Cargando…

Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery

The liver plays a central role in metabolism. Although many studies have described in vitro liver models for drug discovery, to date, no model has been described that can stably maintain liver function. Here, we used a unique, scaffold-free 3D bio-printing technology to construct a small portion of...

Descripción completa

Detalles Bibliográficos
Autores principales: Kizawa, Hideki, Nagao, Eri, Shimamura, Mitsuru, Zhang, Guangyuan, Torii, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614670/
https://www.ncbi.nlm.nih.gov/pubmed/28955746
http://dx.doi.org/10.1016/j.bbrep.2017.04.004
_version_ 1783266441818013696
author Kizawa, Hideki
Nagao, Eri
Shimamura, Mitsuru
Zhang, Guangyuan
Torii, Hitoshi
author_facet Kizawa, Hideki
Nagao, Eri
Shimamura, Mitsuru
Zhang, Guangyuan
Torii, Hitoshi
author_sort Kizawa, Hideki
collection PubMed
description The liver plays a central role in metabolism. Although many studies have described in vitro liver models for drug discovery, to date, no model has been described that can stably maintain liver function. Here, we used a unique, scaffold-free 3D bio-printing technology to construct a small portion of liver tissue that could stably maintain drug, glucose, and lipid metabolism, in addition to bile acid secretion. This bio-printed normal human liver tissue maintained expression of several kinds of hepatic drug transporters and metabolic enzymes that functioned for several weeks. The bio-printed liver tissue displayed glucose production via cAMP/protein kinase A signaling, which could be suppressed with insulin. Bile acid secretion was also observed from the printed liver tissue, and it accumulated in the culture medium over time. We observed both bile duct and sinusoid-like structures in the bio-printed liver tissue, which suggested that bile acid secretion occurred via a sinusoid-hepatocyte-bile duct route. These results demonstrated that our bio-printed liver tissue was unique, because it exerted diverse liver metabolic functions for several weeks. In future, we expect our bio-printed liver tissue to be applied to developing new models that can be used to improve preclinical predictions of long-term toxicity in humans, generate novel targets for metabolic liver disease, and evaluate biliary excretion in drug development.
format Online
Article
Text
id pubmed-5614670
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-56146702017-09-27 Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery Kizawa, Hideki Nagao, Eri Shimamura, Mitsuru Zhang, Guangyuan Torii, Hitoshi Biochem Biophys Rep Research Article The liver plays a central role in metabolism. Although many studies have described in vitro liver models for drug discovery, to date, no model has been described that can stably maintain liver function. Here, we used a unique, scaffold-free 3D bio-printing technology to construct a small portion of liver tissue that could stably maintain drug, glucose, and lipid metabolism, in addition to bile acid secretion. This bio-printed normal human liver tissue maintained expression of several kinds of hepatic drug transporters and metabolic enzymes that functioned for several weeks. The bio-printed liver tissue displayed glucose production via cAMP/protein kinase A signaling, which could be suppressed with insulin. Bile acid secretion was also observed from the printed liver tissue, and it accumulated in the culture medium over time. We observed both bile duct and sinusoid-like structures in the bio-printed liver tissue, which suggested that bile acid secretion occurred via a sinusoid-hepatocyte-bile duct route. These results demonstrated that our bio-printed liver tissue was unique, because it exerted diverse liver metabolic functions for several weeks. In future, we expect our bio-printed liver tissue to be applied to developing new models that can be used to improve preclinical predictions of long-term toxicity in humans, generate novel targets for metabolic liver disease, and evaluate biliary excretion in drug development. Elsevier 2017-04-14 /pmc/articles/PMC5614670/ /pubmed/28955746 http://dx.doi.org/10.1016/j.bbrep.2017.04.004 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Kizawa, Hideki
Nagao, Eri
Shimamura, Mitsuru
Zhang, Guangyuan
Torii, Hitoshi
Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title_full Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title_fullStr Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title_full_unstemmed Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title_short Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
title_sort scaffold-free 3d bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614670/
https://www.ncbi.nlm.nih.gov/pubmed/28955746
http://dx.doi.org/10.1016/j.bbrep.2017.04.004
work_keys_str_mv AT kizawahideki scaffoldfree3dbioprintedhumanlivertissuestablymaintainsmetabolicfunctionsusefulfordrugdiscovery
AT nagaoeri scaffoldfree3dbioprintedhumanlivertissuestablymaintainsmetabolicfunctionsusefulfordrugdiscovery
AT shimamuramitsuru scaffoldfree3dbioprintedhumanlivertissuestablymaintainsmetabolicfunctionsusefulfordrugdiscovery
AT zhangguangyuan scaffoldfree3dbioprintedhumanlivertissuestablymaintainsmetabolicfunctionsusefulfordrugdiscovery
AT toriihitoshi scaffoldfree3dbioprintedhumanlivertissuestablymaintainsmetabolicfunctionsusefulfordrugdiscovery