A role for actin in regulating apoptosis/programmed cell death: evidence spanning yeast, plants and animals

被引:165
作者
Franklin-Tong, Vernonica E. [2 ]
Gourlay, Campbell W. [1 ]
机构
[1] Univ Kent, Dept Biosci, Canterbury CT2 7NJ, Kent, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
actin; apoptosis; mitochondrion; programmed cell death (PCD); reactive oxygen species (ROS);
D O I
10.1042/BJ20080320
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
Achieving an understanding of how apoptosis/PCD (programmed cell death) is integrated within cellular responses to environmental and intracellular signals is a daunting task. From the sensation of a stimulus to the point of no return, a programme of cell death must engage specific pro-death components, whose effects can in turn be enhanced or repressed by downstream regulatory factors. In recent years, considerable progress has been made in our understanding of how components involved in these processes function. We now know that some of the factors involved in PCD networks have ancient origins that pre-date multicellularity and, indeed, eukaryotes themselves. A subject attracting much attention is the role that the actin cytoskeleton, itself a cellular component with ancient origins, plays in cell death regulation. Actin, a key cellular component, has an established role as a cellular sensor, with reorganization and alterations in actin dynamics being a well known consequence of signalling. A range of studies have revealed that actin also plays a key role in apoptosis/PCD regulation. Evidence implicating actin as a regulator of eukaryotic cell death has emerged from studies from the Animal, Plant and Fungal Kingdoms. Here we review recent data that provide evidence for an active, functional role for actin in determining whether PCD is triggered and executed, and discuss these findings within the context of regulation of actin dynamics.
引用
收藏
页码:389 / 404
页数:16
相关论文
共 227 条
  • [1] Molecular ordering of the initial signaling events of CD95
    Algeciras-Schimnich, A
    Shen, L
    Barnhart, BC
    Murmann, AE
    Burkhardt, JK
    Peter, ME
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (01) : 207 - 220
  • [2] Actin dependent CD95 internalization is specific for Type I cells
    Algeciras-Schimnich, A
    Peter, ME
    [J]. FEBS LETTERS, 2003, 546 (2-3) : 185 - 188
  • [3] On the origin, evolution, and nature of programmed cell death: a timeline of four billion years
    Ameisen, JC
    [J]. CELL DEATH AND DIFFERENTIATION, 2002, 9 (04) : 367 - 393
  • [4] ADF/cofilin mediates actin cytoskeletal alterations in LLC-PK cells during ATP depletion
    Ashworth, SL
    Southgate, EL
    Sandoval, RM
    Meberg, PJ
    Bamburg, JR
    Molitoris, BA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2003, 284 (04) : F852 - F862
  • [5] Mechanism of actin polymerization in cellular ATP depletion
    Atkinson, SJ
    Hosford, MA
    Molitoris, BA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (07) : 5194 - 5199
  • [6] Gelsolin in complex with phosphatidylinositol 4,5-bisphosphate inhibits caspase-3 and-9 to retard apoptotic progression
    Azuma, T
    Koths, K
    Flanagan, L
    Kwiatkowski, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (06) : 3761 - 3766
  • [7] A role for F-Actin in hexokinase-mediated glucose signaling1[C][W][OA]
    Balasubramanian, Rajagopal
    Karve, Abhijit
    Kandasamy, Muthugapatti
    Meagher, Richard B.
    Moore, Brandon D.
    [J]. PLANT PHYSIOLOGY, 2007, 145 (04) : 1423 - 1434
  • [8] Coordinated regulation of actin filament turnover by a high-molecular-weight Srv2/CAP complex, cofilin, profilin, and Aip1
    Balcer, HI
    Goodman, AL
    Rodal, AA
    Smith, E
    Kugler, J
    Heuser, JE
    Goode, BL
    [J]. CURRENT BIOLOGY, 2003, 13 (24) : 2159 - 2169
  • [9] ADF/cofilin and actin dynamics in disease
    Bamburg, JR
    Wiggan, OP
    [J]. TRENDS IN CELL BIOLOGY, 2002, 12 (12) : 598 - 605
  • [10] The downregulation of the pro-apoptotic protein Par-4 is critical for Ras-induced survival and tumor progression
    Barradas, M
    Monjas, A
    Diaz-Meco, MT
    Serrano, M
    Moscat, J
    [J]. EMBO JOURNAL, 1999, 18 (22) : 6362 - 6369