C/EBPα and C/EBPβ are markers of early liver development

被引:45
作者
Westmacott, Adam
Burke, Zoe D.
Oliver, Guillermo
Slack, Jonathan M. W.
Tosh, David [1 ]
机构
[1] Univ Bath, Ctr Regenerat Med, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
[2] St Jude Childrens Hosp, Dept Genet & Tumour Cell Biol, Memphis, TN 38105 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
C/EBP; HNF4; alpha-fetoprotein (AFP); Pdx1; liver development;
D O I
10.1387/ijdb.062146aw
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pancreatic cells can be converted to hepatocytes by overexpression of C/EBP beta (Shen, C-N, Slack, J.M.W. and Tosh, D., 2000. Molecular basis of transdifferentiation of pancreas to liver. Nature Cell Biology2: 879-887). This suggested that expression of one or more C/EBP factors may distinguish liver and pancreas in early development. We have now studied the early expression of C/EBP alpha and C/EBP beta in the mouse embryo and show that both are expressed exclusively in the early liver bud and not in the pancreatic buds. Their expression is identical to that of hepatocyte nuclear factor 4 (HNF4), another key hepatic transcription factor and alpha-fetoprotein (AFP), a differentiation product characteristic of immature hepatocytes. Both are complementary to the early expression of Pdx1, a key pancreatic transcription factor. These results are consistent with the idea that C/EBP factors are master regulators for liver development.
引用
收藏
页码:653 / 657
页数:5
相关论文
共 35 条
[11]   Disruption of hepatic C/EBPα results in impaired glucose tolerance and age-dependent hepatosteatosis [J].
Inoue, Y ;
Inoue, J ;
Lambert, G ;
Yim, SH ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (43) :44740-44748
[12]   Quantitative gene expression profiling reveals a fetal hepatic phenotype of murine ES-derived hepatocytes [J].
Jochheim, A ;
Hillemann, T ;
Kania, G ;
Scharf, J ;
Attaran, M ;
Manns, MP ;
Wobus, AM ;
Ott, M .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2004, 48 (01) :23-29
[13]   INSULIN-PROMOTER-FACTOR-1 IS REQUIRED FOR PANCREAS DEVELOPMENT IN MICE [J].
JONSSON, J ;
CARLSSON, L ;
EDLUND, T ;
EDLUND, H .
NATURE, 1994, 371 (6498) :606-609
[14]   Initiation of mammalian liver development from endoderm by fibroblast growth factors [J].
Jung, JN ;
Zheng, MH ;
Goldfarb, M ;
Zaret, KS .
SCIENCE, 1999, 284 (5422) :1998-2003
[15]   Induction and regulation of acute phase proteins in transdifferentiated hepatocytes [J].
Kurash, JK ;
Shen, CN ;
Tosh, D .
EXPERIMENTAL CELL RESEARCH, 2004, 292 (02) :342-358
[16]  
LEDOUARIN NM, 1975, MED BIOL, V53, P427
[17]   The initiation of liver development is dependent on Foxa transcription factors [J].
Lee, CS ;
Friedman, JR ;
Fulmer, JT ;
Kaestner, KH .
NATURE, 2005, 435 (7044) :944-947
[18]   Biological role of the CCAAT enhancer-binding protein family of transcription factors [J].
Lekstrom-Himes, J ;
Xanthopoulos, KG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :28545-28548
[19]  
Liu S, 1998, DIABETES, V47, pA295
[20]   Molecular cloning, genetic mapping, and expression analysis of four zebrafish c/ebp genes [J].
Lyons, SE ;
Shue, BC ;
Lei, L ;
Oates, AC ;
Zon, LI ;
Liu, PP .
GENE, 2001, 281 (1-2) :43-51