Vol. 59, Issue 5, 1249-1255, May 2001

Synthetic Phytoceramides Induce Apoptosis with Higher Potency than Ceramides

Onyou Hwang, Guncheol Kim, Yeon Joo Jang, Seong Who Kim, Guiyong Choi, Hyun Jin Choi, Seon Young Jeon, Don Gyu Lee, and Jae Dam Lee

Department of Biochemistry, University of Ulsan College of Medicine, Seoul, Korea (O.H., Y.J.J., S.W.K., H.J.C., J.D.L.); Department of Chemistry, College of Natural Sciences, Chungnam National University, Taejon, Korea (G.K., S.Y.J., D.G.L.); and The SphingoBiolipid Corp, Yongin, Korea (G.C.)

Ceramides are naturally occurring compounds recognized to mediate apoptosis. N-acylsphingosines, containing a double bond at carbons 4 and 5 of their sphingoid backbone, are thought to be the active form, because N-acylsphinganines with completely saturated sphingoid are inactive. In the present study, we synthesized a series of N-acyl-4D-ribo-phytosphingosines (phytoceramides) that contain a hydroxyl group at carbon 4 and investigated structure-cytotoxicity relationship of the presumed functional groups in ceramides. N-Acetylphytoceramide (PCer2) and N-hexanoylphytoceramide (PCer6) were found to be more cytotoxic than ceramides as determined by released lactate dehydrogenase activity and morphological criteria. This was not caused by intracellular conversion of phytoceramides to ceramides, because no N-hexanoylsphingosine was formed after incubation of cell lysate with PCer6. Among phytoceramides having acyl chains two to eight carbons long, the cytotoxicity was highest with five or six carbons. The carbonyl group of the amide bond did not seem to be critical, because substitution of the oxygen with sulfur did not influence the cytotoxicity. The phytoceramide-induced cell death was observed to be apoptotic in nature with the use of terminal deoxynucleotidyl transferase dUTP nick-end labeling and propidium iodide staining. Because phytoceramides can be readily synthesized from yeast sources, they may present a potential and economical alternative to ceramide in future studies and therapies.