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Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning

Solution blow spinning (SBS) has recently emerged as a novel method that can produce nano- and microfiber structures suitable for tissue engineering. Gelatin is an excellent precursor for SBS as it is derived mainly from collagens that are abundant in natural extracellular matrices. Here we report,...

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Autores principales: Klaas, Mariliis, Möll, Kaidi, Mäemets-Allas, Kristina, Loog, Mart, Järvekülg, Martin, Jaks, Viljar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505433/
https://www.ncbi.nlm.nih.gov/pubmed/34635750
http://dx.doi.org/10.1038/s41598-021-99659-1
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author Klaas, Mariliis
Möll, Kaidi
Mäemets-Allas, Kristina
Loog, Mart
Järvekülg, Martin
Jaks, Viljar
author_facet Klaas, Mariliis
Möll, Kaidi
Mäemets-Allas, Kristina
Loog, Mart
Järvekülg, Martin
Jaks, Viljar
author_sort Klaas, Mariliis
collection PubMed
description Solution blow spinning (SBS) has recently emerged as a novel method that can produce nano- and microfiber structures suitable for tissue engineering. Gelatin is an excellent precursor for SBS as it is derived mainly from collagens that are abundant in natural extracellular matrices. Here we report, for the first time the successful generation of 3D thermally crosslinked preforms by using SBS from porcine gelatin. These SBS mats were shown to have three-dimensional fibrous porous structure similar to that of mammalian tissue extracellular matrix. In pharma industry, there is an urgent need for adequate 3D liver tissue models that could be used in high throughput setting for drug screening and to assess drug induced liver injury. We used SBS mats as culturing substrates for human hepatocytes to create an array of 3D human liver tissue equivalents in 96-well format. The SBS mats were highly cytocompatible, facilitated the induction of hepatocyte specific CYP gene expression in response to common medications, and supported the maintenance of hepatocyte differentiation and polarization status in long term cultures for more than 3 weeks. Together, our results show that SBS-generated gelatin scaffolds are a simple and efficient platform for use in vitro for drug testing applications.
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spelling pubmed-85054332021-10-13 Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning Klaas, Mariliis Möll, Kaidi Mäemets-Allas, Kristina Loog, Mart Järvekülg, Martin Jaks, Viljar Sci Rep Article Solution blow spinning (SBS) has recently emerged as a novel method that can produce nano- and microfiber structures suitable for tissue engineering. Gelatin is an excellent precursor for SBS as it is derived mainly from collagens that are abundant in natural extracellular matrices. Here we report, for the first time the successful generation of 3D thermally crosslinked preforms by using SBS from porcine gelatin. These SBS mats were shown to have three-dimensional fibrous porous structure similar to that of mammalian tissue extracellular matrix. In pharma industry, there is an urgent need for adequate 3D liver tissue models that could be used in high throughput setting for drug screening and to assess drug induced liver injury. We used SBS mats as culturing substrates for human hepatocytes to create an array of 3D human liver tissue equivalents in 96-well format. The SBS mats were highly cytocompatible, facilitated the induction of hepatocyte specific CYP gene expression in response to common medications, and supported the maintenance of hepatocyte differentiation and polarization status in long term cultures for more than 3 weeks. Together, our results show that SBS-generated gelatin scaffolds are a simple and efficient platform for use in vitro for drug testing applications. Nature Publishing Group UK 2021-10-11 /pmc/articles/PMC8505433/ /pubmed/34635750 http://dx.doi.org/10.1038/s41598-021-99659-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Klaas, Mariliis
Möll, Kaidi
Mäemets-Allas, Kristina
Loog, Mart
Järvekülg, Martin
Jaks, Viljar
Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title_full Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title_fullStr Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title_full_unstemmed Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title_short Long-term maintenance of functional primary human hepatocytes in 3D gelatin matrices produced by solution blow spinning
title_sort long-term maintenance of functional primary human hepatocytes in 3d gelatin matrices produced by solution blow spinning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505433/
https://www.ncbi.nlm.nih.gov/pubmed/34635750
http://dx.doi.org/10.1038/s41598-021-99659-1
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