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

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.

Automated summary

This study reports a new approach using fibrillized collagen microparticles (F-CMPs) as intercellular binders to form hepatocyte-based 3D tissues. Thick and stable tissues were successfully created by mixing these microparticles with hepatocytes, with a thickness of approximately 200 microns. The incorporation of F-CMPs improved cell viability and hepatocyte-specific functions, demonstrating the significance of this method for hepatocyte-based tissue engineering.