TY - JOUR
T1 - Biotechnology Challenges to In Vitro Maturation of Hepatic Stem Cells
AU - Chen, Chen
AU - Soto-Gutierrez, Alejandro
AU - Baptista, Pedro M.
AU - Spee, Bart
N1 - Funding Information:
Funding This work was supported by grants from the National Institutes of Health (DK099257) to A.S.-G.; Marie Curie Actions (H2020-MSCA-IF-2014 Project #660554), project PI15/00563 and CIBEREHD EH16PI02 from Instituto de Salud Carlos III, Spain to P.M.B.; Dutch Research Council NWO STW (15498) and Dutch Research Council NWO ZON/MW (116004121) to B.S., and China Scholarship Council (CSC201306310019) to C.C.
Publisher Copyright:
© 2018 AGA Institute
PY - 2018/4/1
Y1 - 2018/4/1
N2 - The incidence of liver disease is increasing globally. The only curative therapy for severe end-stage liver disease, liver transplantation, is limited by the shortage of organ donors. In vitro models of liver physiology have been developed and new technologies and approaches are progressing rapidly. Stem cells might be used as a source of liver tissue for development of models, therapies, and tissue-engineering applications. However, we have been unable to generate and maintain stable and mature adult liver cells ex vivo. We review factors that promote hepatocyte differentiation and maturation, including growth factors, transcription factors, microRNAs, small molecules, and the microenvironment. We discuss how the hepatic circulation, microbiome, and nutrition affect liver function, and the criteria for considering cells derived from stem cells to be fully mature hepatocytes. We explain the challenges to cell transplantation and consider future technologies for use in hepatic stem cell maturation, including 3-dimensional biofabrication and genome modification.
AB - The incidence of liver disease is increasing globally. The only curative therapy for severe end-stage liver disease, liver transplantation, is limited by the shortage of organ donors. In vitro models of liver physiology have been developed and new technologies and approaches are progressing rapidly. Stem cells might be used as a source of liver tissue for development of models, therapies, and tissue-engineering applications. However, we have been unable to generate and maintain stable and mature adult liver cells ex vivo. We review factors that promote hepatocyte differentiation and maturation, including growth factors, transcription factors, microRNAs, small molecules, and the microenvironment. We discuss how the hepatic circulation, microbiome, and nutrition affect liver function, and the criteria for considering cells derived from stem cells to be fully mature hepatocytes. We explain the challenges to cell transplantation and consider future technologies for use in hepatic stem cell maturation, including 3-dimensional biofabrication and genome modification.
KW - Culture
KW - Differentiation
KW - Hepatocyte
KW - Liver Development
UR - http://www.scopus.com/inward/record.url?scp=85044592844&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2018.01.066
DO - 10.1053/j.gastro.2018.01.066
M3 - Review article
C2 - 29428334
AN - SCOPUS:85044592844
SN - 0016-5085
VL - 154
SP - 1258
EP - 1272
JO - Gastroenterology
JF - Gastroenterology
IS - 5
ER -