Cationic gradient reversal and cytoskeleton-independent volume regulatory pathways define an early stage of apoptosis

被引:63
作者
Bortner, Carl D. [1 ]
Sifre, Maria I. [1 ]
Cidlowski, John A. [1 ]
机构
[1] NIEHS, NIH, Dept Hlth & Human Serv, Lab Signal Transduct, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1074/jbc.M707809200
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
Cell shrinkage, or apoptotic volume decrease ( AVD), is a ubiquitous characteristic of programmed cell death that is independent of the death stimulus and occurs in all examples of apoptosis. Here we distinguished two specific stages of AVD based on cell size and a unique early reversal of intracellular ions that occurs in response to activation of both intrinsic and extrinsic cell death signal pathways. The primary stage of AVD is characterized by an early exchange of the normal intracellular ion distribution for sodium from 12 to 113.6 mM and potassium from 139.5 to 30 mM. This early ionic reversal is associated with a 20 - 40% decrease in cell volume, externalization of phosphatidylserine, loss of mitochondrial membrane potential, and caspase activation and activity along with nuclear condensation that occurs independent of actin cytoskeleton disruption. Disruption of the actin cytoskeleton, however, prevents a secondary stage of AVD in apoptotic cells, characterized by a loss of both potassium and sodium that results in an 80 - 85% loss in cell volume, DNA degradation, and apoptotic body formation. Together these studies demonstrate that AVD occurs in two distinct stages with the earliest stage reflecting a cellular cationic gradient reversal.
引用
收藏
页码:7219 / 7229
页数:11
相关论文
共 33 条
  • [1] INTRACELLULAR IONIC VARIATIONS IN THE APOPTOTIC DEATH OF L-CELLS BY INHIBITORS OF CELL-CYCLE PROGRESSION
    BARBIERO, G
    DURANTI, F
    BONELLI, G
    AMENTA, JS
    BACCINO, FM
    [J]. EXPERIMENTAL CELL RESEARCH, 1995, 217 (02) : 410 - 418
  • [2] Barros LF, 2002, BIOL RES, V35, P209
  • [3] Characterization of cell volume loss in CEM-C7A cells during dexamethasone-induced apoptosis
    Benson, RSP
    Heer, S
    Dive, C
    Watson, AJM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (04): : C1190 - C1203
  • [4] A necessary role for cell shrinkage in apoptosis
    Bortner, CD
    Cidlowski, JA
    [J]. BIOCHEMICAL PHARMACOLOGY, 1998, 56 (12) : 1549 - 1559
  • [5] The role of apoptotic volume decrease and ionic homeostasis in the activation and repression of apoptosis
    Bortner, CD
    Cidlowski, JA
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2004, 448 (03): : 313 - 318
  • [6] Uncoupling cell shrinkage from apoptosis reveals that Na+ influx is required for volume loss during programmed cell death
    Bortner, CD
    Cidlowski, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) : 39176 - 39184
  • [7] Cellular mechanisms for the repression of apoptosis
    Bortner, CD
    Cidlowski, JA
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2002, 42 : 259 - 281
  • [8] Plasma membrane depolarization without repolarization is an early molecular event in anti-Fas-induced apoptosis
    Bortner, CD
    Gómez-Angelats, M
    Cidlowski, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (06) : 4304 - 4314
  • [9] A primary role for K+ and Na+ efflux in the activation of apoptosis
    Bortner, CD
    Hughes, FM
    Cidlowski, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) : 32436 - 32442
  • [10] Physiological concentrations of K+ inhibit cytochrome c-dependent formation of the apoptosome
    Cain, K
    Langlais, C
    Sun, XM
    Brown, DG
    Cohen, GM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) : 41985 - 41990