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

Authors :
Hideki Kizawa
Eri Nagao
Mitsuru Shimamura
Guangyuan Zhang
Hitoshi Torii
Source :
Biochemistry and Biophysics Reports, Vol 10, Iss C, Pp 186-191 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

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.

Details

Language :
English
ISSN :
24055808
Volume :
10
Issue :
C
Database :
Directory of Open Access Journals
Journal :
Biochemistry and Biophysics Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.276eb7cadc641c59a98341e7367a7dd
Document Type :
article
Full Text :
https://doi.org/10.1016/j.bbrep.2017.04.004