Open AccessBrief exposures of resting fibroblasts to okadaic acid stimulate DNA synthesis
Author(s) -
Setkov N. A.,
Epifanova O. I.
Publication year - 1997
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1046/j.1365-2184.1997.00065.x
Subject(s) - okadaic acid , dna synthesis , 3t3 cells , incubation , stimulation , biology , cell , phosphatase , microbiology and biotechnology , cell culture , incubation period , cell cycle , cell division , dna , transfection , biochemistry , endocrinology , phosphorylation , genetics
To study further the factors providing for cellular quiescence, we used okadaic acid (OA) at concentrations (0.1, 1, 10 or 100 nM) inhibiting type 1 and/or type 2A protein phosphatases in mammalian cell cultures. Brief (2 h) exposure of resting (0.2% serum for 72 h) NIH 3T3 mouse fibroblasts to OA with subsequent incubation of cells in a medium with 0.2% serum, stimulated DNA synthesis at all concentrations studied. Maximal stimulation was observed following pre‐incubation of resting cells with 10 nM OA. Treatment of cycling cells (10% serum) with OA (2 h pulses at 12 h intervals for 72 h) prevented their exit to the resting state on transfer to a medium with 0.2% serum. Brief exposures of resting cells to OA did not affect the rate of protein synthesis. OA pulses in the late pre‐replicative period had no effect on the entry of serum‐stimulated cells into the S phase. Cell fusion experiments with resting (serum‐deprived) and proliferating (serum‐stimulated) NIH 3T3 cells, using radioautography with a double‐labelling technique, revealed that pre‐incubation of resting cells with OA for 2 h before and after fusion abrogates their ability to suppress the onset of DNA synthesis in the nuclei of proliferating cells in heterodikaryons. The results indicate that protein phosphatases of type 1 and/or 2A may be involved in the growth‐arrest machinery that provides for cellular quiescence.