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Sphingosine kinases, sphingosine 1-phosphate, apoptosis and diseases

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Volume 1758, Issue 12, Pages 2016-2026

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbamem.2006.08.007

Keywords

sphingosine kinase; sphingosine-1-phosphate; apoptosis; cancer; allergy; asthma; development

Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [CA61774] Funding Source: Medline
  3. NIAID NIH HHS [AI50094] Funding Source: Medline
  4. NIGMS NIH HHS [GM43880] Funding Source: Medline

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Sphingolipids are ubiquitous components of cell membranes and their metabolites ceramide (Cer), sphingosine (Sph), and sphingosine-1-phosphate (S I P) have important physiological functions, including regulation of cell growth and survival. Cer and Sph are associated with growth arrest and apoptosis. Many stress stimuli increase levels of Cer and Sph, whereas suppression of apoptosis is associated with increased intracellular levels of S1P. In addition, extracellular/secreted S1P regulates cellular processes by binding to five specific G protein coupled-receptors (GPCRs). SIP is generated by phosphorylation of Sph catalyzed by two isoforms of sphingosine kinases (SphK), type I and type 2, which are critical regulators of the sphingolipid rheostat, producing pro-survival SIP and decreasing levels of pro-apoptotic Sph. Since sphingolipid metabolism is often dysregulated in many diseases, targeting SphKs is potentially clinically relevant. Here we review the growing recent literature on the regulation and the roles of SphKs and S I P in apoptosis and diseases. (c) 2006 Elsevier B.V. All rights reserved.

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