REVIEW: Roles of Sphingosine-1-phosphate in Cell Growth, Differentiation, and Death

S. Spiegel^*, O. Cuvillier, L. Edsall, T. Kohama, R. Menzeleev, A. Olivera, D. Thomas, Z. Tu, J. Van Brocklyn, and F. Wang

Department of Biochemistry and Molecular Biology, Georgetown University Medical Center, 357 Basic Science Building, 3900 Reservoir Road NW, Washington, DC 20007, USA; fax: (202) 687-0260; E-mail: spiegel@biochem1.basic-sci.georgetown.edu

^* To whom correspondence should be addressed.

Received August 18, 1997

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Recent evidence suggests that branching pathways of sphingolipid metabolism may mediate either apoptotic or mitogenic responses depending on the cell type and the nature of the stimulus. While ceramide has been shown to be an important regulatory component of apoptosis induced by tumor necrosis factor alpha and the Fas ligand, sphingosine-1-phosphate (SPP), a further metabolite of ceramide, has been implicated as a second messenger in cellular proliferation and survival induced by platelet-derived growth factor, neuronal growth factor, and serum. SPP protects cells from apoptosis resulting from elevations of ceramide. Inflammatory cytokines stimulate sphingomyelinase, but not ceramidase, leading to accumulation of ceramide, whereas growth signals also stimulate ceramidase and sphingosine kinase leading to increased SPP levels. We propose that the dynamic balance between levels of sphingolipid metabolites, ceramide, and SPP and consequent regulation of different members of the mitogen-activated protein kinases (JNK versus ERK) family is an important factor that determines whether a cell survives or dies.

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KEY WORDS: sphingosine-1-phosphate, apoptosis, cell growth, signal transduction

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