Published online Apr 14, 2022. doi: 10.3748/wjg.v28.i14.1444
Peer-review started: February 27, 2021
First decision: March 28, 2021
Revised: April 10, 2021
Accepted: September 2, 2021
Article in press: September 2, 2021
Published online: April 14, 2022
Processing time: 403 Days and 6.7 Hours
Liver transplantation is a therapeutic procedure to recover liver function in patients with irreversible liver failure; however, there is currently a shortage of available transplant organs, which limits the availability of this treatment.
Portal branch-ligated (PBL) HPCs are expected to allow regenerative medicine to produce a cell source to provide an alternate source for transplantation.
We aimed to development a liver model using HPCs.
Hepatic stem/progenitor cells have the ability to multiply ex vivo and differentiate into hepatocytes and cholangiocytes. We have previously established HPC lines derived from the hepatic tissues of mice after ligation of venous drainage. In this study, the PBL hepatic lobe-derived HPCs multiplied in a bioreactor chamber to form liver organoid tissues comparable to liver lobules. These organoid tissues were implanted into syngeneic wild-type mice.
In the three-dimensional (3-D) liver tissue culture model, PBL-HPCs differentiated into mature hepatocyte-like cells, in binuclear populations, and with a bile duct–like structure. Quantitative real-time polymerase chain reaction analysis revealed that the cells expressed hepatocyte differentiation markers. In the 3-D liver tissue culture model derived from PBL-HPCs, the levels of urea and albumin production and activities of Cytochrome P450 enzymes were gradually enhanced.
By mimicking the structure of the natural liver, our system was effective for the construction of a functional liver tissue model.
This PBL-derived HPC line has the potential to proliferate, mature, and form implantable hepatic tissue.