Cargando…

A step toward engineering thick tissues: Distributing microfibers within 3D printed frames

Microfiber mats for tissue engineering scaffolds support cell growth, but are limited by poor cell infiltration and nutrient transport. Three‐dimensional printing, specifically fused deposition modeling (FDM), can rapidly produce customized constructs, but macroscopic porosity resulting from low res...

Descripción completa

Detalles Bibliográficos
Autores principales: Molde, Joseph, Steele, Joseph A. M., Pastino, Alexandra K., Mahat, Anisha, Murthy, N. Sanjeeva, Kohn, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078963/
https://www.ncbi.nlm.nih.gov/pubmed/31721423
http://dx.doi.org/10.1002/jbm.a.36838
_version_ 1783507728350576640
author Molde, Joseph
Steele, Joseph A. M.
Pastino, Alexandra K.
Mahat, Anisha
Murthy, N. Sanjeeva
Kohn, Joachim
author_facet Molde, Joseph
Steele, Joseph A. M.
Pastino, Alexandra K.
Mahat, Anisha
Murthy, N. Sanjeeva
Kohn, Joachim
author_sort Molde, Joseph
collection PubMed
description Microfiber mats for tissue engineering scaffolds support cell growth, but are limited by poor cell infiltration and nutrient transport. Three‐dimensional printing, specifically fused deposition modeling (FDM), can rapidly produce customized constructs, but macroscopic porosity resulting from low resolution reduces cell seeding efficiency and prevents the formation of continuous cell networks. Here we describe the fabrication of hierarchical scaffolds that integrate a fibrous microenvironment with the open macropore structure of FDM. Biodegradable tyrosine‐derived polycarbonate microfibers were airbrushed iteratively between layers of 3D printed support structure following optimization. Confocal imaging showed layers of airbrushed fiber mats supported human dermal fibroblast growth and extracellular matrix development throughout the scaffold. When implanted subcutaneously, hierarchical scaffolds facilitated greater cell infiltration and tissue formation than airbrushed fiber mats. Fibronectin matrix assembled in vitro throughout the hierarchical scaffold survived decellularization and provided a hybrid substrate for recellularization with mesenchymal stromal cells. These results demonstrate that by combining FDM and airbrushing techniques we can engineer customizable hierarchical scaffolds for thick tissues that support increased cell growth and infiltration.
format Online
Article
Text
id pubmed-7078963
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-70789632020-03-19 A step toward engineering thick tissues: Distributing microfibers within 3D printed frames Molde, Joseph Steele, Joseph A. M. Pastino, Alexandra K. Mahat, Anisha Murthy, N. Sanjeeva Kohn, Joachim J Biomed Mater Res A Original Articles Microfiber mats for tissue engineering scaffolds support cell growth, but are limited by poor cell infiltration and nutrient transport. Three‐dimensional printing, specifically fused deposition modeling (FDM), can rapidly produce customized constructs, but macroscopic porosity resulting from low resolution reduces cell seeding efficiency and prevents the formation of continuous cell networks. Here we describe the fabrication of hierarchical scaffolds that integrate a fibrous microenvironment with the open macropore structure of FDM. Biodegradable tyrosine‐derived polycarbonate microfibers were airbrushed iteratively between layers of 3D printed support structure following optimization. Confocal imaging showed layers of airbrushed fiber mats supported human dermal fibroblast growth and extracellular matrix development throughout the scaffold. When implanted subcutaneously, hierarchical scaffolds facilitated greater cell infiltration and tissue formation than airbrushed fiber mats. Fibronectin matrix assembled in vitro throughout the hierarchical scaffold survived decellularization and provided a hybrid substrate for recellularization with mesenchymal stromal cells. These results demonstrate that by combining FDM and airbrushing techniques we can engineer customizable hierarchical scaffolds for thick tissues that support increased cell growth and infiltration. John Wiley & Sons, Inc. 2019-12-24 2020-03 /pmc/articles/PMC7078963/ /pubmed/31721423 http://dx.doi.org/10.1002/jbm.a.36838 Text en © 2019 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Molde, Joseph
Steele, Joseph A. M.
Pastino, Alexandra K.
Mahat, Anisha
Murthy, N. Sanjeeva
Kohn, Joachim
A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title_full A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title_fullStr A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title_full_unstemmed A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title_short A step toward engineering thick tissues: Distributing microfibers within 3D printed frames
title_sort step toward engineering thick tissues: distributing microfibers within 3d printed frames
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078963/
https://www.ncbi.nlm.nih.gov/pubmed/31721423
http://dx.doi.org/10.1002/jbm.a.36838
work_keys_str_mv AT moldejoseph asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT steelejosepham asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT pastinoalexandrak asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT mahatanisha asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT murthynsanjeeva asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT kohnjoachim asteptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT moldejoseph steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT steelejosepham steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT pastinoalexandrak steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT mahatanisha steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT murthynsanjeeva steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes
AT kohnjoachim steptowardengineeringthicktissuesdistributingmicrofiberswithin3dprintedframes