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3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro

In recent years 3D-bioprinting technology has been developed as an alternative to animal testing. It possesses a great potential for in vitro testing as it aims to mimic human organs and physiology. In the present study, an alginate-gelatin-Matrigel based hydrogel was used to prepare 3D-bioprinted H...

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Autores principales: Schmidt, Konrad, Berg, Johanna, Roehrs, Viola, Kurreck, Jens, Al-Zeer, Munir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708771/
https://www.ncbi.nlm.nih.gov/pubmed/33304827
http://dx.doi.org/10.1016/j.toxrep.2020.11.003
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author Schmidt, Konrad
Berg, Johanna
Roehrs, Viola
Kurreck, Jens
Al-Zeer, Munir A.
author_facet Schmidt, Konrad
Berg, Johanna
Roehrs, Viola
Kurreck, Jens
Al-Zeer, Munir A.
author_sort Schmidt, Konrad
collection PubMed
description In recent years 3D-bioprinting technology has been developed as an alternative to animal testing. It possesses a great potential for in vitro testing as it aims to mimic human organs and physiology. In the present study, an alginate-gelatin-Matrigel based hydrogel was used to prepare 3D-bioprinted HepaRG cultures using a pneumatic extrusion printer. These 3D models were tested for viability and metabolic functions. Using 3D-bioprinted HepaRG cultures, we tested the toxicity of aflatoxin B1 (10 or 20 μM) in vitro and compared the results with 2D HepaRG cultures. There was a dose-dependent toxicity effect on cell viability, reduction of metabolic activity and albumin production. We found that 3D-bioprinted HepaRG cultures are more resistant to aflatoxin B1 treatment than 2D cultures. Although the metabolic activities were reduced upon treatment with aflatoxin B1, the 3D models were still viable and survived longer, up to 3 weeks, than the 2D culture, as visualized by fluorescence microscopy. Furthermore, albumin production recovered slightly in 3D models after one and two weeks of treatment. Taken together, we consider using 3D-bioprinting technology to generate 3D tissue models as an alternative way to study toxicity in vitro and this could also provide a suitable alternative for chronic hepatotoxicity studies in vitro.
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spelling pubmed-77087712020-12-09 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro Schmidt, Konrad Berg, Johanna Roehrs, Viola Kurreck, Jens Al-Zeer, Munir A. Toxicol Rep A vision for the future of pesticide toxicology In recent years 3D-bioprinting technology has been developed as an alternative to animal testing. It possesses a great potential for in vitro testing as it aims to mimic human organs and physiology. In the present study, an alginate-gelatin-Matrigel based hydrogel was used to prepare 3D-bioprinted HepaRG cultures using a pneumatic extrusion printer. These 3D models were tested for viability and metabolic functions. Using 3D-bioprinted HepaRG cultures, we tested the toxicity of aflatoxin B1 (10 or 20 μM) in vitro and compared the results with 2D HepaRG cultures. There was a dose-dependent toxicity effect on cell viability, reduction of metabolic activity and albumin production. We found that 3D-bioprinted HepaRG cultures are more resistant to aflatoxin B1 treatment than 2D cultures. Although the metabolic activities were reduced upon treatment with aflatoxin B1, the 3D models were still viable and survived longer, up to 3 weeks, than the 2D culture, as visualized by fluorescence microscopy. Furthermore, albumin production recovered slightly in 3D models after one and two weeks of treatment. Taken together, we consider using 3D-bioprinting technology to generate 3D tissue models as an alternative way to study toxicity in vitro and this could also provide a suitable alternative for chronic hepatotoxicity studies in vitro. Elsevier 2020-11-21 /pmc/articles/PMC7708771/ /pubmed/33304827 http://dx.doi.org/10.1016/j.toxrep.2020.11.003 Text en © 2020 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 A vision for the future of pesticide toxicology
Schmidt, Konrad
Berg, Johanna
Roehrs, Viola
Kurreck, Jens
Al-Zeer, Munir A.
3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title_full 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title_fullStr 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title_full_unstemmed 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title_short 3D-bioprinted HepaRG cultures as a model for testing long term aflatoxin B1 toxicity in vitro
title_sort 3d-bioprinted heparg cultures as a model for testing long term aflatoxin b1 toxicity in vitro
topic A vision for the future of pesticide toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708771/
https://www.ncbi.nlm.nih.gov/pubmed/33304827
http://dx.doi.org/10.1016/j.toxrep.2020.11.003
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