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The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport
Transport of membrane and cytosolic proteins into the primary cilium is essential for its role in cellular signaling. Using virtual three-dimensional superresolution light microscopy, the movements of membrane and soluble proteins from the cytoplasm to the primary cilium were mapped. In addition to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208104/ https://www.ncbi.nlm.nih.gov/pubmed/36857170 http://dx.doi.org/10.1091/mbc.E22-10-0452 |
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author | Ruba, Andrew Tingey, Mark Luo, Wangxi Yu, Jingjie Evangelou, Athanasios Higgins, Rachel Khim, Saovleak Yang, Weidong |
author_facet | Ruba, Andrew Tingey, Mark Luo, Wangxi Yu, Jingjie Evangelou, Athanasios Higgins, Rachel Khim, Saovleak Yang, Weidong |
author_sort | Ruba, Andrew |
collection | PubMed |
description | Transport of membrane and cytosolic proteins into the primary cilium is essential for its role in cellular signaling. Using virtual three-dimensional superresolution light microscopy, the movements of membrane and soluble proteins from the cytoplasm to the primary cilium were mapped. In addition to the well-characterized intraflagellar transport (IFT) route, we found two new pathways within the lumen of the primary cilium: passive diffusion and vesicle-assisted transport routes that are adopted by proteins for cytoplasm–cilium transport in live cells. Through these pathways, approximately half of IFT motors (KIF3A) and cargo (α-tubulin) take the passive diffusion route, and more than half of membrane-embedded G protein–coupled receptors (SSTR3 and HTR6) use RAB8A-regulated vesicles to transport into and inside primary cilia. Ciliary lumen transport is the preferred route for membrane proteins in the early stages of ciliogenesis, and inhibition of SSTR3 vesicle transport completely blocks ciliogenesis. Furthermore, clathrin-mediated, signal-dependent internalization of SSTR3 also occurs through the ciliary lumen. These transport routes were also observed in Chlamydomonas reinhardtii flagella, suggesting their conserved roles in trafficking of ciliary proteins. |
format | Online Article Text |
id | pubmed-10208104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-102081042023-07-20 The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport Ruba, Andrew Tingey, Mark Luo, Wangxi Yu, Jingjie Evangelou, Athanasios Higgins, Rachel Khim, Saovleak Yang, Weidong Mol Biol Cell Articles Transport of membrane and cytosolic proteins into the primary cilium is essential for its role in cellular signaling. Using virtual three-dimensional superresolution light microscopy, the movements of membrane and soluble proteins from the cytoplasm to the primary cilium were mapped. In addition to the well-characterized intraflagellar transport (IFT) route, we found two new pathways within the lumen of the primary cilium: passive diffusion and vesicle-assisted transport routes that are adopted by proteins for cytoplasm–cilium transport in live cells. Through these pathways, approximately half of IFT motors (KIF3A) and cargo (α-tubulin) take the passive diffusion route, and more than half of membrane-embedded G protein–coupled receptors (SSTR3 and HTR6) use RAB8A-regulated vesicles to transport into and inside primary cilia. Ciliary lumen transport is the preferred route for membrane proteins in the early stages of ciliogenesis, and inhibition of SSTR3 vesicle transport completely blocks ciliogenesis. Furthermore, clathrin-mediated, signal-dependent internalization of SSTR3 also occurs through the ciliary lumen. These transport routes were also observed in Chlamydomonas reinhardtii flagella, suggesting their conserved roles in trafficking of ciliary proteins. The American Society for Cell Biology 2023-05-05 /pmc/articles/PMC10208104/ /pubmed/36857170 http://dx.doi.org/10.1091/mbc.E22-10-0452 Text en © 2023 Ruba et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Ruba, Andrew Tingey, Mark Luo, Wangxi Yu, Jingjie Evangelou, Athanasios Higgins, Rachel Khim, Saovleak Yang, Weidong The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title | The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title_full | The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title_fullStr | The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title_full_unstemmed | The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title_short | The ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
title_sort | ciliary lumen accommodates passive diffusion and vesicle-assisted trafficking in cytoplasm–ciliary transport |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208104/ https://www.ncbi.nlm.nih.gov/pubmed/36857170 http://dx.doi.org/10.1091/mbc.E22-10-0452 |
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