Cargando…
Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds
A useful technique for culturing cells in a self-assembling nanofiber three-dimensional (3D) scaffold is described. This culture system recreates an environment that closely mimics the structural features of non-polarized tissue. Furthermore, the particular intrinsic nanofiber structure of the scaff...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101701/ https://www.ncbi.nlm.nih.gov/pubmed/29985312 http://dx.doi.org/10.3791/57259 |
_version_ | 1783349057456963584 |
---|---|
author | Betriu, Nausika Recha-Sancho, Lourdes Semino, Carlos E. |
author_facet | Betriu, Nausika Recha-Sancho, Lourdes Semino, Carlos E. |
author_sort | Betriu, Nausika |
collection | PubMed |
description | A useful technique for culturing cells in a self-assembling nanofiber three-dimensional (3D) scaffold is described. This culture system recreates an environment that closely mimics the structural features of non-polarized tissue. Furthermore, the particular intrinsic nanofiber structure of the scaffold makes it transparent to visual light, which allows for easy visualization of the sample under microscopy. This advantage was largely used to study cell migration, organization, proliferation, and differentiation and thus any development of their particular cellular function by staining with specific dyes or probes. Furthermore, in this work, we describe the good performance of this system to easily study the redifferentiation of expanded human articular chondrocytes into cartilaginous tissue. Cells were encapsulated into self-assembling peptide scaffolds and cultured under specific conditions to promote chondrogenesis. Three-dimensional cultures showed good viability during the 4 weeks of the experiment. As expected, samples cultured with chondrogenic inducers (compared to non-induced controls) stained strongly positive for toluidine blue (which stains glycosaminoglycans (GAGs) that are highly present in cartilage extracellular matrix) and expressed specific molecular markers, including collagen type I, II and X, according to Western Blot analysis. This protocol is easy to perform and can be used at research laboratories, industries and for educational purposes in laboratory courses. |
format | Online Article Text |
id | pubmed-6101701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-61017012018-09-11 Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds Betriu, Nausika Recha-Sancho, Lourdes Semino, Carlos E. J Vis Exp Bioengineering A useful technique for culturing cells in a self-assembling nanofiber three-dimensional (3D) scaffold is described. This culture system recreates an environment that closely mimics the structural features of non-polarized tissue. Furthermore, the particular intrinsic nanofiber structure of the scaffold makes it transparent to visual light, which allows for easy visualization of the sample under microscopy. This advantage was largely used to study cell migration, organization, proliferation, and differentiation and thus any development of their particular cellular function by staining with specific dyes or probes. Furthermore, in this work, we describe the good performance of this system to easily study the redifferentiation of expanded human articular chondrocytes into cartilaginous tissue. Cells were encapsulated into self-assembling peptide scaffolds and cultured under specific conditions to promote chondrogenesis. Three-dimensional cultures showed good viability during the 4 weeks of the experiment. As expected, samples cultured with chondrogenic inducers (compared to non-induced controls) stained strongly positive for toluidine blue (which stains glycosaminoglycans (GAGs) that are highly present in cartilage extracellular matrix) and expressed specific molecular markers, including collagen type I, II and X, according to Western Blot analysis. This protocol is easy to perform and can be used at research laboratories, industries and for educational purposes in laboratory courses. MyJove Corporation 2018-06-13 /pmc/articles/PMC6101701/ /pubmed/29985312 http://dx.doi.org/10.3791/57259 Text en Copyright © 2018, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Bioengineering Betriu, Nausika Recha-Sancho, Lourdes Semino, Carlos E. Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title | Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title_full | Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title_fullStr | Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title_full_unstemmed | Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title_short | Culturing Mammalian Cells in Three-dimensional Peptide Scaffolds |
title_sort | culturing mammalian cells in three-dimensional peptide scaffolds |
topic | Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101701/ https://www.ncbi.nlm.nih.gov/pubmed/29985312 http://dx.doi.org/10.3791/57259 |
work_keys_str_mv | AT betriunausika culturingmammaliancellsinthreedimensionalpeptidescaffolds AT rechasancholourdes culturingmammaliancellsinthreedimensionalpeptidescaffolds AT seminocarlose culturingmammaliancellsinthreedimensionalpeptidescaffolds |