Sphingosine-1-phosphate induces apoptosis of cultured hippocampal neurons that requires protein phosphatases and activator protein-1 complexes

• Published in: Neuroscience Vol. 94; no. 2; pp. 405 - 415
• Main Authors: Moore, A.N, Kampfl, A.W, Zhao, X, Hayes, R.L, Dash, P.K
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.01.1999
• Subjects: Animals; AP-1 complexes; Apoptosis - drug effects; Base Sequence; c-Fos; calcineurin; caspase; Cells, Cultured; Fetus; Genes, fos - drug effects; Genes, jun - drug effects; Hippocampus - cytology; Hippocampus - enzymology; Kinetics; Lysophospholipids; Neurons - cytology; Neurons - drug effects; Neurons - enzymology; Oligodeoxyribonucleotides - pharmacology; Oligodeoxyribonucleotides, Antisense - pharmacology; phosphatases; Phosphoprotein Phosphatases - metabolism; Protein Phosphatase 2; Rats; Regulatory Sequences, Nucleic Acid; Sphingosine - analogs & derivatives; Sphingosine - pharmacology; sphingosine-1-phosphate; Tetradecanoylphorbol Acetate - pharmacology; Transcription Factor AP-1 - metabolism; TRE sequence; AP-1 complexes; IP 3, inositol 1,4,5-trisphosphate; AP-1, activator protein-1; EDTA, ethylenediaminetetra-acetate; HEPES, N-2-hydroxyethylpiperazine- N′-2-ethanesulfonic acid; LDH, lactate dehydrogenase; c-Fos; PP, protein phosphatase; ATA, aurintricarboxylic acid; calcineurin; TRE sequence; caspase; PBS, phosphate-buffered saline; BAPTA-AM, 1,2-bis-(2-aminophenoxy)ethane- N, N, N′, N′-tetra-acetate acetoxymethyl ester; SPP, sphingosine-1-phosphate; TRE, phorbol-12-myristate-13-acetate response element; EGTA, ethyleneglycolbis(aminoethyl ether)tetra-acetate; EMSA, electrophoretic mobility shift assay; phosphatases; MAPK, mitogen-activated protein kinase
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/S0306-4522(99)00288-2

In this study, we report that mobilization of internal Ca 2+ by sphingosine-1-phosphate, a metabolite of ceramide, induces apoptosis in cultured hippocampal neurons. This sphingosine-1-phosphate-induced apoptosis is dependent upon the activation of protein phosphatases, possibly calcineurin and phosphatase 2A (or a related phosphatase). In addition, pretreatment of neurons with double-stranded oligonucleotides containing the metallothionein phorbol-12-myristate-13-acetate response element sequence as transcription factor decoys suppressed apoptosis. In contrast, double-stranded oligonucleotides containing either the c-jun or SV40 phorbol-12-myristate-13-acetate response element sequences were ineffective. Electrophoretic mobility shift assays and supershift assays revealed that c-Fos-containing activator protein-1 complexes preferentially bound the metallothionein phorbol-12-myristate-13-acetate response element sequence-containing oligonucleotides. Furthermore, antisense oligonucleotides to c-fos and c-jun were also protective. The apoptotic death of hippocampal neurons has been hypothesized to contribute to the cognitive impairments observed following insults to the brain. While increases in intracellular calcium are thought to be key mediators of neuronal apoptosis, the biochemical cascade(s) activated as a result of increased Ca 2+ which mediates apoptosis of hippocampal neurons is (are) not well understood. The findings presented in this study suggest that mobilization of internal calcium via prolonged exposure of sphingosine-1-phosphate induces apoptosis of hippocampal neurons in culture. Sustained increases in intracellular calcium activate a phosphatase cascade that includes calcineurin and a phosphatase 2A-like phosphatase, and leads to the expression of genes containing metallothionein phorbol-12-myristate-13-acetate response element (TGAGTCA)-type enhancer sequences. The expression of genes containing TGAGTCA-type enhancer sequences appears to be essential for sphingosine-1-phosphate-induced apoptosis of hippocampal neurons.