Inducible differentiation and morphogenesis of bipotential liver cell lines from wild-type mouse embryos

被引:126
作者
Strick-Marchand, H [1 ]
Weiss, MC [1 ]
机构
[1] Inst Pasteur, Unite Genet Differenciat, CNRS, FRE 2364, F-75724 Paris 15, France
关键词
D O I
10.1053/jhep.2002.36123
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This work shows that hepatic cell lines reproducibly can be derived from E14 embryos of many mouse inbred strains. These bipotential mouse embryonic liver (BMEL) cell lines present a mixed morphology, containing both epithelial and palmate-like cells, and an uncoupled phenotype, expressing hepatocyte transcription factors (HNF1alpha, HNF4alpha, GATA4) but not functions (apolipoproteins, albumin). BMEL cells are bipotential: under inducing conditions they express hepatocyte and bile duct functions. In addition, they can undergo morphogenesis in Matrigel culture to form bile duct units. When returned to basal culture conditions, the differentiated cells revert, within a few days, to an undifferentiated state. The ensemble of markers expressed by BMEL cells implies that they originate from hepatoblasts, the endodermal precursors of the liver. In conclusion, the establishment of a simple and reproducible method to isolate from any mouse embryo bipotential hepatic cell lines that exhibit the properties of transit stem cells provides a novel paradigm for investigation of hepatic cell lineage relationships.
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页码:794 / 804
页数:11
相关论文
共 51 条
[1]   Liver stem cells: a two compartment system [J].
Alison, M .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (06) :710-715
[2]   Transgenic expression in the liver of truncated Met blocks apoptosis and permits immortalization of hepatocytes [J].
Amicone, L ;
Spagnoli, FM ;
Spath, G ;
Giordano, S ;
Tommasini, C ;
Bernardini, S ;
DeLuca, V ;
DellaRocca, C ;
Weiss, MC ;
Comoglio, PM ;
Tripodi, M .
EMBO JOURNAL, 1997, 16 (03) :495-503
[3]   GENE-EXPRESSION IN HEPATOCYTE-LIKE LINES ESTABLISHED BY TARGETED CARCINOGENESIS IN TRANSGENIC MICE [J].
ANTOINE, B ;
LEVRAT, F ;
VALLET, V ;
BERBAR, T ;
CARTIER, N ;
DUBOIS, N ;
BRIAND, P ;
KAHN, A .
EXPERIMENTAL CELL RESEARCH, 1992, 200 (01) :175-185
[4]   SPECIALIZATION SWITCH IN DIFFERENTIATING EMBRYONIC RAT-LIVER PROGENITOR CELLS IN RESPONSE TO SODIUM-BUTYRATE [J].
BLOUIN, MJ ;
LAMY, I ;
LORANGER, A ;
NOEL, M ;
CORLU, A ;
GUGUENGUILLOUZO, C ;
MARCEAU, N .
EXPERIMENTAL CELL RESEARCH, 1995, 217 (01) :22-30
[5]   Liver-enriched transcription factors uncoupled from expression of hepatic functions in hepatoma cell lines [J].
Chaya, D ;
FougereDeschatrette, C ;
Weiss, MC .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6311-6320
[6]   Isolation of functional polarized bile duct units from mouse liver [J].
Cho, WK ;
Mennone, A ;
Boyer, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 280 (02) :G241-G246
[7]  
Clotman F, 2002, DEVELOPMENT, V129, P1819
[8]  
Coffinier C, 2002, DEVELOPMENT, V129, P1829
[9]  
Coleman WB, 1997, AM J PATHOL, V151, P353
[10]   DEVELOPMENT OF DEXAMETHASONE-INDUCIBLE TYROSINE AMINOTRANSFERASE ACTIVITY IN WB-F344 RAT-LIVER EPITHELIAL STEMLIKE CELLS CULTURED IN THE PRESENCE OF SODIUM-BUTYRATE [J].
COLEMAN, WB ;
SMITH, GJ ;
GRISHAM, JW .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 161 (03) :463-469