Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold

The use of filling biomaterials or tissue-engineered large bone implant-coupling biocompatible materials and human bone marrow mesenchymal stromal cells seems to be a promising approach to treat critical-sized bone defects. However, the cellular seeding onto and into large porous scaffolds still rem...

Full description

Bibliographic Details
Main Authors: S. Lemonnier, T. Bouderlique, S. Naili, H. Rouard, J. Courty, N. Chevallier, P. Albanese, T. Lemaire
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Applied Bionics and Biomechanics
Online Access:http://dx.doi.org/10.1155/2017/8949264
id doaj-b41c7423cdb64587a227146ed5a17913
record_format Article
spelling doaj-b41c7423cdb64587a227146ed5a179132021-07-02T01:05:24ZengHindawi LimitedApplied Bionics and Biomechanics1176-23221754-21032017-01-01201710.1155/2017/89492648949264Cell Colonization Ability of a Commercialized Large Porous Alveolar ScaffoldS. Lemonnier0T. Bouderlique1S. Naili2H. Rouard3J. Courty4N. Chevallier5P. Albanese6T. Lemaire7Laboratoire Modélisation et Simulation Multi Echelle-Biomécanique (MSME), UMR 8208 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceLaboratoire Croissance, Réparation et Régénération Tissulaires (CRRET), EA 4397, ERL 9215 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceLaboratoire Modélisation et Simulation Multi Echelle-Biomécanique (MSME), UMR 8208 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceLaboratoire Bioingénierie Cellulaire, Tissulaire et Sanguine à Visée Thérapeutique, EA EFS 3952, Université Paris-Est, 51 avenue du Maréchal de Lattre de Tassigny, 94010 Créteil, FranceLaboratoire Croissance, Réparation et Régénération Tissulaires (CRRET), EA 4397, ERL 9215 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceLaboratoire Bioingénierie Cellulaire, Tissulaire et Sanguine à Visée Thérapeutique, EA EFS 3952, Université Paris-Est, 51 avenue du Maréchal de Lattre de Tassigny, 94010 Créteil, FranceLaboratoire Croissance, Réparation et Régénération Tissulaires (CRRET), EA 4397, ERL 9215 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceLaboratoire Modélisation et Simulation Multi Echelle-Biomécanique (MSME), UMR 8208 CNRS, Université Paris-Est, 61 avenue du Général de Gaulle, 94010 Créteil, FranceThe use of filling biomaterials or tissue-engineered large bone implant-coupling biocompatible materials and human bone marrow mesenchymal stromal cells seems to be a promising approach to treat critical-sized bone defects. However, the cellular seeding onto and into large porous scaffolds still remains challenging since this process highly depends on the porous microstructure. Indeed, the cells may mainly colonize the periphery of the scaffold, leaving its volume almost free of cells. In this study, we carry out an in vitro study to analyze the ability of a commercialized scaffold to be in vivo colonized by cells. We investigate the influence of various physical parameters on the seeding efficiency of a perfusion seeding protocol using large manufactured bone substitutes. The present study shows that the velocity of the perfusion fluid and the initial cell density seem to impact the seeding results and to have a negative effect on the cellular viability, whereas the duration of the fluid perfusion and the nature of the flow (steady versus pulsed) did not show any influence on either the fraction of seeded cells or the cellular viability rate. However, the cellular repartition after seeding remains highly heterogeneous.http://dx.doi.org/10.1155/2017/8949264
collection DOAJ
language English
format Article
sources DOAJ
author S. Lemonnier
T. Bouderlique
S. Naili
H. Rouard
J. Courty
N. Chevallier
P. Albanese
T. Lemaire
spellingShingle S. Lemonnier
T. Bouderlique
S. Naili
H. Rouard
J. Courty
N. Chevallier
P. Albanese
T. Lemaire
Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
Applied Bionics and Biomechanics
author_facet S. Lemonnier
T. Bouderlique
S. Naili
H. Rouard
J. Courty
N. Chevallier
P. Albanese
T. Lemaire
author_sort S. Lemonnier
title Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
title_short Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
title_full Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
title_fullStr Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
title_full_unstemmed Cell Colonization Ability of a Commercialized Large Porous Alveolar Scaffold
title_sort cell colonization ability of a commercialized large porous alveolar scaffold
publisher Hindawi Limited
series Applied Bionics and Biomechanics
issn 1176-2322
1754-2103
publishDate 2017-01-01
description The use of filling biomaterials or tissue-engineered large bone implant-coupling biocompatible materials and human bone marrow mesenchymal stromal cells seems to be a promising approach to treat critical-sized bone defects. However, the cellular seeding onto and into large porous scaffolds still remains challenging since this process highly depends on the porous microstructure. Indeed, the cells may mainly colonize the periphery of the scaffold, leaving its volume almost free of cells. In this study, we carry out an in vitro study to analyze the ability of a commercialized scaffold to be in vivo colonized by cells. We investigate the influence of various physical parameters on the seeding efficiency of a perfusion seeding protocol using large manufactured bone substitutes. The present study shows that the velocity of the perfusion fluid and the initial cell density seem to impact the seeding results and to have a negative effect on the cellular viability, whereas the duration of the fluid perfusion and the nature of the flow (steady versus pulsed) did not show any influence on either the fraction of seeded cells or the cellular viability rate. However, the cellular repartition after seeding remains highly heterogeneous.
url http://dx.doi.org/10.1155/2017/8949264
work_keys_str_mv AT slemonnier cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT tbouderlique cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT snaili cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT hrouard cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT jcourty cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT nchevallier cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT palbanese cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
AT tlemaire cellcolonizationabilityofacommercializedlargeporousalveolarscaffold
_version_ 1721345588155383808