The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy

The plasma membrane delimits the cell, which is the basic unit of living organisms, and is also a privileged site for cell communication with the environment. Cell adhesion can occur through cell-cell and cell-matrix contacts. Adhesion proteins such as integrins and cadherins also constitute recepto...

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Main Author: Arnauld eSergé
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-05-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00036/full
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spelling doaj-32a2f46087514d7da27c8ab9b219561c2020-11-25T00:46:29ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2016-05-01410.3389/fcell.2016.00036191695The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by VideonanoscopyArnauld eSergé0Aix-Marseille UniversityThe plasma membrane delimits the cell, which is the basic unit of living organisms, and is also a privileged site for cell communication with the environment. Cell adhesion can occur through cell-cell and cell-matrix contacts. Adhesion proteins such as integrins and cadherins also constitute receptors for inside-out and outside-in signaling within proteolipidic platforms. Adhesion molecule targeting and stabilization relies on specific features such as preferential segregation by the sub-membrane cytoskeleton meshwork and within membrane proteolipidic microdomains. This review presents an overview of the recent insights brought by the latest developments in microscopy, to unravel the molecular remodeling occurring at cell contacts. The dynamic aspect of cell adhesion was recently highlighted by super-resolution videomicroscopy, also named videonanoscopy. By circumventing the diffraction limit of light, nanoscopy has allowed the monitoring of molecular localization and behavior at the single-molecule level, on fixed and living cells. Accessing molecular-resolution details such as quantitatively monitoring components entering and leaving cell contacts by lateral diffusion and reversible association has revealed an unexpected plasticity. Adhesion structures can be highly specialized, such as focal adhesion in motile cells, as well as immune and neuronal synapses. Spatiotemporal reorganization of adhesion molecules, receptors and adaptors directly relates to structure/function modulation. Assembly of these supramolecular complexes is continuously balanced by dynamic events, remodeling adhesions on various timescales, notably by molecular conformation switches, lateral diffusion within the membrane and endo/exocytosis. Pathological alterations in cell adhesion are involved in cancer evolution, through cancer stem cell interaction with stromal niches, growth, extravasation and metastasis.http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00036/fullDiffusionsynapsemembrane dynamicsSingle moleculefocal adhesionsuper-resolution
collection DOAJ
language English
format Article
sources DOAJ
author Arnauld eSergé
spellingShingle Arnauld eSergé
The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
Frontiers in Cell and Developmental Biology
Diffusion
synapse
membrane dynamics
Single molecule
focal adhesion
super-resolution
author_facet Arnauld eSergé
author_sort Arnauld eSergé
title The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
title_short The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
title_full The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
title_fullStr The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
title_full_unstemmed The Molecular Architecture of Cell Adhesion: Dynamic Remodeling Revealed by Videonanoscopy
title_sort molecular architecture of cell adhesion: dynamic remodeling revealed by videonanoscopy
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2016-05-01
description The plasma membrane delimits the cell, which is the basic unit of living organisms, and is also a privileged site for cell communication with the environment. Cell adhesion can occur through cell-cell and cell-matrix contacts. Adhesion proteins such as integrins and cadherins also constitute receptors for inside-out and outside-in signaling within proteolipidic platforms. Adhesion molecule targeting and stabilization relies on specific features such as preferential segregation by the sub-membrane cytoskeleton meshwork and within membrane proteolipidic microdomains. This review presents an overview of the recent insights brought by the latest developments in microscopy, to unravel the molecular remodeling occurring at cell contacts. The dynamic aspect of cell adhesion was recently highlighted by super-resolution videomicroscopy, also named videonanoscopy. By circumventing the diffraction limit of light, nanoscopy has allowed the monitoring of molecular localization and behavior at the single-molecule level, on fixed and living cells. Accessing molecular-resolution details such as quantitatively monitoring components entering and leaving cell contacts by lateral diffusion and reversible association has revealed an unexpected plasticity. Adhesion structures can be highly specialized, such as focal adhesion in motile cells, as well as immune and neuronal synapses. Spatiotemporal reorganization of adhesion molecules, receptors and adaptors directly relates to structure/function modulation. Assembly of these supramolecular complexes is continuously balanced by dynamic events, remodeling adhesions on various timescales, notably by molecular conformation switches, lateral diffusion within the membrane and endo/exocytosis. Pathological alterations in cell adhesion are involved in cancer evolution, through cancer stem cell interaction with stromal niches, growth, extravasation and metastasis.
topic Diffusion
synapse
membrane dynamics
Single molecule
focal adhesion
super-resolution
url http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00036/full
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