlamydomonas gliding motility and suggest that IFT plays a major role in adhesion-induced ciliary signaling pathways. DOI: http://dx.doi.org/10.7554/eLife.00744.001 eLife Sciences Publications, Ltd 2013-06-11 /pmc/articles/PMC3679542/ /pubmed/23795295 http://dx.doi.org/10.7554/eLife.00744 Text en Copyright © 2013, Shih et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Shih, Sheng Min Engel, Benjamin D Kocabas, Fatih Bilyard, Thomas Gennerich, Arne Marshall, Wallace F Yildiz, Ahmet Intraflagellar transport drives flagellar surface motility |
title | Intraflagellar transport drives flagellar surface motility |
title_full | Intraflagellar transport drives flagellar surface motility |
title_fullStr | Intraflagellar transport drives flagellar surface motility |
title_full_unstemmed | Intraflagellar transport drives flagellar surface motility |
title_short | Intraflagellar transport drives flagellar surface motility |
title_sort | intraflagellar transport drives flagellar surface motility |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679542/ https://www.ncbi.nlm.nih.gov/pubmed/23795295 http://dx.doi.org/10.7554/eLife.00744 |
work_keys_str_mv | AT shihshengmin intraflagellartransportdrivesflagellarsurfacemotility AT engelbenjamind intraflagellartransportdrivesflagellarsurfacemotility AT kocabasfatih intraflagellartransportdrivesflagellarsurfacemotility AT bilyardthomas intraflagellartransportdrivesflagellarsurfacemotility AT gennericharne intraflagellartransportdrivesflagellarsurfacemotility AT marshallwallacef intraflagellartransportdrivesflagellarsurfacemotility AT yildizahmet intraflagellartransportdrivesflagellarsurfacemotility |