Role of mitochondria and mitochondrial cytochrome c in tubeimoside I-mediated apoptosis of human cervical carcinoma HeLa cell line

被引:74
作者
Wang, F
Ma, RD [1 ]
Yu, LJ
机构
[1] Zhanjiang Ocean Univ, Guangdong Provincial Key Lab Marine Mat Med, Zhanjiang 524025, Guangdong, Peoples R China
[2] Chinese Acad Sci, S China Sea Inst Oceanol, Guangzhou 510301, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Guangzhou, Peoples R China
关键词
tubeimoside I; mitochondria; cytochrome c; apoptosis; HeLa cells;
D O I
10.1007/s00280-005-0047-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Tubeimoside I (TBMS1), a triterpenoid saponin, isolated from the tubers of Bolbostemma paniculatum, showed potent antitumor and antitumor-promoting effects. The objective of this study is to investigate the role of mitochondria and mitochondria cytochrome c in TBMS1-mediated apoptosis of human cervical carcinoma HeLa cell line. Methods: Viability of HeLa cells was measured by MTT assay. Apoptotic induction by TBMS1 was determined by fluorescence microscopy, flow cytometry and gel electrophoresis of fragmented DNA. Mitochondrial transmembrane potential (triangle psi m) was assayed by flow cytometry. Cytochrome c (Cyt c) was detected by Western blotting. Results: The results showed that Cyclosporin A (CsA) partly protected HeLa cells from growth inhibitory effect of TBMS1, and partly countered the ability of TBMS1 to rapidly induce apoptosis in HeLa cells, and that TBMS1 decreased triangle psi m and induced Cyt c release by a mechanism inhibited by CsA, and that TBMS1 induced apoptosis of HeLa cells dose-dependently in accordance with increase of cytosolic Cyt c. Conclusions: TBMS1 opens the permeability transition (PT) pore, thereby decreasing triangle psi m, releasing Cyt c from mitochondria, and further causing a series of events consistent with established mechanistic models of apoptosis.
引用
收藏
页码:389 / 399
页数:11
相关论文
共 47 条
[1]
Bedner E, 1999, CYTOMETRY, V36, P77, DOI 10.1002/(SICI)1097-0320(19990501)36:1<77::AID-CYTO10>3.3.CO
[2]
2-6
[3]
Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVD-specific caspase activation and independently of mitochondrial transmembrane depolarization [J].
Bossy-Wetzel, E ;
Newmeyer, DD ;
Green, DR .
EMBO JOURNAL, 1998, 17 (01) :37-49
[4]
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
[5]
Chiganças V, 2000, CANCER RES, V60, P2458
[6]
Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition [J].
Du, CY ;
Fang, M ;
Li, YC ;
Li, L ;
Wang, XD .
CELL, 2000, 102 (01) :33-42
[7]
[方敏 Fang Min], 2002, [北京大学学报. 医学版, Journal of peking university], V34, P1
[8]
Cyclosporin A, but not FK 506, protects mitochondria and neurons against hypoglycemic damage and implicates the mitochondrial permeability transition in cell death [J].
Friberg, H ;
Ferrand-Drake, M ;
Bengtsson, F ;
Halestrap, AP ;
Wieloch, T .
JOURNAL OF NEUROSCIENCE, 1998, 18 (14) :5151-5159
[9]
Gastman BR, 2000, CANCER RES, V60, P6811
[10]
The coordinate release of cytochrome c during apoptosis is rapid, complete and kinetically invariant [J].
Goldstein, JC ;
Waterhouse, NJ ;
Juin, P ;
Evan, GI ;
Green, DR .
NATURE CELL BIOLOGY, 2000, 2 (03) :156-162