Pinocytic loading of cytochrome c into intact cells specifically induces caspase-dependent permeabilization of mitochondria:: evidence for a cytochrome c feedback loop

被引:17
作者
Gilmore, KJ [1 ]
Quinn, HE [1 ]
Wilson, MR [1 ]
机构
[1] Univ Wollongong, Dept Biol Sci, Wollongong, NSW 2522, Australia
关键词
cytochrome c; caspase activation; mitochondrial permeabilization;
D O I
10.1038/sj.cdd.4400858
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
Previous studies introduced cytochrome c into intact cells via the disruptive techniques of microinjection or electroporation to provide support for the hypothesis that, in whole cells, cytochrome c release from mitochondria triggers caspase activation and other degradative changes. However, the types of measurements that could be undertaken with these techniques was limited. We used the simple and relatively gentle technique of pinocytic loading to demonstrate that, in intact cells, cytosolic cytochrome c specifically induced activation of caspase-3- and -9-like enzymes, and a loss of mitochondrial polarization coincident with an increase in mitochondrial permeability, Our results support the prediction from in vitro studies that activation of caspases-3 and -9 is downstream of cytochrome c release and provide the first direct evidence that, in whole cells, cytochrome c-dependent caspase-activation can exert a feedback effect to elicit mitochondrial permeabilization and collapse of the mitochondrial trans-membrane potential.
引用
收藏
页码:631 / 639
页数:9
相关论文
共 40 条
  • [11] Gilmore K, 1999, CYTOMETRY, V36, P355, DOI 10.1002/(SICI)1097-0320(19990801)36:4<355::AID-CYTO11>3.0.CO
  • [12] 2-9
  • [13] Mitochondria and apoptosis
    Green, DR
    Reed, JC
    [J]. SCIENCE, 1998, 281 (5381) : 1309 - 1312
  • [14] Inhibition of mitochondrial respiratory chain complex I by TNF results in cytochrome c release, membrane permeability transition, and apoptosis
    Higuchi, M
    Proske, RJ
    Yeh, ETH
    [J]. ONCOGENE, 1998, 17 (19) : 2515 - 2524
  • [15] The release of cytochrome c from mitochondria: A primary site for Bcl-2 regulation of apoptosis
    Kluck, RM
    BossyWetzel, E
    Green, DR
    Newmeyer, DD
    [J]. SCIENCE, 1997, 275 (5303) : 1132 - 1136
  • [16] Cell-specific induction of apoptosis by microinjection of cytochrome c - Bcl-x(L) has activity independent of cytochrome c release
    Li, F
    Srinivasan, A
    Wang, Y
    Armstrong, RC
    Tomaselli, KJ
    Fritz, LC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (48) : 30299 - 30305
  • [17] Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis
    Li, HL
    Zhu, H
    Xu, CJ
    Yuan, JY
    [J]. CELL, 1998, 94 (04) : 491 - 501
  • [18] Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade
    Li, P
    Nijhawan, D
    Budihardjo, I
    Srinivasula, SM
    Ahmad, M
    Alnemri, ES
    Wang, XD
    [J]. CELL, 1997, 91 (04) : 479 - 489
  • [19] Induction of apoptotic program in cell-free extracts: Requirement for dATP and cytochrome c
    Liu, XS
    Kim, CN
    Yang, J
    Jemmerson, R
    Wang, XD
    [J]. CELL, 1996, 86 (01) : 147 - 157
  • [20] DFF, a heterodimeric protein that functions downstream of caspase-3 to trigger DNA fragmentation during apoptosis
    Liu, XS
    Zou, H
    Slaughter, C
    Wang, XD
    [J]. CELL, 1997, 89 (02) : 175 - 184