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Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization

Traditional two-dimensional (2D) cell culture models are limited in their ability to reproduce human structures and functions. On the contrary, three-dimensional (3D) microtissues have the potential to permit the development of new cell-based assays as advanced in vitro models to test new drugs. Her...

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Autores principales: Pitingolo, Gabriele, Riaud, Antoine, Nastruzzi, Claudio, Taly, Valerie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523541/
https://www.ncbi.nlm.nih.gov/pubmed/31010232
http://dx.doi.org/10.3390/mi10040265
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author Pitingolo, Gabriele
Riaud, Antoine
Nastruzzi, Claudio
Taly, Valerie
author_facet Pitingolo, Gabriele
Riaud, Antoine
Nastruzzi, Claudio
Taly, Valerie
author_sort Pitingolo, Gabriele
collection PubMed
description Traditional two-dimensional (2D) cell culture models are limited in their ability to reproduce human structures and functions. On the contrary, three-dimensional (3D) microtissues have the potential to permit the development of new cell-based assays as advanced in vitro models to test new drugs. Here, we report the use of a dehydrated gelatin film to promote tumor cells aggregation and 3D microtissue formation. The simple and stable gelatin coating represents an alternative to conventional and expensive materials like type I collagen, hyaluronic acid, or matrigel. The gelatin coating is biocompatible with several culture formats including microfluidic chips, as well as standard micro-well plates. It also enables long-term 3D cell culture and in situ monitoring of live/dead assays.
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spelling pubmed-65235412019-06-03 Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization Pitingolo, Gabriele Riaud, Antoine Nastruzzi, Claudio Taly, Valerie Micromachines (Basel) Communication Traditional two-dimensional (2D) cell culture models are limited in their ability to reproduce human structures and functions. On the contrary, three-dimensional (3D) microtissues have the potential to permit the development of new cell-based assays as advanced in vitro models to test new drugs. Here, we report the use of a dehydrated gelatin film to promote tumor cells aggregation and 3D microtissue formation. The simple and stable gelatin coating represents an alternative to conventional and expensive materials like type I collagen, hyaluronic acid, or matrigel. The gelatin coating is biocompatible with several culture formats including microfluidic chips, as well as standard micro-well plates. It also enables long-term 3D cell culture and in situ monitoring of live/dead assays. MDPI 2019-04-19 /pmc/articles/PMC6523541/ /pubmed/31010232 http://dx.doi.org/10.3390/mi10040265 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Pitingolo, Gabriele
Riaud, Antoine
Nastruzzi, Claudio
Taly, Valerie
Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title_full Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title_fullStr Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title_full_unstemmed Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title_short Gelatin-Coated Microfluidic Channels for 3D Microtissue Formation: On-Chip Production and Characterization
title_sort gelatin-coated microfluidic channels for 3d microtissue formation: on-chip production and characterization
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523541/
https://www.ncbi.nlm.nih.gov/pubmed/31010232
http://dx.doi.org/10.3390/mi10040265
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