Sphingosine-1-phosphate (SPP) is a bioactive lipid that has recently been identified as the ligand for the EDG family of G protein–coupled cell surface receptors. However, the mitogenic and survival effects of exogenous SPP may not correlate with binding to cell-surface receptors (Van Brocklyn, J.R., M.J. Lee, R. Menzeleev, A. Olivera, L. Edsall, O. Cuvillier, D.M. Thomas, P.J.P. Coopman, S. Thangada, T. Hla, and S. Spiegel. 1998. J. Cell Biol. 142:229–240). The recent cloning of sphingosine kinase, a unique lipid kinase responsible for the formation of SPP, has provided a new tool to investigate the role of intracellular SPP. Expression of sphingosine kinase markedly increased SPP levels in NIH 3T3 fibroblasts and HEK293 cells, but no detectable secretion of SPP into the medium was observed. The increased sphingosine kinase activity in NIH 3T3 fibroblasts was sufficient to promote growth in low- serum media, expedite the G1/S transition, and increase DNA synthesis and the proportion of cells in the S phase of the cell cycle with a concomitant increase in cell numbers. Transient or stable overexpression of sphingosine kinase in NIH 3T3 fibroblasts or HEK293 cells protected against apoptosis induced by serum deprivation or ceramide elevation. N,N-Dimethylsphingosine, a competitive inhibitor of sphingosine kinase, blocked the effects of sphingosine kinase overexpression on cell proliferation and suppression of apoptosis. In contrast, pertussis toxin did not abrogate these biological responses. In Jurkat T cells, overexpression of sphingosine kinase also suppressed serum deprivation- and ceramide-induced apoptosis and, to a lesser extent, Fas-induced apoptosis, which correlated with inhibition of DEVDase activity, as well as inhibition of the executionary caspase-3. Taken together with ample evidence showing that growth and survival factors activate sphingosine kinase, our results indicate that SPP functions as a second messenger important for growth and survival of cells. Hence, SPP belongs to a novel class of lipid mediators that can function inside and outside cells.
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1 November 1999
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November 01 1999
Sphingosine Kinase Expression Increases Intracellular Sphingosine-1-Phosphate and Promotes Cell Growth and Survival
Ana Olivera,
Ana Olivera
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Takafumi Kohama,
Takafumi Kohama
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Lisa Edsall,
Lisa Edsall
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Victor Nava,
Victor Nava
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Olivier Cuvillier,
Olivier Cuvillier
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Samantha Poulton,
Samantha Poulton
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Sarah Spiegel
Sarah Spiegel
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
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Ana Olivera
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Takafumi Kohama
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Lisa Edsall
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Victor Nava
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Olivier Cuvillier
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Samantha Poulton
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
Sarah Spiegel
aDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007
1.used in this paper: Ac-DEVD-AMC, acetyl-Asp-Glu-Val-Asp-aminomethylcoumarin; BrdU, bromodeoxyuridine; DMS, N,N-dimethylsphingosine; EDG, endothelial differentiation gene; GFP, green fluorescent protein; GPCR, G protein coupled receptors; SPHK, sphingosine kinase; SPP, sphingosine-1-phosphate; TNF, tumor necrosis factor
Received:
February 02 1999
Revision Requested:
September 20 1999
Accepted:
September 22 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Cell Biol (1999) 147 (3): 545–558.
Article history
Received:
February 02 1999
Revision Requested:
September 20 1999
Accepted:
September 22 1999
Citation
Ana Olivera, Takafumi Kohama, Lisa Edsall, Victor Nava, Olivier Cuvillier, Samantha Poulton, Sarah Spiegel; Sphingosine Kinase Expression Increases Intracellular Sphingosine-1-Phosphate and Promotes Cell Growth and Survival. J Cell Biol 1 November 1999; 147 (3): 545–558. doi: https://doi.org/10.1083/jcb.147.3.545
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