TY - JOUR
T1 - Hepatocyte-like cells derived from induced pluripotent stem cells
AU - Roy-Chowdhury, Namita
AU - Wang, Xia
AU - Guha, Chandan
AU - Roy-Chowdhury, Jayanta
N1 - Publisher Copyright:
© 2016, Asian Pacific Association for the Study of the Liver.
PY - 2017/1/1
Y1 - 2017/1/1
N2 - The discovery that coordinated expression of a limited number of genes can reprogram differentiated somatic cells to induced pluripotent stem cells (iPSC) has opened novel possibilities for developing cell-based models of diseases and regenerative medicine utilizing cell reprogramming or cell transplantation. Directed differentiation of iPSCs can potentially generate differentiated cells belonging to any germ layer, including cells with hepatocyte-like morphology and function. Such cells, termed iHeps, can be derived by sequential cell signaling using available information on embryological development or by forced expression of hepatocyte-enriched transcription factors. In addition to the translational aspects of iHeps, the experimental findings have provided insights into the mechanisms of cell plasticity that permit one cell type to transition to another. However, iHeps generated by current methods do not fully exhibit all characteristics of mature hepatocytes, highlighting the need for additional research in this area. Here we summarize the current approaches and achievements in this field and discuss some existing hurdles and emerging approaches for improving iPSC differentiation, as well as maintaining such cells in culture for increasing their utility in disease modeling and drug development.
AB - The discovery that coordinated expression of a limited number of genes can reprogram differentiated somatic cells to induced pluripotent stem cells (iPSC) has opened novel possibilities for developing cell-based models of diseases and regenerative medicine utilizing cell reprogramming or cell transplantation. Directed differentiation of iPSCs can potentially generate differentiated cells belonging to any germ layer, including cells with hepatocyte-like morphology and function. Such cells, termed iHeps, can be derived by sequential cell signaling using available information on embryological development or by forced expression of hepatocyte-enriched transcription factors. In addition to the translational aspects of iHeps, the experimental findings have provided insights into the mechanisms of cell plasticity that permit one cell type to transition to another. However, iHeps generated by current methods do not fully exhibit all characteristics of mature hepatocytes, highlighting the need for additional research in this area. Here we summarize the current approaches and achievements in this field and discuss some existing hurdles and emerging approaches for improving iPSC differentiation, as well as maintaining such cells in culture for increasing their utility in disease modeling and drug development.
KW - Cell transplantation
KW - Cellular models of disease
KW - Directed differentiation
KW - Hepatocyte-like cells
KW - Reprogramming
KW - iPS cells
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U2 - 10.1007/s12072-016-9757-y
DO - 10.1007/s12072-016-9757-y
M3 - Review article
C2 - 27530815
AN - SCOPUS:84982106561
SN - 1936-0533
VL - 11
SP - 54
EP - 69
JO - Hepatology International
JF - Hepatology International
IS - 1
ER -