TY - JOUR
T1 - Maturation-dependent gene expression in a conditionally transformed liver progenitor cell line
AU - Lemischka, Ihor
AU - Fiorino, A. S.
N1 - DK44266, NIDDK NIH HHS, United StatesR01AA09347, NIAAA NIH HHS, United StatesR29AA08260, NIAAA NIH HHS, United States
PY - 1998
Y1 - 1998
N2 - We have isolated a conditionally transformed liver progenitor cell line with phenotypic similarities to both hepatoblasts (bipotent embryonic liver cells that give rise to hepatocytes and intrahepatic biliary epithelial cells) and liver epithelial cells (primitive hepatic cells isolated from adult livers capable of generating both hepatocytic and biliary lineages). Cell line L2039 was derived from E14 fetal mouse liver after transformation with temperature-sensitive SV-40 large T antigen. At 33°C, these cells have an epithelial morphology with a high nucleocytoplasmic ratio and express both hepatocytic and biliary genes, including albumin, α-fetoprotein, glutamine synthetase, insulin-like growth factor II receptor, fibronectin and laminin, and cytokeratins 8 and 19, a set of markers characteristic for hepatoblasts. The presence of cytokeratin 14, vimentin, and several oval-cell antigens link cell line L2039 to nonparenchymal liver epithelial cell populations thought to contain progenitor cells. Serum-free, hormonally defined media conditions and extracellular matrix requirements were determined for growth and differentiation of this cell line. During culture on type IV collagen at 39°C, L2039 cells cease dividing and demonstrate hepatocytic differentiation with the assumption of a hepatocyte-like morphology and glucocorticoid- dependent regulation of liver-specific genes, including albumin, α- fetoprotein, phosphoenolpyruvate carboxykinase, and liver-enriched transcription factors. The number of albumin-positive cells increases during culture at 39°C, indicating that L2039 cells convert from a prehepatocytic to a hepatocytic phenotype. Under conditions specific for hepatocytic differentiation, C/EBPs were expressed and differentially regulated, with C/EBPβ and C/EBPδ upregulated early and C/EBPα only slightly expressed after 7 d, indicating that C/EBPα may not be a crucial factor in commitment to the hepatocytic phenotype.
AB - We have isolated a conditionally transformed liver progenitor cell line with phenotypic similarities to both hepatoblasts (bipotent embryonic liver cells that give rise to hepatocytes and intrahepatic biliary epithelial cells) and liver epithelial cells (primitive hepatic cells isolated from adult livers capable of generating both hepatocytic and biliary lineages). Cell line L2039 was derived from E14 fetal mouse liver after transformation with temperature-sensitive SV-40 large T antigen. At 33°C, these cells have an epithelial morphology with a high nucleocytoplasmic ratio and express both hepatocytic and biliary genes, including albumin, α-fetoprotein, glutamine synthetase, insulin-like growth factor II receptor, fibronectin and laminin, and cytokeratins 8 and 19, a set of markers characteristic for hepatoblasts. The presence of cytokeratin 14, vimentin, and several oval-cell antigens link cell line L2039 to nonparenchymal liver epithelial cell populations thought to contain progenitor cells. Serum-free, hormonally defined media conditions and extracellular matrix requirements were determined for growth and differentiation of this cell line. During culture on type IV collagen at 39°C, L2039 cells cease dividing and demonstrate hepatocytic differentiation with the assumption of a hepatocyte-like morphology and glucocorticoid- dependent regulation of liver-specific genes, including albumin, α- fetoprotein, phosphoenolpyruvate carboxykinase, and liver-enriched transcription factors. The number of albumin-positive cells increases during culture at 39°C, indicating that L2039 cells convert from a prehepatocytic to a hepatocytic phenotype. Under conditions specific for hepatocytic differentiation, C/EBPs were expressed and differentially regulated, with C/EBPβ and C/EBPδ upregulated early and C/EBPα only slightly expressed after 7 d, indicating that C/EBPα may not be a crucial factor in commitment to the hepatocytic phenotype.
KW - C/EBP
KW - Hepatoblast
KW - Hepatocyte differentiation
KW - SV-40 large T antigen
M3 - Article
C2 - 9557943
SN - 1071-2690
VL - 34
SP - 247
EP - 258
JO - In Vitro Cellular and Developmental Biology - Animal
JF - In Vitro Cellular and Developmental Biology - Animal
IS - 3
ER -