Cargando…
Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of...
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/PMC3736543/ https://www.ncbi.nlm.nih.gov/pubmed/23930224 http://dx.doi.org/10.7554/eLife.00654 |
_version_ | 1782279774556651520 |
---|---|
author | Ye, Fan Breslow, David K Koslover, Elena F Spakowitz, Andrew J Nelson, W James Nachury, Maxence V |
author_facet | Ye, Fan Breslow, David K Koslover, Elena F Spakowitz, Andrew J Nelson, W James Nachury, Maxence V |
author_sort | Ye, Fan |
collection | PubMed |
description | The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of Somatostatin Receptor 3 (SSTR3, a GPCR) and Smoothened (Smo, a Hedgehog signal transducer) in the ciliary membrane. While IFT trains moved processively from one end of the cilium to the other, single SSTR3 and Smo underwent mostly diffusive behavior interspersed with short periods of directional movements. Statistical subtraction of instant velocities revealed that SSTR3 and Smo spent less than a third of their time undergoing active transport. Finally, SSTR3 and IFT movements could be uncoupled by perturbing either membrane protein diffusion or active transport. Thus ciliary membrane proteins move predominantly by diffusion, and attachment to IFT trains is transient and stochastic rather than processive or spatially determined. DOI: http://dx.doi.org/10.7554/eLife.00654.001 |
format | Online Article Text |
id | pubmed-3736543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37365432013-08-08 Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors Ye, Fan Breslow, David K Koslover, Elena F Spakowitz, Andrew J Nelson, W James Nachury, Maxence V eLife Cell Biology The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of Somatostatin Receptor 3 (SSTR3, a GPCR) and Smoothened (Smo, a Hedgehog signal transducer) in the ciliary membrane. While IFT trains moved processively from one end of the cilium to the other, single SSTR3 and Smo underwent mostly diffusive behavior interspersed with short periods of directional movements. Statistical subtraction of instant velocities revealed that SSTR3 and Smo spent less than a third of their time undergoing active transport. Finally, SSTR3 and IFT movements could be uncoupled by perturbing either membrane protein diffusion or active transport. Thus ciliary membrane proteins move predominantly by diffusion, and attachment to IFT trains is transient and stochastic rather than processive or spatially determined. DOI: http://dx.doi.org/10.7554/eLife.00654.001 eLife Sciences Publications, Ltd 2013-08-06 /pmc/articles/PMC3736543/ /pubmed/23930224 http://dx.doi.org/10.7554/eLife.00654 Text en Copyright © 2013, Ye 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 | Cell Biology Ye, Fan Breslow, David K Koslover, Elena F Spakowitz, Andrew J Nelson, W James Nachury, Maxence V Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title | Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title_full | Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title_fullStr | Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title_full_unstemmed | Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title_short | Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
title_sort | single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736543/ https://www.ncbi.nlm.nih.gov/pubmed/23930224 http://dx.doi.org/10.7554/eLife.00654 |
work_keys_str_mv | AT yefan singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors AT breslowdavidk singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors AT kosloverelenaf singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors AT spakowitzandrewj singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors AT nelsonwjames singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors AT nachurymaxencev singlemoleculeimagingrevealsamajorrolefordiffusionintheexplorationofciliaryspacebysignalingreceptors |