Apoptotic activities of C2-ceramide and C2-dihydroceramide homologues against HL-60 cells

被引:33
作者
Shikata, K [1 ]
Niiro, H [1 ]
Azuma, H [1 ]
Ogino, K [1 ]
Tachibana, T [1 ]
机构
[1] Osaka City Univ, Grad Sch Engn, Dept Appl & Bioappl Chem, Sumiyoshi Ku, Osaka 5588585, Japan
关键词
D O I
10.1016/S0968-0896(03)00228-1
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
The apoptotic activities of non-natural ceramide homologues, C2-homo-ceramide, C2-homo-dihydroceramide, C2-bishomo-ceramide and C2-bishomo-dihydroceramide, were examined using human leukemia HL-60 cells. The apoptotic activity was in order of C2-ceramide > C2-homo-ceramideapproximate toC2-bishomo-ceramide and the activities of the L-erythro- and D-erythro-ceramide homologues were similar. The morphological features of the cells, DNA fragmentations, proteolytic processing of pro-caspase-3 and the cleavage of PARP as the result of treatments with these homologues indicated that cell death was induced by apoptosis. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2723 / 2728
页数:6
相关论文
共 29 条
[1]   Ceramide:: does it matter for T cells? [J].
Adam, D ;
Heinrich, M ;
Kabelitz, D ;
Schütze, S .
TRENDS IN IMMUNOLOGY, 2002, 23 (01) :1-4
[2]   Stereospecific total syntheses of sphingosine and its analogues from L-serine [J].
Azuma, H ;
Tamagaki, S ;
Ogino, K .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (11) :3538-3541
[3]  
BARNHOLZ Y, 1966, J BIOL CHEM, V241, P3731
[4]  
BIELAWSKA A, 1993, J BIOL CHEM, V268, P26226
[5]   The synthesis and biological characterization of a ceramide library [J].
Chang, YT ;
Choi, J ;
Ding, S ;
Prieschl, EE ;
Baumruker, T ;
Lee, JM ;
Chung, SK ;
Schultz, PG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (09) :1856-1857
[6]   Suppression of ceramide-mediated programmed cell death by sphingosine-1-phosphate [J].
Cuvillier, O ;
Pirianov, G ;
Kleuser, B ;
Vanek, PG ;
Coso, OA ;
Gutkind, JS ;
Spiegel, S .
NATURE, 1996, 381 (6585) :800-803
[7]   Sphingosine 1-phosphate inhibits activation of caspases that cleave poly(ADP-ribose) polymerase and lamins during Fas- and ceramide-mediated apoptosis in Jurkat T lymphocytes [J].
Cuvillier, O ;
Rosenthal, DS ;
Smulson, ME ;
Spiegel, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :2910-2916
[8]   TUMOR-NECROSIS-FACTOR-ALPHA ACTIVATES THE SPHINGOMYELIN SIGNAL TRANSDUCTION PATHWAY IN A CELL-FREE SYSTEM [J].
DRESSLER, KA ;
MATHIAS, S ;
KOLESNICK, RN .
SCIENCE, 1992, 255 (5052) :1715-1718
[9]   Use of sphingolipid analogs: benefits and risks [J].
Ghidoni, R ;
Sala, G ;
Giuliani, A .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1999, 1439 (01) :17-39
[10]   Synthesis of sphingomyelin carbon analogues as sphingomyelinase inhibitors [J].
Hakogi, T ;
Monden, Y ;
Taichi, M ;
Iwama, S ;
Fujii, S ;
Ikeda, K ;
Katsumura, S .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (14) :4839-4846