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Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding
The role of the primary cilium in key signaling pathways depends on dynamic regulation of ciliary membrane protein composition, yet we know little about the motors or membrane events that regulate ciliary membrane protein trafficking in existing organelles. Recently, we showed that cilium-generated...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362204/ https://www.ncbi.nlm.nih.gov/pubmed/25688564 http://dx.doi.org/10.7554/eLife.05242 |
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author | Cao, Muqing Ning, Jue Hernandez-Lara, Carmen I Belzile, Olivier Wang, Qian Dutcher, Susan K Liu, Yanjie Snell, William J |
author_facet | Cao, Muqing Ning, Jue Hernandez-Lara, Carmen I Belzile, Olivier Wang, Qian Dutcher, Susan K Liu, Yanjie Snell, William J |
author_sort | Cao, Muqing |
collection | PubMed |
description | The role of the primary cilium in key signaling pathways depends on dynamic regulation of ciliary membrane protein composition, yet we know little about the motors or membrane events that regulate ciliary membrane protein trafficking in existing organelles. Recently, we showed that cilium-generated signaling in Chlamydomonas induced rapid, anterograde IFT-independent, cytoplasmic microtubule-dependent redistribution of the membrane polypeptide, SAG1-C65, from the plasma membrane to the periciliary region and the ciliary membrane. Here, we report that the retrograde IFT motor, cytoplasmic dynein 1b, is required in the cytoplasm for this rapid redistribution. Furthermore, signaling-induced trafficking of SAG1-C65 into cilia is unidirectional and the entire complement of cellular SAG1-C65 is shed during signaling and can be recovered in the form of ciliary ectosomes that retain signal-inducing activity. Thus, during signaling, cells regulate ciliary membrane protein composition through cytoplasmic action of the retrograde IFT motor and shedding of ciliary ectosomes. DOI: http://dx.doi.org/10.7554/eLife.05242.001 |
format | Online Article Text |
id | pubmed-4362204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43622042015-03-18 Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding Cao, Muqing Ning, Jue Hernandez-Lara, Carmen I Belzile, Olivier Wang, Qian Dutcher, Susan K Liu, Yanjie Snell, William J eLife Cell Biology The role of the primary cilium in key signaling pathways depends on dynamic regulation of ciliary membrane protein composition, yet we know little about the motors or membrane events that regulate ciliary membrane protein trafficking in existing organelles. Recently, we showed that cilium-generated signaling in Chlamydomonas induced rapid, anterograde IFT-independent, cytoplasmic microtubule-dependent redistribution of the membrane polypeptide, SAG1-C65, from the plasma membrane to the periciliary region and the ciliary membrane. Here, we report that the retrograde IFT motor, cytoplasmic dynein 1b, is required in the cytoplasm for this rapid redistribution. Furthermore, signaling-induced trafficking of SAG1-C65 into cilia is unidirectional and the entire complement of cellular SAG1-C65 is shed during signaling and can be recovered in the form of ciliary ectosomes that retain signal-inducing activity. Thus, during signaling, cells regulate ciliary membrane protein composition through cytoplasmic action of the retrograde IFT motor and shedding of ciliary ectosomes. DOI: http://dx.doi.org/10.7554/eLife.05242.001 eLife Sciences Publications, Ltd 2015-02-17 /pmc/articles/PMC4362204/ /pubmed/25688564 http://dx.doi.org/10.7554/eLife.05242 Text en © 2015, Cao et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Cao, Muqing Ning, Jue Hernandez-Lara, Carmen I Belzile, Olivier Wang, Qian Dutcher, Susan K Liu, Yanjie Snell, William J Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title | Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title_full | Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title_fullStr | Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title_full_unstemmed | Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title_short | Uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde IFT motor and ciliary ectosome shedding |
title_sort | uni-directional ciliary membrane protein trafficking by a cytoplasmic retrograde ift motor and ciliary ectosome shedding |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362204/ https://www.ncbi.nlm.nih.gov/pubmed/25688564 http://dx.doi.org/10.7554/eLife.05242 |
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