Literature DB >> 203052

A selective system for hepatoma cells producing gluconeogenic enzymes.

R Bertolotti.   

Abstract

Gluconeogenesis is a liver-specific pathway which permits the synthesis of phosphorylated sugars from oxaloacetate, pyruvate, amino acids, or trioses. The absolute requirement for glucose or an alternative hexose which characterizes most mammalian cells probably reflects an inablility to perform gluconeogenesis rather than to generate sufficient energy by respiration alone. Cells of diverse histogenetic origins have been tested in glucose-free medium, supplemented with oxaloacetate or with dihydroxyacetone. The only cells able to grow are well-differentiated hepatoma cells which produce the relevant gluconeogenic enzymes: phosphoenolpyruvate carboxykinase, fructose diphosphatase, and triokinase. Reconstruction experiments demonstrate that glucose-free media permit the selective growth of cells producing gluconeogenic enzymes. These media should be useful for analysis of reexpression of differentiated functions in somatic cell hybrids and for the isolation of mutants.

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Year:  1977        PMID: 203052     DOI: 10.1007/bf01542966

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  11 in total

1.  Liver-enriched transcription factors uncoupled from expression of hepatic functions in hepatoma cell lines.

Authors:  D Chaya; C Fougère-Deschatrette; M C Weiss
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

2.  Tissue-specific expression of the rat albumin gene: genetic control of its extinction in microcell hybrids.

Authors:  C Petit; J Levilliers; M O Ott; M C Weiss
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

3.  Expression of the mouse serum albumin gene introduced into differentiated and dedifferentiated rat hepatoma cells.

Authors:  J Deschatrette; C Fougere-Deschatrette; L Corcos; R T Schimke
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

4.  Liver-specific RNA metabolism in hepatoma cells: variations in transcription rates and mRNA levels.

Authors:  D F Clayton; M Weiss; J E Darnell
Journal:  Mol Cell Biol       Date:  1985-10       Impact factor: 4.272

5.  Genetic analysis of aflatoxin B1 activation in rat hepatoma cells.

Authors:  L Corcos; J P Rousset; F Kiefer; F J Wiebel; M C Weiss
Journal:  Mol Gen Genet       Date:  1990-07

6.  Hepatocyte nuclear factor 4 expression overcomes repression of the hepatic phenotype in dedifferentiated hepatoma cells.

Authors:  G F Späth; M C Weiss
Journal:  Mol Cell Biol       Date:  1997-04       Impact factor: 4.272

7.  A variant nuclear protein in dedifferentiated hepatoma cells binds to the same functional sequences in the beta fibrinogen gene promoter as HNF-1.

Authors:  S Baumhueter; G Courtois; G R Crabtree
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

8.  Tissue-specific expression is conferred by a sequence from the 5' end of the rat albumin gene.

Authors:  M O Ott; L Sperling; P Herbomel; M Yaniv; M C Weiss
Journal:  EMBO J       Date:  1984-11       Impact factor: 11.598

9.  A study of chromosomal changes associated with amplified dihydrofolate reductase genes in rat hepatoma cells and their dedifferentiated variants.

Authors:  C Fougere-Deschatrette; R T Schimke; D Weil; M C Weiss
Journal:  J Cell Biol       Date:  1984-08       Impact factor: 10.539

10.  Angiotensinogen production by rat hepatoma cells in culture and analysis of its regulation by techniques of somatic cell genetics.

Authors:  J Bouhnik; D Cassio; E Coezy; P Corvol; M C Weiss
Journal:  J Cell Biol       Date:  1983-08       Impact factor: 10.539

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