The PKC delta inhibitor, rottlerin, induces apoptosis of haematopoietic cell lines through mitochondrial membrane depolarization and caspases' cascade

被引:49
作者
Liao, YF
Hung, YC
Chang, WH
Tsay, GJ
Hour, TC
Hung, HC
Liu, GY
机构
[1] Chung Shan Med Univ, Inst Immunol, Taichung, Taiwan
[2] Natl Chung Hsing Univ, Dept Life Sci, Taichung 40227, Taiwan
[3] Chung Shan Med Univ, Sch Appl Chem, Taichung, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Internal Med, Taichung, Taiwan
[5] Kaohsiung Med Univ, Dept Biochem, Kaohsiung, Taiwan
关键词
Mallotus philippinensis; Euphorbiaceae; Rottlerin; apoptosis; mitochondrial membrane potential; cytochrome c; caspase;
D O I
10.1016/j.lfs.2005.01.010
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rottlerin is a widely selective protein kinase C delta (PKC delta) inhibitor isolated from Mallotus philippinensis. It shown to be effective against several human tumor cell lines and in potentiating chemotherapy-induced cytotoxcicity. Using the trypan blue exclusion assay, we demonstrated that rottlerin reduced the viability in a dose- and time-dependent manner of human leukemia HL60 cells, human acute T cell leukemia Jurkat cells and mouse macrophage RAW 264.7 cells. Rottlerin caused apoptosis and the apaptotic processing was inhibited by a caspase inhibitor, z-VAD-fmk, in these haematopoietic cells. The apoptosis-inducing activities were determined by nuclear condensation, sub-G, appearance, DNA fragmentation, loss of mitochondrial membrane potential release of mitochondrial cytochrome c into cytoplasm and proteolytic activation of caspase 9 and 3. Expression of PKC delta and Bcl-2 protein inhibited Delta psi(m) change and repressed cell death. These studies suggest that the cytotoxic effects of rottlerin through inhibition Of PKC delta cause mitochondrial dysfunction, cytochrome c release from mitochondria into cytoplasm and the activation of caspases' cascade. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:707 / 719
页数:13
相关论文
共 35 条
[1]   Apoptosomes: engines for caspase activation [J].
Adams, JM ;
Cory, S .
CURRENT OPINION IN CELL BIOLOGY, 2002, 14 (06) :715-720
[2]   Regulation of cell apoptosis by protein kinase c δ [J].
Brodie, C ;
Blumberg, PM .
APOPTOSIS, 2003, 8 (01) :19-27
[3]   Early mitochondrial activation and cytochrome c up-regulation during apoptosis [J].
Chandra, D ;
Liu, JW ;
Tang, DG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) :50842-50854
[4]   Effect of baicalein on apoptosis of the human Hep G2 cell line was induced by mitochondria dysfunction [J].
Chang, WH ;
Chen, CH ;
Gaul, RJ ;
Lin, CC ;
Tsai, CL ;
Tsai, K ;
Lu, FJ .
PLANTA MEDICA, 2002, 68 (04) :302-306
[5]  
Clark AS, 2003, CANCER RES, V63, P780
[6]   Specificity and mechanism of action of some commonly used protein kinase inhibitors [J].
Davies, SP ;
Reddy, H ;
Caivano, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2000, 351 (351) :95-105
[7]   Roles of mitochondria in health and disease [J].
Duchen, MR .
DIABETES, 2004, 53 :S96-S102
[8]   Apoptosis via the B cell antigen receptor requires Bax translocation and involves mitochondrial depolarization, cytochrome C release, and caspase-9 activation [J].
Eldering, E ;
Mackus, WJM ;
Derks, IAM ;
Evers, LM ;
Beuling, E ;
Teeling, P ;
Lens, SMA ;
van Oers, MHJ ;
van Lier, RAW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (07) :1950-1960
[9]   The pathophysiology of mitochondrial cell death [J].
Green, DR ;
Kroemer, G .
SCIENCE, 2004, 305 (5684) :626-629
[10]   THE MOUSE EAR EDEMA - A QUANTITATIVELY EVALUABLE ASSAY FOR TUMOR PROMOTING COMPOUNDS AND FOR INHIBITORS OF TUMOR PROMOTION [J].
GSCHWENDT, M ;
KITTSTEIN, W ;
FURSTENBERGER, G ;
MARKS, F .
CANCER LETTERS, 1984, 25 (02) :177-185