Literature DB >> 6306018

Adenosine metabolism in wild-type and enzyme-deficient variants of Chinese hamster ovary and Novikoff rat hepatoma cells.

P G Plagemann, R M Wohlhueter.   

Abstract

Variants of Chinese hamster ovary and Novikoff rat hepatoma cells resistant to tubercidin and 2,5-diaminopurine, or to both drugs, were isolated, and their ability to convert adenosine and various adenosine analogs to nucleotides was compared to that of wild-type cells, both in intact cells and cell-free extracts. Adenosine deamination, and thus its conversion to nucleotides via inosine-hypoxanthine-inosine monophosphate, was inhibited by pretreatment of the cells or cell extracts with 2-deoxycoformycin. Cell-free extracts of the tubercidin-resistant variants, as well as of two adenosine-resistant mutants of Chinese hamster ovary cells, phosphorylated adenosine, tubercidin, pyrazofurin, or tricyclic nucleoside in the presence of ATP at less than 1% of the rate of extracts of wild-type cells. However, addition of phosphoribosyl pyrophosphate stimulated the conversion of adenosine to nucleotides 40-fold. Similarly, intact adenosine kinase-deficient cells failed to phosphorylate the adenosine analogs, but still converted adenosine to nucleotides at 5-10% the rate observed with wild-type cells. Phosphorylation of adenosine and tubercidin in wild-type cells was inhibited by substrate at concentration above 5-10 microM. In contrast, the rate of conversion of adenosine to nucleotides by adenosine kinase-deficient cells increased linearly up to a concentration of 400 microM adenosine, with the consequence that, at this concentration, these cells took up adenosine almost as rapidly as wild-type cells. Adenosine uptake by these kinase-deficient cells was inhibited by adenine and 5'-deoxyadenosine, and was largely abolished in mutants devoid also of adenine phosphoribosyltransferase. We conclude that adenosine is converted to nucleotides in adenosine kinase-deficient cells via adenine. Indirect evidence implicates 5'-methylthioadenosine phosphorylase as the enzyme responsible for the degradation of adenosine to adenine.

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Year:  1983        PMID: 6306018     DOI: 10.1002/jcp.1041160216

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  5 in total

1.  Differential inhibition of 2'-deoxycytidine salvage as a possible mechanism for potentiation of the anti-human immunodeficiency virus activity of 2',3'-dideoxycytidine by dipyridamole.

Authors:  S S Patel; J Szebeni; L M Wahl; J N Weinstein
Journal:  Antimicrob Agents Chemother       Date:  1991-06       Impact factor: 5.191

2.  Hypoxanthine transport in mammalian cells: cell type-specific differences in sensitivity to inhibition by dipyridamole and uridine.

Authors:  P G Plagemann; R M Wohlhueter
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

3.  Interaction of [3H]dipyridamole with the nucleoside transporters of human erythrocytes and cultured animal cells.

Authors:  C Woffendin; P G Plagemann
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

4.  Residual nitrobenzylthioinosine-resistant nucleoside transport in a transport mutant (AE1) of S49 murine T-lymphoma cells.

Authors:  P G Plagemann; C Woffendin
Journal:  Mol Cell Biol       Date:  1987-01       Impact factor: 4.272

5.  Mechanism and control of degradation and resynthesis of adenylates in tumour cells.

Authors:  Z Kovacević; O Brkljac; D Jerance
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

  5 in total

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