Cargando…
Hep3Gel: A Shape-Shifting Extracellular Matrix-Based, Three-Dimensional Liver Model Adaptable to Different Culture Systems
[Image: see text] Drug-induced hepatotoxicity is a leading cause of clinical trial withdrawal. Therefore, in vitro modeling the hepatic behavior and functionalities is not only crucial to better understand physiological and pathological processes but also to support drug development with reliable hi...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832437/ https://www.ncbi.nlm.nih.gov/pubmed/36525369 http://dx.doi.org/10.1021/acsbiomaterials.2c01226 |
_version_ | 1784868055706238976 |
---|---|
author | Guagliano, Giuseppe Volpini, Cristina Sardelli, Lorenzo Bloise, Nora Briatico-Vangosa, Francesco Cornaglia, Antonia Icaro Dotti, Silvia Villa, Riccardo Visai, Livia Petrini, Paola |
author_facet | Guagliano, Giuseppe Volpini, Cristina Sardelli, Lorenzo Bloise, Nora Briatico-Vangosa, Francesco Cornaglia, Antonia Icaro Dotti, Silvia Villa, Riccardo Visai, Livia Petrini, Paola |
author_sort | Guagliano, Giuseppe |
collection | PubMed |
description | [Image: see text] Drug-induced hepatotoxicity is a leading cause of clinical trial withdrawal. Therefore, in vitro modeling the hepatic behavior and functionalities is not only crucial to better understand physiological and pathological processes but also to support drug development with reliable high-throughput platforms. Different physiological and pathological models are currently under development and are commonly implemented both within platforms for standard 2D cultures and within tailor-made chambers. This paper introduces Hep3Gel: a hybrid alginate–extracellular matrix (ECM) hydrogel to produce 3D in vitro models of the liver, aiming to reproduce the hepatic chemomechanical niche, with the possibility of adapting its shape to different manufacturing techniques. The ECM, extracted and powdered from porcine livers by a specifically set-up procedure, preserved its crucial biological macromolecules and was embedded within alginate hydrogels prior to crosslinking. The viscoelastic behavior of Hep3Gel was tuned, reproducing the properties of a physiological organ, according to the available knowledge about hepatic biomechanics. By finely tuning the crosslinking kinetics of Hep3Gel, its dualistic nature can be exploited either by self-spreading or adapting its shape to different culture supports or retaining the imposed fiber shape during an extrusion-based 3D-bioprinting process, thus being a shape-shifter hydrogel. The self-spreading ability of Hep3Gel was characterized by combining empirical and numerical procedures, while its use as a bioink was experimentally characterized through rheological a priori printability evaluations and 3D printing tests. The effect of the addition of the ECM was evident after 4 days, doubling the survival rate of cells embedded within control hydrogels. This study represents a proof of concept of the applicability of Hep3Gel as a tool to develop 3D in vitro models of the liver. |
format | Online Article Text |
id | pubmed-9832437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98324372023-01-12 Hep3Gel: A Shape-Shifting Extracellular Matrix-Based, Three-Dimensional Liver Model Adaptable to Different Culture Systems Guagliano, Giuseppe Volpini, Cristina Sardelli, Lorenzo Bloise, Nora Briatico-Vangosa, Francesco Cornaglia, Antonia Icaro Dotti, Silvia Villa, Riccardo Visai, Livia Petrini, Paola ACS Biomater Sci Eng [Image: see text] Drug-induced hepatotoxicity is a leading cause of clinical trial withdrawal. Therefore, in vitro modeling the hepatic behavior and functionalities is not only crucial to better understand physiological and pathological processes but also to support drug development with reliable high-throughput platforms. Different physiological and pathological models are currently under development and are commonly implemented both within platforms for standard 2D cultures and within tailor-made chambers. This paper introduces Hep3Gel: a hybrid alginate–extracellular matrix (ECM) hydrogel to produce 3D in vitro models of the liver, aiming to reproduce the hepatic chemomechanical niche, with the possibility of adapting its shape to different manufacturing techniques. The ECM, extracted and powdered from porcine livers by a specifically set-up procedure, preserved its crucial biological macromolecules and was embedded within alginate hydrogels prior to crosslinking. The viscoelastic behavior of Hep3Gel was tuned, reproducing the properties of a physiological organ, according to the available knowledge about hepatic biomechanics. By finely tuning the crosslinking kinetics of Hep3Gel, its dualistic nature can be exploited either by self-spreading or adapting its shape to different culture supports or retaining the imposed fiber shape during an extrusion-based 3D-bioprinting process, thus being a shape-shifter hydrogel. The self-spreading ability of Hep3Gel was characterized by combining empirical and numerical procedures, while its use as a bioink was experimentally characterized through rheological a priori printability evaluations and 3D printing tests. The effect of the addition of the ECM was evident after 4 days, doubling the survival rate of cells embedded within control hydrogels. This study represents a proof of concept of the applicability of Hep3Gel as a tool to develop 3D in vitro models of the liver. American Chemical Society 2022-12-16 2023-01-09 /pmc/articles/PMC9832437/ /pubmed/36525369 http://dx.doi.org/10.1021/acsbiomaterials.2c01226 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 | Guagliano, Giuseppe Volpini, Cristina Sardelli, Lorenzo Bloise, Nora Briatico-Vangosa, Francesco Cornaglia, Antonia Icaro Dotti, Silvia Villa, Riccardo Visai, Livia Petrini, Paola Hep3Gel: A Shape-Shifting Extracellular Matrix-Based, Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title | Hep3Gel:
A Shape-Shifting Extracellular Matrix-Based,
Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title_full | Hep3Gel:
A Shape-Shifting Extracellular Matrix-Based,
Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title_fullStr | Hep3Gel:
A Shape-Shifting Extracellular Matrix-Based,
Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title_full_unstemmed | Hep3Gel:
A Shape-Shifting Extracellular Matrix-Based,
Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title_short | Hep3Gel:
A Shape-Shifting Extracellular Matrix-Based,
Three-Dimensional Liver Model Adaptable to Different Culture Systems |
title_sort | hep3gel:
a shape-shifting extracellular matrix-based,
three-dimensional liver model adaptable to different culture systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832437/ https://www.ncbi.nlm.nih.gov/pubmed/36525369 http://dx.doi.org/10.1021/acsbiomaterials.2c01226 |
work_keys_str_mv | AT guaglianogiuseppe hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT volpinicristina hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT sardellilorenzo hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT bloisenora hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT briaticovangosafrancesco hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT cornagliaantoniaicaro hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT dottisilvia hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT villariccardo hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT visailivia hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems AT petrinipaola hep3gelashapeshiftingextracellularmatrixbasedthreedimensionallivermodeladaptabletodifferentculturesystems |