Amsbio reports on the recent publication in Cell by Dr Meritxell Huch, Prof Hans Clevers et al. of ground-breaking research using Cultrex BME2 reduced growth factor (organoid growth matrix) to enable long-term (>1 year) culture of genome-stable bipotent stem cells from adult human liver. These results open up new experimental avenues towards the use of human liver material expanded in vitro as an alternative cell source for disease modeling, toxicology studies, drug testing, regenerative medicine and gene therapy.
Liver diseases (ranging from genetic inherited disorders to viral hepatitis, liver cancer, and obesity-related fatty liver disease) are the twelfth-leading cause of death in the United States. Failure in the management of liver diseases can be attributed to the shortage of donor livers as well as to our poor understanding of the mechanisms behind liver pathology. The value of any cultured cell as a disease model or as a source for cell therapy transplantation depends on the fidelity and robustness of its expansion potential as well as its ability to maintain a normal genetic and epigenetic status.
The research by Huch, Clevers et al. shows that primary human bile duct cells can readily be expanded in vitro as bipotent stem cells into 3D liver organoids using Amsbio’s reduced growth factor basement membrane extract Cultrex BME2 as extracellular matrix (ECM). In this novel culture system, adult liver stem cells maintain their ability of self-renewal; differentiating into functional hepatocyte cells in vitro and generating bona fide hepatocytes upon transplantation. Extensive analysis of the genetic stability of cultured organoids in vitro demonstrates that the expanded cells preserve their genetic integrity over months in culture (agreeing with the authors’ previous observations in a mouse model). Organoids derived from patients with genetic disorders can be used to model liver disease in vitro.
Commenting on this research, Dr. Huch said “We have obtained culture conditions that allow us to long-term expand genetically stable human donor liver cells in organoid culture. One of the clues to this success is the use of ECM that allows the cells to grow in 3D. BME2 has been our ECM of choice for these experiments.”
