Literature DB >> 3170445

Quantitative studies of amino acid and growth factor requirements of transformed and nontransformed cells in high concentrations of serum or lymph.

T Nomura1, H Rubin.   

Abstract

The growth rate of spontaneously transformed BALB/3T3 cells is proportional to glutamine concentration between 50 and 400 microM, with little or no growth occurring in less than 50 microM glutamine. By contrast, nontransformed BALB/3T3 cells multiply, although slowly, with as little as 20 microM glutamine. Neither cell type depletes the medium of glutamine at the low concentrations. Cystine requirements of both cell types increase with serum concentration, probably due to the binding of half-cystine residues by the serum. Calf serum is a much more potent stimulator of cell multiplication than calf lymph, especially for the nontransformed cells. The rate of cell multiplication can be reduced by lowering the concentration of essential amino acids to the physiologic level found in body fluids, but the growth limitations can be fully compensated by simply raising the serum concentration. Growth factors may act by enhancing the utilization of amino acids, particularly of glutamine which is a required substrate for the first and chief regulatory steps of purine and pyrimidine synthesis. Lymph, which is coextensive with interstitial fluid in vivo, is poor in growth factors for the nontransformed BALB/3T3 cells as well as for recently explanted mouse embryo cells, which raises questions of how normal cell growth is maintained in the body.

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Year:  1988        PMID: 3170445     DOI: 10.1007/bf02623897

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  20 in total

1.  The reversible binding of half-cystine residues to serum protein, and its bearing on the cystine requirement of cultured mammalian cells.

Authors:  H EAGLE; V I OYAMA; K A PIEZ
Journal:  J Biol Chem       Date:  1960-06       Impact factor: 5.157

2.  Nucleotide and pentose synthesis after serum-stimulation of resting 3T6 fibroblasts.

Authors:  M L Smith; J M Buchanan
Journal:  J Cell Physiol       Date:  1979-11       Impact factor: 6.384

3.  Glutaminase activities in normal and neoplastic tissues of the rat.

Authors:  W E Knox; G C Tremblay; B B Spanier; G H Friedell
Journal:  Cancer Res       Date:  1967-08       Impact factor: 12.701

4.  Control of pyrimidine biosynthesis in mammalian tissues. I. Partial purification and characterization of glutamine-utilizing carbamyl phosphate synthetase of mouse spleen and its tissue distribution.

Authors:  M Tatibana; K Ito
Journal:  J Biol Chem       Date:  1969-10-10       Impact factor: 5.157

5.  Critical adjustment of cysteine and glutamine concentrations for improved clonal growth of WI-38 cells.

Authors:  R G Ham; S L Hammond; L L Miller
Journal:  In Vitro       Date:  1977-01

6.  Evidence that glutamine, not sugar, is the major energy source for cultured HeLa cells.

Authors:  L J Reitzer; B M Wice; D Kennell
Journal:  J Biol Chem       Date:  1979-04-25       Impact factor: 5.157

7.  Improved medium and culture conditions for clonal growth with minimal serum protein and for enhanced serum-free survival of Swiss 3T3 cells.

Authors:  G D Shipley; R G Ham
Journal:  In Vitro       Date:  1981-08

8.  Use of lymph in cell culture to model hormonal and nutritional constraints on tumor growth in vivo.

Authors:  H Rubin; T Nomura
Journal:  Cancer Res       Date:  1987-09-15       Impact factor: 12.701

9.  Selection and adaptation for rapid growth in culture of cells from delayed sarcomas in nude mice.

Authors:  H Rubin; B M Chu; P Arnstein
Journal:  Cancer Res       Date:  1987-01-15       Impact factor: 12.701

10.  Dynamics of tumor growth and cellular adaptation after inoculation into nude mice of varying numbers of transformed 3T3 cells and of readaptation to culture of the tumor cells.

Authors:  H Rubin; B M Chu; P Arnstein
Journal:  Cancer Res       Date:  1986-04       Impact factor: 12.701

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  2 in total

1.  Deprivation of glutamine in cell culture reveals its potential for treating cancer.

Authors:  Harry Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  2019-03-15       Impact factor: 11.205

2.  Susceptibility to cytotoxic T lymphocyte-induced apoptosis is a function of the proliferative status of the target.

Authors:  W K Nishioka; R M Welsh
Journal:  J Exp Med       Date:  1994-02-01       Impact factor: 14.307

  2 in total

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