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Macromol Biosci ; 24(5): e2300411, 2024 May.
Article in English | MEDLINE | ID: mdl-38326219

ABSTRACT

Liver fibrosis occurs in many chronic liver diseases, while severe fibrosis can lead to liver failure. A chitosan-phenol based self-healing hydrogel (CP) integrated with decellularized liver matrix (DLM) is proposed in this study as a 3D gel matrix to carry hepatocytes for possible therapy of liver fibrosis. To mimic the physiological liver microenvironment, DLM is extracted from pigs and mixed with CP hydrogel to generate DLM-CP self-healing hydrogel. Hepatocyte spheroids coated with endothelial cells (ECs) are fabricated using a customized method and embedded in the hydrogel. Hepatocytes injured by exposure to CCl4-containing medium are used as the in vitro toxin-mediated liver fibrosis model, where the EC-covered hepatocyte spheroids embedded in the hydrogel are co-cultured with the injured hepatocytes. The urea synthesis of the injured hepatocytes reaches 91% of the normal level after 7 days of co-culture, indicating that the hepatic function of injured hepatocytes is rescued by the hybrid spheroid-laden DLM-CP hydrogel. Moreover, the relative lactate dehydrogenase activity of the injured hepatocytes is decreased 49% by the hybrid spheroid-laden DLM-CP hydrogel after 7 days of co-culture, suggesting reduced damage in the injured hepatocytes. The combination of hepatocyte/EC hybrid spheroids and DLM-CP hydrogel presents a promising therapeutic strategy for hepatic fibrosis.


Subject(s)
Coculture Techniques , Endothelial Cells , Hepatocytes , Hydrogels , Liver , Spheroids, Cellular , Hepatocytes/metabolism , Hepatocytes/cytology , Animals , Spheroids, Cellular/cytology , Hydrogels/chemistry , Hydrogels/pharmacology , Endothelial Cells/cytology , Endothelial Cells/metabolism , Liver/injuries , Liver/pathology , Swine , Decellularized Extracellular Matrix/chemistry , Decellularized Extracellular Matrix/pharmacology , Chitosan/chemistry , Chitosan/pharmacology , Humans , Liver Cirrhosis/pathology , Liver Cirrhosis/therapy , Extracellular Matrix/metabolism , Carbon Tetrachloride
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