Formation of 3D tissues of primary hepatocytes using fibrillized collagen microparticles as intercellular binders

被引:4
作者
Morita, Akihiro [1 ]
Yamada, Masumi [1 ]
Utoh, Rie [1 ]
Momiyama, Kanta [1 ]
Iwadate, Hideki [1 ]
Seki, Minoru [1 ]
机构
[1] Chiba Univ, Grad Sch Engn, Dept Appl Chem & Biotechnol, Inage Ku, 1-33 Yayoi Cho, Chiba 2638522, Japan
关键词
Hepatocyte; Collagen; Microparticle; Tissue engineering; Fibril; 3D cell culture; SPHEROID CULTURE; HEPATIC TISSUE; IN-VITRO; LIVER; CELL; FABRICATION; METABOLISM; EXPRESSION; ORGANOIDS; SURVIVAL;
D O I
10.1016/j.jbiosc.2021.11.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Numerous attempts have been made to organize isolated primary hepatocytes into functional three-dimensional (3D) constructs, but technologies to introduce extracellular matrix (ECM) components into such assemblies have not been fully developed. Here we report a new approach to forming hepatocyte-based 3D tissues using fibrillized collagen microparticles (F-CMPs) as intercellular binders. We created thick tissues with a thickness of w200 mm simply by mixing FCMPs with isolated primary rat hepatocytes and culturing them in cell culture inserts. Owing to the incorporated FCMPs, the circular morphology of the formed tissues was stabilized, which was strong enough to be manually manipulated and retrieved from the chamber of the insert. We confirmed that the F-CMPs dramatically improved the cell viability and hepatocyte-specific functions such as albumin production and urea synthesis in the formed tissues. The presented approach provides a versatile strategy for hepatocyte-based tissue engineering, and will have a significant impact on biomedical applications and pharmaceutical research. (c) 2021, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:265 / 272
页数:8
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