Cytoplasmic and nuclear localization sites of phosphatidylinositol 3-kinase in human osteosarcoma sensitive and multidrug-resistant Saos-2 cells

Nicoletta Zini, Andrea Ognibene, Alberto Bavelloni, Spartaco Santi, Patrizia Sabatelli, Nicola Baldini, Katia Scotlandi, Massimo Serra, Nadir Mario Maraldi

Research output: Contribution to journalArticle

Abstract

The intracellular localization of phosphatidylinositol 3-kinase (PI 3-kinase) has been analyzed by western blotting, confocal, and electron microscopy immunocytochemistry in human osteosarcoma Saos-2 cells. By western blotting, the enzyme appears to be present in both the cytoplasmic and nuclear subfractions. By confocal microscope immunocytochemistry, the cytoplasmic fluorescence is localized in the perinuclear region and on a network of filaments, while a diffused signal is present in the nucleus, except for the nucleolar areas. Ultrastructural analyses on whole cells and on in situ matrix preparations reveal that nuclear PI 3-kinase is localized in interchromatin domains, in stable association with inner nuclear matrix components, while the enzyme diffused in the cytosol is partly associated with the cytoskeletal filaments. Quantitative evaluations indicate that, in a multidrug-resistant variant obtained by continuous exposure of Saos-2 cells to doxorubicin, the amount of nuclear and cytoplasmic PI 3-kinase is significantly lower than in the sensitive parental cell line. The nuclear localization of PI 3-kinase and its variation in multidrug-resistant cells, characterized by a reduced mitotic index, are consistent with the data on the existence of a nuclear inositol lipid cycle, which could also utilize 3-phosphorylated inositides to modulate signal transduction for the control of some key functional activities.

Original languageEnglish
Pages (from-to)457-464
Number of pages8
JournalHistochemistry and Cell Biology
Volume106
Issue number5
DOIs
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Cell Biology
  • Molecular Biology
  • Histology
  • Instrumentation
  • Medical Laboratory Technology

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