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Physical Confinement Impacts Cellular Phenotypes within Living Materials
[Image: see text] Additive manufacturing allows three-dimensional printing of polymeric materials together with cells, creating living materials for applications in biomedical research and biotechnology. However, an understanding of the cellular phenotype within living materials is lacking, which is...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375193/ https://www.ncbi.nlm.nih.gov/pubmed/32715284 http://dx.doi.org/10.1021/acsabm.0c00335 |
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author | Priks, Hans Butelmann, Tobias Illarionov, Aleksandr Johnston, Trevor G. Fellin, Christopher Tamm, Tarmo Nelson, Alshakim Kumar, Rahul Lahtvee, Petri-Jaan |
author_facet | Priks, Hans Butelmann, Tobias Illarionov, Aleksandr Johnston, Trevor G. Fellin, Christopher Tamm, Tarmo Nelson, Alshakim Kumar, Rahul Lahtvee, Petri-Jaan |
author_sort | Priks, Hans |
collection | PubMed |
description | [Image: see text] Additive manufacturing allows three-dimensional printing of polymeric materials together with cells, creating living materials for applications in biomedical research and biotechnology. However, an understanding of the cellular phenotype within living materials is lacking, which is a key limitation for their wider application. Herein, we present an approach to characterize the cellular phenotype within living materials. We immobilized the budding yeast Saccharomyces cerevisiae in three different photo-cross-linkable triblock polymeric hydrogels containing F127-bis-urethane methacrylate, F127-dimethacrylate, or poly(alkyl glycidyl ether)-dimethacrylate. Using optical and scanning electron microscopy, we showed that hydrogels based on these polymers were stable under physiological conditions, but yeast colonies showed differences in the interaction within the living materials. We found that the physical confinement, imparted by compositional and structural properties of the hydrogels, impacted the cellular phenotype by reducing the size of cells in living materials compared with suspension cells. These properties also contributed to the differences in immobilization patterns, growth of colonies, and colony coatings. We observed that a composition-dependent degradation of polymers was likely possible by cells residing in the living materials. In conclusion, our investigation highlights the need for a holistic understanding of the cellular response within hydrogels to facilitate the synthesis of application-specific polymers and the design of advanced living materials in the future. |
format | Online Article Text |
id | pubmed-7375193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73751932020-07-23 Physical Confinement Impacts Cellular Phenotypes within Living Materials Priks, Hans Butelmann, Tobias Illarionov, Aleksandr Johnston, Trevor G. Fellin, Christopher Tamm, Tarmo Nelson, Alshakim Kumar, Rahul Lahtvee, Petri-Jaan ACS Appl Bio Mater [Image: see text] Additive manufacturing allows three-dimensional printing of polymeric materials together with cells, creating living materials for applications in biomedical research and biotechnology. However, an understanding of the cellular phenotype within living materials is lacking, which is a key limitation for their wider application. Herein, we present an approach to characterize the cellular phenotype within living materials. We immobilized the budding yeast Saccharomyces cerevisiae in three different photo-cross-linkable triblock polymeric hydrogels containing F127-bis-urethane methacrylate, F127-dimethacrylate, or poly(alkyl glycidyl ether)-dimethacrylate. Using optical and scanning electron microscopy, we showed that hydrogels based on these polymers were stable under physiological conditions, but yeast colonies showed differences in the interaction within the living materials. We found that the physical confinement, imparted by compositional and structural properties of the hydrogels, impacted the cellular phenotype by reducing the size of cells in living materials compared with suspension cells. These properties also contributed to the differences in immobilization patterns, growth of colonies, and colony coatings. We observed that a composition-dependent degradation of polymers was likely possible by cells residing in the living materials. In conclusion, our investigation highlights the need for a holistic understanding of the cellular response within hydrogels to facilitate the synthesis of application-specific polymers and the design of advanced living materials in the future. American Chemical Society 2020-06-07 2020-07-20 /pmc/articles/PMC7375193/ /pubmed/32715284 http://dx.doi.org/10.1021/acsabm.0c00335 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Priks, Hans Butelmann, Tobias Illarionov, Aleksandr Johnston, Trevor G. Fellin, Christopher Tamm, Tarmo Nelson, Alshakim Kumar, Rahul Lahtvee, Petri-Jaan Physical Confinement Impacts Cellular Phenotypes within Living Materials |
title | Physical Confinement Impacts Cellular Phenotypes within
Living Materials |
title_full | Physical Confinement Impacts Cellular Phenotypes within
Living Materials |
title_fullStr | Physical Confinement Impacts Cellular Phenotypes within
Living Materials |
title_full_unstemmed | Physical Confinement Impacts Cellular Phenotypes within
Living Materials |
title_short | Physical Confinement Impacts Cellular Phenotypes within
Living Materials |
title_sort | physical confinement impacts cellular phenotypes within
living materials |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375193/ https://www.ncbi.nlm.nih.gov/pubmed/32715284 http://dx.doi.org/10.1021/acsabm.0c00335 |
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