Lysosomes: a possible target for psoralen photodamage

P E Høyer, Peter E. Nielsen

17 Citations (Scopus)

Abstract

Treatment in vitro of Ehrlich ascites tumor cells or human fibroblasts with 8-methoxypsoralen (8-MOP, 2.4 microM) and UVA irradiation results in a 30% and 60% respectively reduction in lysosomal beta-galactosidase activity in situ. Under identical conditions one 8-MOP adduct was formed per 2 X 10(4) bases of DNA, one 8-MOP adduct was formed per approximately 10(4) tRNA molecules and one per approximately 100 ribosomes. It is suggested that the decrease in lysosomal beta-galactosidase activity is a result of leakage through the lysosomal membrane caused by psoralen-UVA damage of the lipids in the membrane, since no effect was found on beta-galactosidase in vitro. These results indicate that the lysosomes may also be a target for cellular photodamage by 8-methoxy-psoralen.

Original languageEnglish
JournalJournal of photochemistry and photobiology. B, Biology
Volume3
Issue number3
Pages (from-to)437-47
Number of pages11
ISSN1011-1344
Publication statusPublished - Jun 1989

Keywords

  • Autoradiography
  • Chromatography, Thin Layer
  • DNA/drug effects
  • Fibroblasts/enzymology
  • Humans
  • Lipid Metabolism
  • Lysosomes/drug effects
  • Methoxsalen/pharmacology
  • PUVA Therapy
  • Proteins/metabolism
  • RNA/drug effects
  • Tumor Cells, Cultured/enzymology
  • beta-Galactosidase/metabolism

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