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Mechanically Biomimetic Gelatin–Gellan Gum Hydrogels for 3D Culture of Beating Human Cardiomyocytes
[Image: see text] To promote the transition of cell cultures from 2D to 3D, hydrogels are needed to biomimic the extracellular matrix (ECM). One potential material for this purpose is gellan gum (GG), a biocompatible and mechanically tunable hydrogel. However, GG alone does not provide attachment si...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6750838/ https://www.ncbi.nlm.nih.gov/pubmed/31120238 http://dx.doi.org/10.1021/acsami.8b22343 |
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author | Koivisto, Janne T. Gering, Christine Karvinen, Jennika Maria Cherian, Reeja Belay, Birhanu Hyttinen, Jari Aalto-Setälä, Katriina Kellomäki, Minna Parraga, Jenny |
author_facet | Koivisto, Janne T. Gering, Christine Karvinen, Jennika Maria Cherian, Reeja Belay, Birhanu Hyttinen, Jari Aalto-Setälä, Katriina Kellomäki, Minna Parraga, Jenny |
author_sort | Koivisto, Janne T. |
collection | PubMed |
description | [Image: see text] To promote the transition of cell cultures from 2D to 3D, hydrogels are needed to biomimic the extracellular matrix (ECM). One potential material for this purpose is gellan gum (GG), a biocompatible and mechanically tunable hydrogel. However, GG alone does not provide attachment sites for cells to thrive in 3D. One option for biofunctionalization is the introduction of gelatin, a derivative of the abundant ECM protein collagen. Unfortunately, gelatin lacks cross-linking moieties, making the production of self-standing hydrogels difficult under physiological conditions. Here, we explore the functionalization of GG with gelatin at biologically relevant concentrations using semiorthogonal, cytocompatible, and facile chemistry based on hydrazone reaction. These hydrogels exhibit mechanical behavior, especially elasticity, which resembles the cardiac tissue. The use of optical projection tomography for 3D cell microscopy demonstrates good cytocompatibility and elongation of human fibroblasts (WI-38). In addition, human-induced pluripotent stem cell-derived cardiomyocytes attach to the hydrogels and recover their spontaneous beating in 24 h culture. Beating is studied using in-house-built phase contrast video analysis software, and it is comparable with the beating of control cardiomyocytes under regular culture conditions. These hydrogels provide a promising platform to transition cardiac tissue engineering and disease modeling from 2D to 3D. |
format | Online Article Text |
id | pubmed-6750838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67508382019-09-19 Mechanically Biomimetic Gelatin–Gellan Gum Hydrogels for 3D Culture of Beating Human Cardiomyocytes Koivisto, Janne T. Gering, Christine Karvinen, Jennika Maria Cherian, Reeja Belay, Birhanu Hyttinen, Jari Aalto-Setälä, Katriina Kellomäki, Minna Parraga, Jenny ACS Appl Mater Interfaces [Image: see text] To promote the transition of cell cultures from 2D to 3D, hydrogels are needed to biomimic the extracellular matrix (ECM). One potential material for this purpose is gellan gum (GG), a biocompatible and mechanically tunable hydrogel. However, GG alone does not provide attachment sites for cells to thrive in 3D. One option for biofunctionalization is the introduction of gelatin, a derivative of the abundant ECM protein collagen. Unfortunately, gelatin lacks cross-linking moieties, making the production of self-standing hydrogels difficult under physiological conditions. Here, we explore the functionalization of GG with gelatin at biologically relevant concentrations using semiorthogonal, cytocompatible, and facile chemistry based on hydrazone reaction. These hydrogels exhibit mechanical behavior, especially elasticity, which resembles the cardiac tissue. The use of optical projection tomography for 3D cell microscopy demonstrates good cytocompatibility and elongation of human fibroblasts (WI-38). In addition, human-induced pluripotent stem cell-derived cardiomyocytes attach to the hydrogels and recover their spontaneous beating in 24 h culture. Beating is studied using in-house-built phase contrast video analysis software, and it is comparable with the beating of control cardiomyocytes under regular culture conditions. These hydrogels provide a promising platform to transition cardiac tissue engineering and disease modeling from 2D to 3D. American Chemical Society 2019-05-23 2019-06-12 /pmc/articles/PMC6750838/ /pubmed/31120238 http://dx.doi.org/10.1021/acsami.8b22343 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Koivisto, Janne T. Gering, Christine Karvinen, Jennika Maria Cherian, Reeja Belay, Birhanu Hyttinen, Jari Aalto-Setälä, Katriina Kellomäki, Minna Parraga, Jenny Mechanically Biomimetic Gelatin–Gellan Gum Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title | Mechanically
Biomimetic Gelatin–Gellan Gum
Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title_full | Mechanically
Biomimetic Gelatin–Gellan Gum
Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title_fullStr | Mechanically
Biomimetic Gelatin–Gellan Gum
Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title_full_unstemmed | Mechanically
Biomimetic Gelatin–Gellan Gum
Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title_short | Mechanically
Biomimetic Gelatin–Gellan Gum
Hydrogels for 3D Culture of Beating Human Cardiomyocytes |
title_sort | mechanically
biomimetic gelatin–gellan gum
hydrogels for 3d culture of beating human cardiomyocytes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6750838/ https://www.ncbi.nlm.nih.gov/pubmed/31120238 http://dx.doi.org/10.1021/acsami.8b22343 |
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