Abstract

Sphingosine, a breakdown product of cellular sphingolipids, has recently been shown to stimulate DNA synthesis and act synergistically with known growth factors to induce proliferation of quiescent Swiss 3T3 fibroblasts (Hong, Z., Buckley, N. E., Gibson, K., and Spiegel, S. (1990) J. Biol. Chem. 265, 76-81). The present study demonstrates that mitogenic concentrations of sphingosine induce early increases in cytosolic phosphatidic acid, which is a potent mitogen for Swiss 3T3 cells. Structurally related analogs of sphingosine, such as N-stearoylsphingosine and other long chain aliphatic amines, did not mimic the mitogenic effect of sphingosine and did not elevate phosphatidic acid levels. Sphingosine not only stimulated [3H]thymidine incorporation with similar efficiency and kinetics as phosphatidic acid, it also induced similar morphological alterations. Both sphingosine and phosphatidic acid acted synergistically with a variety of growth factors, such as, insulin, epidermal growth factor, fibroblast growth factor, and 12-O-tetradecanoylphorbol 13-acetate. In sharp contrast, sphingosine and phosphatidic acid did not have additive or synergistic effects in either the presence or absence of other growth factors. Both sphingosine and phosphatidic acid stimulated DNA synthesis in cells made protein kinase C-deficient by prolonged treatment with phorbol ester and sphingosine still stimulated similar increases in phosphtidic acid in these cells. Furthermore, similar to the actions of phosphatidic acid on signal transduction in Swiss 3T3 cells, mitogenic concentrations of sphingosine also inhibit cAMP accumulation and trigger the hydrolysis of polyphosphoinositides. Our findings indicate that sphingosine and phosphatidic acid control cellular responses in Swiss 3T3 cells through a common pathway. In view of the prominent role of phosphatidic acid in signal transduction and cellular proliferation, our observations that sphingosine, at mitogenic concentrations, increases the level of phosphatidic acid and also mimics the effects of phosphatidic acid on signal transduction, have important implications for the mechanism of action of sphingosine.

Highlights

  • Sphingosine, a breakdown product of cellular sphingolipids, has recently been shown to stimulate DNA synthesis and act synergistically with known growth factors to induce proliferation of quiescent Swiss 3T3 fibroblasts

  • Our results show closely linked early changes in cytosolic phosphatidic acid levels, consistent with previous studies demonstrating that phosphatidic acid is a potent mitogen for Swiss 3T3 cells and suggest that at least part of the mitogenicity induced by sphingosine may be mediated by a rapid rise in phosphatidic acid

  • We found that the time course of the increase in DNA synthesis in quiescent cultures of Swiss 3T3 cells induced by sphingosine treatment was essentially the same as that induced in response to phosphatidic acid

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Summary

Both sphingosine and phosphatidic acid stimulated

DNA synthesis in cells made protein kinase C-deficient by prolonged treatment with phorbol ester and sphingosine still stimulated similar increases in phosphatidic acid in these cells. Our findings indicate that sphingosine and phosphatidic acid control cellular responses in Swiss 3T3 cells through a common pathway. In view of the prominent role of phosphatidic acid in signal transduction and cellular proliferation, our observations that sphingosine, at mitogenic concentrations, increases the level of phosphatidic acid and mimics the effects of phosphatidic acid on signal transduction, have important implications for the mechanism of action of sphingosine. 3T3 fibroblasts and potentiate the mitogenic responses to other growth factors via a protein kinase C-independent pathway [19] This raises the intriguing possibility that these breakdown products of cellular sphingolipids may play an important role as positive modulators of cell growth acting in a fundamentally different, protein kinase C-independent pathway and that the other target(s) of sphingosine action still remains to be uncovered. Our results show closely linked early changes in cytosolic phosphatidic acid levels, consistent with previous studies demonstrating that phosphatidic acid is a potent mitogen for Swiss 3T3 cells and suggest that at least part of the mitogenicity induced by sphingosine may be mediated by a rapid rise in phosphatidic acid

PROCEDURES
Measurement of Phosphoinositide
RESULTS
TABLE I
Effect of Sphingosine on DNA Synthesis and Phosphatidic
Lack of Effect of Sphingosine Analogs on Phosphatidic Acid
TABLE III
Confluent and quiescent cultures of
Mitogenicity and Phosphatidic Acid
TABLE IV
TABLE V
Full Text
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