A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks

Excitatory glutamatergic synapses at dendritic spines exchange and modulate their receptor content via lateral membrane diffusion. Several studies have shown that the thin spine neck impedes the access of membrane and solute molecules to the spine head. However, it is unclear whether the spine neck...

Full description

Bibliographic Details
Main Authors: Ewers, Helge, Tada, Tomoko, Petersen, Jennifer D., Racz, Bence, Sheng, Morgan, Choquet, Daniel
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Language:en_US
Published: Public Library of Science 2014
Online Access:http://hdl.handle.net/1721.1/92480
_version_ 1826211290557710336
author Ewers, Helge
Tada, Tomoko
Petersen, Jennifer D.
Racz, Bence
Sheng, Morgan
Choquet, Daniel
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Ewers, Helge
Tada, Tomoko
Petersen, Jennifer D.
Racz, Bence
Sheng, Morgan
Choquet, Daniel
author_sort Ewers, Helge
collection MIT
description Excitatory glutamatergic synapses at dendritic spines exchange and modulate their receptor content via lateral membrane diffusion. Several studies have shown that the thin spine neck impedes the access of membrane and solute molecules to the spine head. However, it is unclear whether the spine neck geometry alone restricts access to dendritic spines or if a physical barrier to the diffusion of molecules exists. Here, we investigated whether a complex of septin cytoskeletal GTPases localized at the base of the spine neck regulates diffusion across the spine neck. We found that, during development, a marker of the septin complex, Septin7 (Sept7), becomes localized to the spine neck where it forms a stable structure underneath the plasma membrane. We show that diffusion of receptors and bulk membrane, but not cytoplasmic proteins, is slower in spines bearing Sept7 at their neck. Finally, when Sept7 expression was suppressed by RNA interference, membrane molecules explored larger membrane areas. Our findings indicate that Sept7 regulates membrane protein access to spines.
first_indexed 2024-09-23T15:03:35Z
format Article
id mit-1721.1/92480
institution Massachusetts Institute of Technology
language en_US
last_indexed 2024-09-23T15:03:35Z
publishDate 2014
publisher Public Library of Science
record_format dspace
spelling mit-1721.1/924802022-09-29T12:20:57Z A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks Ewers, Helge Tada, Tomoko Petersen, Jennifer D. Racz, Bence Sheng, Morgan Choquet, Daniel Massachusetts Institute of Technology. Department of Biology Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences Picower Institute for Learning and Memory Tada, Tomoko Excitatory glutamatergic synapses at dendritic spines exchange and modulate their receptor content via lateral membrane diffusion. Several studies have shown that the thin spine neck impedes the access of membrane and solute molecules to the spine head. However, it is unclear whether the spine neck geometry alone restricts access to dendritic spines or if a physical barrier to the diffusion of molecules exists. Here, we investigated whether a complex of septin cytoskeletal GTPases localized at the base of the spine neck regulates diffusion across the spine neck. We found that, during development, a marker of the septin complex, Septin7 (Sept7), becomes localized to the spine neck where it forms a stable structure underneath the plasma membrane. We show that diffusion of receptors and bulk membrane, but not cytoplasmic proteins, is slower in spines bearing Sept7 at their neck. Finally, when Sept7 expression was suppressed by RNA interference, membrane molecules explored larger membrane areas. Our findings indicate that Sept7 regulates membrane protein access to spines. Human Frontier Science Program (Strasbourg, France) (Short-Term Fellowship) 2014-12-23T19:52:29Z 2014-12-23T19:52:29Z 2014-12 2014-04 Article http://purl.org/eprint/type/JournalArticle 1932-6203 http://hdl.handle.net/1721.1/92480 Ewers, Helge, Tomoko Tada, Jennifer D. Petersen, Bence Racz, Morgan Sheng, and Daniel Choquet. “A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks.” Edited by Lin Mei. PLoS ONE 9, no. 12 (December 10, 2014): e113916. en_US http://dx.doi.org/10.1371/journal.pone.0113916 PLoS ONE Creative Commons Attribution http://creativecommons.org/licenses/by/4.0/ application/pdf Public Library of Science Public Library of Science
spellingShingle Ewers, Helge
Tada, Tomoko
Petersen, Jennifer D.
Racz, Bence
Sheng, Morgan
Choquet, Daniel
A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title_full A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title_fullStr A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title_full_unstemmed A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title_short A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks
title_sort septin dependent diffusion barrier at dendritic spine necks
url http://hdl.handle.net/1721.1/92480
work_keys_str_mv AT ewershelge aseptindependentdiffusionbarrieratdendriticspinenecks
AT tadatomoko aseptindependentdiffusionbarrieratdendriticspinenecks
AT petersenjenniferd aseptindependentdiffusionbarrieratdendriticspinenecks
AT raczbence aseptindependentdiffusionbarrieratdendriticspinenecks
AT shengmorgan aseptindependentdiffusionbarrieratdendriticspinenecks
AT choquetdaniel aseptindependentdiffusionbarrieratdendriticspinenecks
AT ewershelge septindependentdiffusionbarrieratdendriticspinenecks
AT tadatomoko septindependentdiffusionbarrieratdendriticspinenecks
AT petersenjenniferd septindependentdiffusionbarrieratdendriticspinenecks
AT raczbence septindependentdiffusionbarrieratdendriticspinenecks
AT shengmorgan septindependentdiffusionbarrieratdendriticspinenecks
AT choquetdaniel septindependentdiffusionbarrieratdendriticspinenecks