Summary Some key elements of signal transduction have been identified within the nucleus and demonstrated to be responsive to specific
agonists in numerous cell types. In particular, mitogenic stimuli have been reported to induce, a transient increase of the
nuclear phospholipase C β
1 activity, causing the release of inositide-derived second messengers, whereas differentiating stimuli induced a decrease
of the enzyme activity and an increase of nuclear phosphatidylinositol 4,5-bisphosphate (PIP
2). Recently, we reported evidence, in human osteosarcoma Saos-2 cell lines, on the presence of specific nuclear phospholipase
C isoforms and on the activation of phospholipase C β
1 in the nucleus following the exposure to interleukin-1
α. In this study we report immunocytochemical ultrastructural evidence on quantitative variations of PIP
2 and phospholipase C β
1 amounts in the nucleus of Saos-2 cells at different times of exposure to interleukin-1
α. After short periods of culture in the presence of the agonist, the intranuclear amount of PIP
2 is decreased, while a translocation of phospholipase C β
1 occurs from the cytoplasm to the nucleus, in correspondence with the increased hydrolyzing activity of the enzyme. After
longer periods of incubation with interleukin-1
α, on the other hand, the intranuclear amount of PIP
2 is restored to initial level, while the amount of phospholipase C β
1 is increased both at the nuclear and cytoplasmic level, when its activation is no longer effective. The results, compared
with those obtained in other cell types responsive to given agonists, account for a cell-specific modulation of signal transduction
based on polyphosphoinositide breakdown at the nuclear level.
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