Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Muqing, Ning, Jue, Hernandez-Lara, Carmen I, Belzile, Olivier, Wang, Qian, Dutcher, Susan K, Liu, Yanjie, Snell, William J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
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
_version_ 1782361779562610688
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
work_keys_str_mv AT caomuqing unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT ningjue unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT hernandezlaracarmeni unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT belzileolivier unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT wangqian unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT dutchersusank unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT liuyanjie unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding
AT snellwilliamj unidirectionalciliarymembraneproteintraffickingbyacytoplasmicretrogradeiftmotorandciliaryectosomeshedding