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Ceramide-1-phosphate promotes cell survival through activation of the phosphatidylinositol 3-kinase/protein kinase B pathway
Authors:Gómez-Muñoz Antonio  Kong Jennifer Y  Parhar Kuljit  Wang Shih Wei  Gangoiti Patricia  González Mónica  Eivemark Sharlene  Salh Bill  Duronio Vincent  Steinbrecher Urs P
Affiliation:Department of Biochemistry and Molecular Biology, Faculty of Sciences, University of the Basque Country, P.O. Box 644, 48080 Bilbao, Spain. gbpgomua@lg.ehu.es
Abstract:In this report, we show for the first time that ceramide-1-phosphate (C1P) stimulates the phosphatidylinositol 3-kinase (PI3-K)/protein kinase B (PKB) pathway, which is a major mechanism whereby growth factors promote cell survival. Also, C1P induced IkappaB phosphorylation, and enhanced the DNA binding activity of the transcription factor NF-kappaB. Apoptotic macrophages showed a marked reduction of Bcl-X(L) levels, and this was prevented by C1P. These findings suggest that C1P blocks apoptosis, at least in part, by stimulating the PI3-K/PKB/NF-kappaB pathway and maintaining the production of antiapoptotic Bcl-X(L). Based on these and our previous observations, we propose a working model for C1P in which inhibition of acid sphingomyelinase and the subsequent decrease in ceramide levels would allow cell signaling through stimulation of the PI3-K/PKB pathway to promote cell survival.
Keywords:A-SMase, acid sphingomyelinase   BMDM, bone marrow-derived macrophages   C1P, ceramide-1-phosphate   C2-, acetyl   C8-, octanoyl   CAPE, caffeic acid phenylethyl ester   EMSA, electromobility shift assay   FBS, fetal bovine serum   GAPDH, glyceraldehyde-3-phosphate dehydrogenase   M-CSF, macrophage colony stimulating factor   MAPK, mitogen-activated protein kinase   ERK, extracellular regulated kinase   MEK, MAPK/ERK kinase   MTS, [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt]   PI, phosphatidylinositol   PI3-K, phosphatidylinositol 3-kinase   PI (3,4,5) P3, phosphatidylinositol (3,4,5) trisphosphate   PKB, protein kinase B   PLD, phospholipase D   cPLA2, calcium-dependent cytosolic phospholipase A2   PMS, phenazine methosulfate   PTX, pertussis toxin   S1P, sphingosine-1-phosphate   TBS, Tris-buffered saline   TLC, thin-layer chromatography
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