Cargando…

The tetraspanin web revisited by super-resolution microscopy

The spatial organization of membrane proteins in the plasma membrane is critical for signal transduction, cell communication and membrane trafficking. Tetraspanins organize functional higher-order protein complexes called ‘tetraspanin-enriched microdomains (TEMs)’ via interactions with partner molec...

Descripción completa

Detalles Bibliográficos
Autores principales: Zuidscherwoude, Malou, Göttfert, Fabian, Dunlock, Vera Marie E., Figdor, Carl G., van den Bogaart, Geert, Spriel, Annemiek B. van
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505338/
https://www.ncbi.nlm.nih.gov/pubmed/26183063
http://dx.doi.org/10.1038/srep12201
_version_ 1782381570374500352
author Zuidscherwoude, Malou
Göttfert, Fabian
Dunlock, Vera Marie E.
Figdor, Carl G.
van den Bogaart, Geert
Spriel, Annemiek B. van
author_facet Zuidscherwoude, Malou
Göttfert, Fabian
Dunlock, Vera Marie E.
Figdor, Carl G.
van den Bogaart, Geert
Spriel, Annemiek B. van
author_sort Zuidscherwoude, Malou
collection PubMed
description The spatial organization of membrane proteins in the plasma membrane is critical for signal transduction, cell communication and membrane trafficking. Tetraspanins organize functional higher-order protein complexes called ‘tetraspanin-enriched microdomains (TEMs)’ via interactions with partner molecules and other tetraspanins. Still, the nanoscale organization of TEMs in native plasma membranes has not been resolved. Here, we elucidated the size, density and distribution of TEMs in the plasma membrane of human B cells and dendritic cells using dual color stimulated emission depletion (STED) microscopy. We demonstrate that tetraspanins form individual nanoclusters smaller than 120 nm and quantified that a single tetraspanin CD53 cluster contains less than ten CD53 molecules. CD53 and CD37 domains were adjacent to and displayed only minor overlap with clusters containing tetraspanins CD81 or CD82. Moreover, CD53 and CD81 were found in closer proximity to their partners MHC class II and CD19 than to other tetraspanins. Although these results indicate that tetraspanin domains are adjacently positioned in the plasma membrane, they challenge the current view of the tetraspanin web of multiple tetraspanin species organized into a single domain. This study increases the molecular understanding of TEMs at the nanoscale level which is essential for comprehending tetraspanin function in cell biology.
format Online
Article
Text
id pubmed-4505338
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-45053382015-07-23 The tetraspanin web revisited by super-resolution microscopy Zuidscherwoude, Malou Göttfert, Fabian Dunlock, Vera Marie E. Figdor, Carl G. van den Bogaart, Geert Spriel, Annemiek B. van Sci Rep Article The spatial organization of membrane proteins in the plasma membrane is critical for signal transduction, cell communication and membrane trafficking. Tetraspanins organize functional higher-order protein complexes called ‘tetraspanin-enriched microdomains (TEMs)’ via interactions with partner molecules and other tetraspanins. Still, the nanoscale organization of TEMs in native plasma membranes has not been resolved. Here, we elucidated the size, density and distribution of TEMs in the plasma membrane of human B cells and dendritic cells using dual color stimulated emission depletion (STED) microscopy. We demonstrate that tetraspanins form individual nanoclusters smaller than 120 nm and quantified that a single tetraspanin CD53 cluster contains less than ten CD53 molecules. CD53 and CD37 domains were adjacent to and displayed only minor overlap with clusters containing tetraspanins CD81 or CD82. Moreover, CD53 and CD81 were found in closer proximity to their partners MHC class II and CD19 than to other tetraspanins. Although these results indicate that tetraspanin domains are adjacently positioned in the plasma membrane, they challenge the current view of the tetraspanin web of multiple tetraspanin species organized into a single domain. This study increases the molecular understanding of TEMs at the nanoscale level which is essential for comprehending tetraspanin function in cell biology. Nature Publishing Group 2015-07-17 /pmc/articles/PMC4505338/ /pubmed/26183063 http://dx.doi.org/10.1038/srep12201 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zuidscherwoude, Malou
Göttfert, Fabian
Dunlock, Vera Marie E.
Figdor, Carl G.
van den Bogaart, Geert
Spriel, Annemiek B. van
The tetraspanin web revisited by super-resolution microscopy
title The tetraspanin web revisited by super-resolution microscopy
title_full The tetraspanin web revisited by super-resolution microscopy
title_fullStr The tetraspanin web revisited by super-resolution microscopy
title_full_unstemmed The tetraspanin web revisited by super-resolution microscopy
title_short The tetraspanin web revisited by super-resolution microscopy
title_sort tetraspanin web revisited by super-resolution microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505338/
https://www.ncbi.nlm.nih.gov/pubmed/26183063
http://dx.doi.org/10.1038/srep12201
work_keys_str_mv AT zuidscherwoudemalou thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT gottfertfabian thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT dunlockveramariee thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT figdorcarlg thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT vandenbogaartgeert thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT sprielannemiekbvan thetetraspaninwebrevisitedbysuperresolutionmicroscopy
AT zuidscherwoudemalou tetraspaninwebrevisitedbysuperresolutionmicroscopy
AT gottfertfabian tetraspaninwebrevisitedbysuperresolutionmicroscopy
AT dunlockveramariee tetraspaninwebrevisitedbysuperresolutionmicroscopy
AT figdorcarlg tetraspaninwebrevisitedbysuperresolutionmicroscopy
AT vandenbogaartgeert tetraspaninwebrevisitedbysuperresolutionmicroscopy
AT sprielannemiekbvan tetraspaninwebrevisitedbysuperresolutionmicroscopy