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Non-Invasive Three-Dimensional Cell Analysis in Bioinks by Raman Imaging
[Image: see text] 3D bioprinting is an emerging biofabrication strategy using bioinks, comprising cells and biocompatible materials, to produce functional tissue models. Despite progress in building increasingly complex objects, biological analyses in printed constructs remain challenging. Especiall...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284518/ https://www.ncbi.nlm.nih.gov/pubmed/35777738 http://dx.doi.org/10.1021/acsami.1c24463 |
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author | Marzi, Julia Fuhrmann, Ellena Brauchle, Eva Singer, Verena Pfannstiel, Jessica Schmidt, Isabelle Hartmann, Hanna |
author_facet | Marzi, Julia Fuhrmann, Ellena Brauchle, Eva Singer, Verena Pfannstiel, Jessica Schmidt, Isabelle Hartmann, Hanna |
author_sort | Marzi, Julia |
collection | PubMed |
description | [Image: see text] 3D bioprinting is an emerging biofabrication strategy using bioinks, comprising cells and biocompatible materials, to produce functional tissue models. Despite progress in building increasingly complex objects, biological analyses in printed constructs remain challenging. Especially, methods that allow non-invasive and non-destructive evaluation of embedded cells are largely missing. Here, we implemented Raman imaging for molecular-sensitive investigations on bioprinted objects. Different aspects such as culture formats (2D, 3D-cast, and 3D-printed), cell types (endothelial cells and fibroblasts), and the selection of the biopolymer (alginate, alginate/nanofibrillated cellulose, alginate/gelatin) were considered and evaluated. Raman imaging allowed for marker-independent identification and localization of subcellular components against the surrounding biomaterial background. Furthermore, single-cell analysis of spectral signatures, performed by multivariate analysis, demonstrated discrimination between endothelial cells and fibroblasts and identified cellular features influenced by the bioprinting process. In summary, Raman imaging was successfully established to analyze cells in 3D culture in situ and evaluate them with regard to the localization of different cell types and their molecular phenotype as a valuable tool for quality control of bioprinted objects. |
format | Online Article Text |
id | pubmed-9284518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92845182022-07-16 Non-Invasive Three-Dimensional Cell Analysis in Bioinks by Raman Imaging Marzi, Julia Fuhrmann, Ellena Brauchle, Eva Singer, Verena Pfannstiel, Jessica Schmidt, Isabelle Hartmann, Hanna ACS Appl Mater Interfaces [Image: see text] 3D bioprinting is an emerging biofabrication strategy using bioinks, comprising cells and biocompatible materials, to produce functional tissue models. Despite progress in building increasingly complex objects, biological analyses in printed constructs remain challenging. Especially, methods that allow non-invasive and non-destructive evaluation of embedded cells are largely missing. Here, we implemented Raman imaging for molecular-sensitive investigations on bioprinted objects. Different aspects such as culture formats (2D, 3D-cast, and 3D-printed), cell types (endothelial cells and fibroblasts), and the selection of the biopolymer (alginate, alginate/nanofibrillated cellulose, alginate/gelatin) were considered and evaluated. Raman imaging allowed for marker-independent identification and localization of subcellular components against the surrounding biomaterial background. Furthermore, single-cell analysis of spectral signatures, performed by multivariate analysis, demonstrated discrimination between endothelial cells and fibroblasts and identified cellular features influenced by the bioprinting process. In summary, Raman imaging was successfully established to analyze cells in 3D culture in situ and evaluate them with regard to the localization of different cell types and their molecular phenotype as a valuable tool for quality control of bioprinted objects. American Chemical Society 2022-07-01 2022-07-13 /pmc/articles/PMC9284518/ /pubmed/35777738 http://dx.doi.org/10.1021/acsami.1c24463 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Marzi, Julia Fuhrmann, Ellena Brauchle, Eva Singer, Verena Pfannstiel, Jessica Schmidt, Isabelle Hartmann, Hanna Non-Invasive Three-Dimensional Cell Analysis in Bioinks by Raman Imaging |
title | Non-Invasive
Three-Dimensional Cell Analysis in Bioinks
by Raman Imaging |
title_full | Non-Invasive
Three-Dimensional Cell Analysis in Bioinks
by Raman Imaging |
title_fullStr | Non-Invasive
Three-Dimensional Cell Analysis in Bioinks
by Raman Imaging |
title_full_unstemmed | Non-Invasive
Three-Dimensional Cell Analysis in Bioinks
by Raman Imaging |
title_short | Non-Invasive
Three-Dimensional Cell Analysis in Bioinks
by Raman Imaging |
title_sort | non-invasive
three-dimensional cell analysis in bioinks
by raman imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284518/ https://www.ncbi.nlm.nih.gov/pubmed/35777738 http://dx.doi.org/10.1021/acsami.1c24463 |
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