Role for ceramide as an endogenous mediator of Fas-induced cytotoxicity.

CG Tepper, S Jayadev, BIN LIu… - Proceedings of the …, 1995 - National Acad Sciences
CG Tepper, S Jayadev, BIN LIu, A Bielawska, R Wolff, S Yonehara, YA Hannun, MF Seldin
Proceedings of the National Academy of Sciences, 1995National Acad Sciences
Triggering of the Fas/APO-1 cell-surface receptor induces apoptosis through an
uncharacterized chain of events. Exposure of Fas-sensitive cells to an agonist monoclonal
antibody induced cell death and a 200-300% elevation in endogenous levels of the
sphingolipid ceramide, a proposed intracellular mediator of apoptosis. In contrast, similar
treatment of Fas-resistant cells caused insignificant changes in ceramide levels. Because
resistant cell lines expressed the Fas antigen, these results indicate that these cells have a …
Triggering of the Fas/APO-1 cell-surface receptor induces apoptosis through an uncharacterized chain of events. Exposure of Fas-sensitive cells to an agonist monoclonal antibody induced cell death and a 200-300% elevation in endogenous levels of the sphingolipid ceramide, a proposed intracellular mediator of apoptosis. In contrast, similar treatment of Fas-resistant cells caused insignificant changes in ceramide levels. Because resistant cell lines expressed the Fas antigen, these results indicate that these cells have a defect in the proximal signaling events leading to ceramide generation. Exposure of the resistant cell lines to a synthetic analog of ceramide induced apoptosis, thus bypassing Fas resistance and indicating that the signaling pathways downstream of ceramide were intact. Furthermore, activation of protein kinase C with the diacylglycerol analog phorbol 12-myristate 13-acetate significantly reduced Fas-induced cytotoxicity, suggesting opposing roles for ceramide and protein kinase C in regulation of apoptosis. These results provide evidence for ceramide as a necessary and sufficient lipid mediator of Fas-mediated apoptosis and suggest this process may be modulated via activation of additional signal-transduction pathways.
National Acad Sciences