Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.

Cellular density is a parameter measured for glioma grade and invasiveness diagnosis. The characterization of the cellular density can be performed, non invasively, by magnetic resonance imaging (MRI), since, this technique displays a good resolution. Nevertheless MRI sensitivity is critical. Develo...

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Main Authors: Damien Moncelet, Véronique Bouchaud, Philippe Mellet, Emeline Ribot, Sylvain Miraux, Jean-Michel Franconi, Pierre Voisin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3873929?pdf=render
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spelling doaj-a995bc88970b498fab72a144478f15542020-11-25T01:45:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8277710.1371/journal.pone.0082777Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.Damien MonceletVéronique BouchaudPhilippe MelletEmeline RibotSylvain MirauxJean-Michel FranconiPierre VoisinCellular density is a parameter measured for glioma grade and invasiveness diagnosis. The characterization of the cellular density can be performed, non invasively, by magnetic resonance imaging (MRI), since, this technique displays a good resolution. Nevertheless MRI sensitivity is critical. Development of smart contrast agents appears useful to increase MRI signal to noise ratio (SNR). Tumor invasiveness is correlated with high expression of integrins that can be targeted by RGD motif. In this study, MRI contrast agents or fluorescent probes linked to RGD-peptides were used, in a glioma model, to assess the relation between RGD uptake/signal improvement/cell density and consequently tumor invasiveness. Experiments were performed in vitro with U87-MG glioma cells. Flow cytometry and microscopy experiments with RGD and iRGD-alexa488 demonstrated that cell internalization was dependent on cell density. The internalization involved a clathrin-dependent endocytosis. Cytoskeleton and particularly the microtubules were concerned. Actin filaments played a minor role. The internalization was also dependent on the glycolysis and the oxidative phosphorylations. The cellular density modulated the importance of the endocytosis pathways and of the metabolism but not the cytoskeleton contribution. The internalization of the RGD-peptide associated to gadolinium chelate increased the SNR of U87 cells. Moreover, following the cell density augmentation, the SNR increased with a low amplitude but a trend was clearly determined. In conclusion, RGD-peptide internalization appeared, in vitro, as a marker of cellular density. In perspective, the combination of these peptides with contrast agents associated to more sensitive MRI techniques could improve the MRI signal allowing the characterization of cellular density for tumor diagnosis.http://europepmc.org/articles/PMC3873929?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Damien Moncelet
Véronique Bouchaud
Philippe Mellet
Emeline Ribot
Sylvain Miraux
Jean-Michel Franconi
Pierre Voisin
spellingShingle Damien Moncelet
Véronique Bouchaud
Philippe Mellet
Emeline Ribot
Sylvain Miraux
Jean-Michel Franconi
Pierre Voisin
Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
PLoS ONE
author_facet Damien Moncelet
Véronique Bouchaud
Philippe Mellet
Emeline Ribot
Sylvain Miraux
Jean-Michel Franconi
Pierre Voisin
author_sort Damien Moncelet
title Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
title_short Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
title_full Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
title_fullStr Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
title_full_unstemmed Cellular density effect on RGD ligand internalization in glioblastoma for MRI application.
title_sort cellular density effect on rgd ligand internalization in glioblastoma for mri application.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Cellular density is a parameter measured for glioma grade and invasiveness diagnosis. The characterization of the cellular density can be performed, non invasively, by magnetic resonance imaging (MRI), since, this technique displays a good resolution. Nevertheless MRI sensitivity is critical. Development of smart contrast agents appears useful to increase MRI signal to noise ratio (SNR). Tumor invasiveness is correlated with high expression of integrins that can be targeted by RGD motif. In this study, MRI contrast agents or fluorescent probes linked to RGD-peptides were used, in a glioma model, to assess the relation between RGD uptake/signal improvement/cell density and consequently tumor invasiveness. Experiments were performed in vitro with U87-MG glioma cells. Flow cytometry and microscopy experiments with RGD and iRGD-alexa488 demonstrated that cell internalization was dependent on cell density. The internalization involved a clathrin-dependent endocytosis. Cytoskeleton and particularly the microtubules were concerned. Actin filaments played a minor role. The internalization was also dependent on the glycolysis and the oxidative phosphorylations. The cellular density modulated the importance of the endocytosis pathways and of the metabolism but not the cytoskeleton contribution. The internalization of the RGD-peptide associated to gadolinium chelate increased the SNR of U87 cells. Moreover, following the cell density augmentation, the SNR increased with a low amplitude but a trend was clearly determined. In conclusion, RGD-peptide internalization appeared, in vitro, as a marker of cellular density. In perspective, the combination of these peptides with contrast agents associated to more sensitive MRI techniques could improve the MRI signal allowing the characterization of cellular density for tumor diagnosis.
url http://europepmc.org/articles/PMC3873929?pdf=render
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