Mitochondria and cell death: outer membrane permeabilization and beyond

被引:1967
作者
Tait, Stephen W. G. [1 ]
Green, Douglas R. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
关键词
CYTOCHROME-C RELEASE; CASPASE ACTIVATION; NUCLEOTIDE EXCHANGE; CYCLOPHILIN-D; DIFFERENTIAL REQUIREMENT; NEGATIVE REGULATION; APOPTOTIC PROTEINS; INHIBITS APOPTOSIS; BAK ACTIVATION; ENDONUCLEASE-G;
D O I
10.1038/nrm2952
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial outer membrane permeabilization (MOMP) is often required for activation of the caspase proteases that cause apoptotic cell death. Various intermembrane space (IMS) proteins, such as cytochrome c, promote caspase activation following their mitochondrial release. As a consequence, mitochondrial outer membrane integrity is highly controlled, primarily through interactions between pro-and anti-apoptotic members of the B cell lymphoma 2 (BCL-2) protein family. Following MOMP by pro-apoptotic BCL-2-associated X protein (BAX) or BCL-2 antagonist or killer (BAK), additional regulatory mechanisms govern the mitochondrial release of IMS proteins and caspase activity. MOMP typically leads to cell death irrespective of caspase activity by causing a progressive decline in mitochondrial function, although cells can survive this under certain circumstances, which may have pathophysiological consequences.
引用
收藏
页码:621 / 632
页数:12
相关论文
共 151 条
  • [1] Mitochondrial disruption in Drosophila apoptosis
    Abdelwahid, Eltyeb
    Yokokura, Takakazu
    Krieser, Ronald J.
    Balasundaram, Sujatha
    Fowle, William H.
    White, Kristin
    [J]. DEVELOPMENTAL CELL, 2007, 12 (05) : 793 - 806
  • [2] A cytochrome c mutant with high electron transfer and antioxidant activities but devoid of apoptogenic effect
    Abdullaev, ZK
    Bodrova, ME
    Chernyak, BV
    Dolgikh, DA
    Kluck, RM
    Perverzev, MO
    Arseniev, AS
    Efremov, RG
    Kirpichnikov, MP
    Mokhova, EN
    Newmeyer, DD
    Roder, H
    Skulachev, VP
    [J]. BIOCHEMICAL JOURNAL, 2002, 362 : 749 - 754
  • [3] Inhibition of caspase-9 through phosphorylation at Thr 125 by ERK MAPK
    Allan, LA
    Morrice, N
    Brady, S
    Magee, G
    Pathak, S
    Clarke, PR
    [J]. NATURE CELL BIOLOGY, 2003, 5 (07) : 647 - U45
  • [4] Phosphorylation of caspase-9 by CDK1/cyclin B1 protects mitotic cells against apoptosis
    Allan, Lindsey A.
    Clarke, Paul R.
    [J]. MOLECULAR CELL, 2007, 26 (02) : 301 - 310
  • [5] Apoptosis and autophagy: Regulation of caspase-9 by phosphorylation
    Allan, Lindsey A.
    Clarke, Paul R.
    [J]. FEBS JOURNAL, 2009, 276 (21) : 6063 - 6073
  • [6] Inhibition of Bax channel-forming activity by Bcl-2
    Antonsson, B
    Conti, F
    Ciavatta, A
    Montessuit, S
    Lewis, S
    Martinou, I
    Bernasconi, L
    Bernard, A
    Mermod, JJ
    Mazzei, G
    Maundrell, K
    Gambale, F
    Sadoul, R
    Martinou, JC
    [J]. SCIENCE, 1997, 277 (5324) : 370 - 372
  • [7] Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation
    Arnoult, D
    Grodet, A
    Lee, YJ
    Estaquier, J
    Blackstone, C
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (42) : 35742 - 35750
  • [8] Mitochondrial release of AIF and EndoG requires caspase activation downstream of Bax/Bak-mediated permeabilization
    Arnoult, D
    Gaume, B
    Karbowski, M
    Sharpe, JC
    Cecconi, F
    Youle, RJ
    [J]. EMBO JOURNAL, 2003, 22 (17) : 4385 - 4399
  • [9] Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death
    Baines, Christopher P.
    Kaiser, Robert A.
    Sheiko, Tatiana
    Craigen, William J.
    Molkentin, Jeffery D.
    [J]. NATURE CELL BIOLOGY, 2007, 9 (05) : 550 - U122
  • [10] Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death
    Baines, CP
    Kaiser, RA
    Purcell, NH
    Blair, NS
    Osinska, H
    Hambleton, MA
    Brunskill, EW
    Sayen, MR
    Gottlieb, RA
    Dorn, GW
    Robbins, J
    Molkentin, JD
    [J]. NATURE, 2005, 434 (7033) : 658 - 662