Hsu S C, Wu C C, Luh T Y, Chou C K, Han S H, Lai M Z
Graduate Institute of Microbiology, National Taiwan University School of Medicine, Taiwan, China.
Blood. 1998 Apr 15;91(8):2658-63.
Ceramide has been suggested as the secondary messenger mediating the apoptotic signal for Fas engagement. By using different inhibitors, we demonstrated here that ceramide is unlikely a mediator of Fas-initiated apoptosis. First, cAMP prevented cell death induced by ceramide but not by Fas. Second, ceramide-triggered, but not Fas-triggered, apoptosis was antagonized by the free radical scavenger C60. Third, the metal chelator pyrrolidinedithiocarbamate suppressed ceramide-initiated DNA fragmentation but had no effect on the Fas-induced cell death. Fourth, the SAPK/ERK kinase dominant negative mutant, which attenuated ceramide-induced cell death, did not prevent Fas-induced apoptosis. Finally, activation of NF-kappaB inhibited ceramide-induced but not Fas-initiated apoptosis. The fact that many antagonists of ceramide-induced apoptosis could not suppress Fas-mediated cell death clearly indicates that ceramide is not the mediator for Fas-initiated apoptotic signal.
神经酰胺被认为是介导Fas激活凋亡信号的第二信使。通过使用不同的抑制剂,我们在此证明神经酰胺不太可能是Fas启动的细胞凋亡的介质。首先,cAMP可防止神经酰胺诱导的细胞死亡,但不能防止Fas诱导的细胞死亡。其次,自由基清除剂C60可拮抗神经酰胺触发的而非Fas触发的细胞凋亡。第三,金属螯合剂吡咯烷二硫代氨基甲酸盐可抑制神经酰胺引发的DNA片段化,但对Fas诱导的细胞死亡没有影响。第四,可减弱神经酰胺诱导的细胞死亡的SAPK/ERK激酶显性负性突变体不能阻止Fas诱导的细胞凋亡。最后,NF-κB的激活可抑制神经酰胺诱导的而非Fas启动的细胞凋亡。许多神经酰胺诱导的细胞凋亡拮抗剂不能抑制Fas介导的细胞死亡这一事实清楚地表明,神经酰胺不是Fas启动的凋亡信号的介质。