Development of Liver Decellularized Extracellular Matrix Bioink for Three-Dimensional Cell Printing-Based Liver Tissue Engineering

• Published in: Biomacromolecules Vol. 18; no. 4; pp. 1229 - 1237
• Main Authors: Lee, Hyungseok, Han, Wonil, Kim, Hyeonji, Ha, Dong-Heon, Jang, Jinah, Kim, Byoung Soo, Cho, Dong-Woo
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 10.04.2017
• Subjects: Animals; biocompatible materials; Biocompatible Materials - chemistry; bioprinting; Bioprinting - methods; Bone Marrow Cells - cytology; Cell Differentiation; Cell Survival; collagen; Collagen - chemistry; drugs; extracellular matrix; Extracellular Matrix - metabolism; Hep G2 Cells; human cell lines; Humans; liver; Liver - cytology; liver failure; Mesenchymal Stromal Cells - cytology; Printing, Three-Dimensional; screening; stem cells; Swine; tissue engineering; Tissue Engineering - methods; Tissue Scaffolds - chemistry
• ISSN: 1525-7797; 1526-4602; 1526-4602
• DOI: 10.1021/acs.biomac.6b01908

The liver is an important organ and plays major roles in the human body. Because of the lack of liver donors after liver failure and drug-induced liver injury, much research has focused on developing liver alternatives and liver in vitro models for transplantation and drug screening. Although numerous studies have been conducted, these systems cannot faithfully mimic the complexity of the liver. Recently, three-dimensional (3D) cell printing technology has emerged as one of a number of innovative technologies that may help to overcome this limitation. However, a great deal of work in developing biomaterials optimized for 3D cell printing-based liver tissue engineering remains. Therefore, in this work, we developed a liver decellularized extracellular matrix (dECM) bioink for 3D cell printing applications and evaluated its characteristics. The liver dECM bioink retained the major ECM components of the liver while cellular components were effectively removed and further exhibited suitable and adjustable properties for 3D cell printing. We further studied printing parameters with the liver dECM bioink to verify the versatility and fidelity of the printing process. Stem cell differentiation and HepG2 cell functions in the liver dECM bioink in comparison to those of commercial collagen bioink were also evaluated, and the liver dECM bioink was found to induce stem cell differentiation and enhance HepG2 cell function. Consequently, the results demonstrate that the proposed liver dECM bioink is a promising bioink candidate for 3D cell printing-based liver tissue engineering.