Inhibition of sphingolipid induced apoptosis by caspase inhibitors indicates that sphingosine acts in an earlier part of the apoptotic pathway than ceramide

被引:87
作者
Sweeney, EA
Inokuchi, J
Igarashi, Y
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[2] Seikagaku Corp, Tokyo Res Inst, Tokyo, Japan
关键词
apoptosis; caspase; sphingosine; N; N-dimethylsphingosine; ceramide;
D O I
10.1016/S0014-5793(98)00198-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspases are specific proteases involved in apoptosis, and their inhibition by specific peptide inhibitors can inhibit apoptosis, With these inhibitors we examined the relationship of caspases and sphingolipids involved in the induction of apoptosis of human leukemic HL60 cells, We have previously shown that sphingosine (Sph) and its methylated derivative dimethylsphingosine (DMS) effectively induce apoptosis in HL60 cells, Using these lipids as ell as ceramide analogues we found both similarities and differences in the caspase involvement in apoptosis induced by the two distinct lipid types, The wide-spectrum caspase inhibitor Z-VAD-FMK and Z-DEVD-FMX, an inhibitor of the downstream caspases 3 (CPP32, Yama) and 7, both inhibited apoptosis induced by all the lipids tested, Z-AAD-FMK which inhibits the serine protease Granzyme B, inhibited Sph/DMS induced apoptosis, but little or no effect on ceramide induced apoptosis, Granzyme B shares a substrate sequence preference with upstream caspases capable of activating themselves and other caspases downstream, Z-IETD-FMK, which inhibits caspase 8/FLICE also inhibited Sph/DMS induced apoptosis with no inhibition of apoptosis induced by either ceramide, Together, these data indicate that Sph/DMS act independently from ceramide in the apoptosis pathway and further suggest that Sph/DMS act earlier in the pathway than ceramide and are involved upstream of even the early proteases, whereas the point of action for ceramide is downstream of the early proteases but upstream from the late caspases. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:61 / 65
页数:5
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