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Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering

A one-step microfluidic system is developed in this study which enables the encapsulation of stem cells and genetically engineered non-pathogenic bacteria into a so-called three-dimensional (3D) pearl lace–like microgel of alginate with high level of monodispersity and cell viability. The alginate-b...

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Detalles Bibliográficos
Autores principales: Witte, K., Rodrigo-Navarro, A., Salmeron-Sanchez, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061548/
https://www.ncbi.nlm.nih.gov/pubmed/32159146
http://dx.doi.org/10.1016/j.mtbio.2019.100011
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author Witte, K.
Rodrigo-Navarro, A.
Salmeron-Sanchez, M.
author_facet Witte, K.
Rodrigo-Navarro, A.
Salmeron-Sanchez, M.
author_sort Witte, K.
collection PubMed
description A one-step microfluidic system is developed in this study which enables the encapsulation of stem cells and genetically engineered non-pathogenic bacteria into a so-called three-dimensional (3D) pearl lace–like microgel of alginate with high level of monodispersity and cell viability. The alginate-based microgel constitutes living materials that control stem cell differentiation in either an autonomous or heteronomous manner. The bacteria (Lactococcus lactis) encapsulated within the construct surface display adhesion fragments (III(7-10) fragment of human fibronectin) for integrin binding while secreting growth factors (recombinant human bone morphogenetic protein-2) to induce osteogenic differentiation of human bone marrow–derived mesenchymal stem cells. We concentrate on interlinked pearl lace microgels that enabled us to prototype a low-cost 3D bioprinting platform with highly tunable properties.
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spelling pubmed-70615482020-03-10 Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering Witte, K. Rodrigo-Navarro, A. Salmeron-Sanchez, M. Mater Today Bio Full-Length Article A one-step microfluidic system is developed in this study which enables the encapsulation of stem cells and genetically engineered non-pathogenic bacteria into a so-called three-dimensional (3D) pearl lace–like microgel of alginate with high level of monodispersity and cell viability. The alginate-based microgel constitutes living materials that control stem cell differentiation in either an autonomous or heteronomous manner. The bacteria (Lactococcus lactis) encapsulated within the construct surface display adhesion fragments (III(7-10) fragment of human fibronectin) for integrin binding while secreting growth factors (recombinant human bone morphogenetic protein-2) to induce osteogenic differentiation of human bone marrow–derived mesenchymal stem cells. We concentrate on interlinked pearl lace microgels that enabled us to prototype a low-cost 3D bioprinting platform with highly tunable properties. Elsevier 2019-06-18 /pmc/articles/PMC7061548/ /pubmed/32159146 http://dx.doi.org/10.1016/j.mtbio.2019.100011 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Full-Length Article
Witte, K.
Rodrigo-Navarro, A.
Salmeron-Sanchez, M.
Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title_full Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title_fullStr Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title_full_unstemmed Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title_short Bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
title_sort bacteria-laden microgels as autonomous three-dimensional environments for stem cell engineering
topic Full-Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061548/
https://www.ncbi.nlm.nih.gov/pubmed/32159146
http://dx.doi.org/10.1016/j.mtbio.2019.100011
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