Antizyme-dependent and -independent mechanisms are responsible for increased spermidine transport in amino acid-restricted human cancer cells

Biochem Biophys Res Commun. 1999 Mar 24;256(3):646-51. doi: 10.1006/bbrc.1999.0397.

Abstract

Amino acid deprivation can inhibit tumour cell proliferation. Since polyamines are required for cell growth, we hypothesised that their regulatory pathways can respond to amino acid restriction. We report here that exposure of human colon adenocarcinoma Caco-2 cells to a medium restricted for a single amino acid, but not for D-glucose, activates spermidine transport. The increase was rapid and seemed transient with a maximum 4-6 hr after amino acid removal. Kinetics showed that the maximal velocity of transport was solely increased in L-methionine- or L-leucine-deprived cells, indicating increased number of transporters. The intracellular level of complex of ornithine decarboxylase (ODC) with antizyme, a negative regulator of polyamine transport, was decreased by 16-29% in amino acid-deprived cells. However, exposure to limited amounts of amino acid increased transport without altering the ODC-antizyme complex level. We propose that antizyme-independent mechanisms, sensitive to the amino acid concentration, also participate to the control of spermidine transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism*
  • Amino Acids / pharmacology
  • Biological Transport / drug effects
  • Caco-2 Cells
  • Culture Media
  • Cycloheximide / pharmacology
  • Glucose / metabolism
  • Humans
  • Kinetics
  • Polyamines / metabolism
  • Protein Biosynthesis
  • Protein Synthesis Inhibitors / pharmacology
  • Proteins / genetics
  • Proteins / metabolism*
  • RNA, Messenger / metabolism
  • Spermidine / metabolism*

Substances

  • Amino Acids
  • Culture Media
  • Polyamines
  • Protein Synthesis Inhibitors
  • Proteins
  • RNA, Messenger
  • ornithine decarboxylase antizyme
  • Cycloheximide
  • Glucose
  • Spermidine