Proteases and cell-mediated cytotoxicity

被引:24
作者
Darmon, AJ
Bleackley, RC
机构
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[2] Ludwig Inst Canc Res, London W1P 8BT, England
关键词
apoptosis; granzymes; death receptors; ICE/Ced-3; proteases; caspases;
D O I
10.1615/CritRevImmunol.v18.i3.50
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytotoxic T lymphocytes and natural killer cells represent the body's primary defense against viral-infected and tumorigenic cells. The classically described mechanism by which these cells induce target cell death is granule mediated: cytolytic granules within the killer cell are directionally exocytozed toward the target cell, and the granule contents inflict a "lethal hit" on the target cell. A second mechanism of cytotoxicity is now known to exist, and utilizes cell surface receptors on the target cell, for which the ligand is expressed on the killer cell. Receptor oligomerization results in the recruitment of cytoplasmic proteins to the receptors and the transduction of a death signal to the target cell. In both granule-and receptor-mediated cytotoxicity, the target cell dies through a defined series of steps, which together are termed apoptosis. Recent work on apoptosis has defined a family of cysteine proteases, the caspases, which appear to be involved in the initiation of apoptosis in response to a number of stimuli. This review focuses on studies that link these proteases to target cell death induced by cytotoxic cells.
引用
收藏
页码:255 / 273
页数:19
相关论文
共 181 条
  • [1] Ahmad M, 1997, CANCER RES, V57, P615
  • [2] Involvement of caspase-1 and caspase-3 in the production and processing of mature human interleukin 18 in monocytic THP.1 cells
    Akita, K
    Ohtsuki, T
    Nukada, Y
    Tanimoto, T
    Namba, M
    Okura, T
    TakakuraYamamoto, R
    Torigoe, K
    Gu, Y
    Su, MSS
    Fujii, M
    SatohItoh, M
    Yamamoto, K
    Kohno, K
    Ikeda, M
    Kurimoto, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) : 26595 - 26603
  • [3] Human ICE/CED-3 protease nomenclature
    Alnemri, ES
    Livingston, DJ
    Nicholson, DW
    Salvesen, G
    Thornberry, NA
    Wong, WW
    Yuan, JY
    [J]. CELL, 1996, 87 (02) : 171 - 171
  • [4] Anel A, 1997, J IMMUNOL, V158, P1999
  • [5] Mechanisms of lysis by cytotoxic T cells
    Atkinson, EA
    Bleackley, RC
    [J]. CRITICAL REVIEWS IN IMMUNOLOGY, 1995, 15 (3-4) : 359 - 384
  • [6] BING A, 1996, CANCER RES, V56, P438
  • [7] TRAMP, a novel apoptosis-mediating receptor with sequence homology to tumor necrosis factor receptor 1 and Fas(Apo-1/CD95)
    Bodmer, JL
    Burns, K
    Schneider, P
    Hofmann, K
    Steiner, V
    Thome, M
    Bornand, T
    Hahne, M
    Schroter, M
    Becker, K
    Wilson, A
    French, LE
    Browning, JL
    MacDonald, HR
    Tschopp, J
    [J]. IMMUNITY, 1997, 6 (01) : 79 - 88
  • [8] A NOVEL PROTEIN THAT INTERACTS WITH THE DEATH DOMAIN OF FAS/APO1 CONTAINS A SEQUENCE MOTIF RELATED TO THE DEATH DOMAIN
    BOLDIN, MP
    VARFOLOMEEV, EE
    PANCER, Z
    METT, IL
    CAMONIS, JH
    WALLACH, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) : 7795 - 7798
  • [9] Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death
    Boldin, MP
    Goncharov, TM
    Goltsev, YV
    Wallach, D
    [J]. CELL, 1996, 85 (06) : 803 - 815
  • [10] MICROFILAMENT REORGANIZATION DURING APOPTOSIS - THE ROLE OF GAS2, A POSSIBLE SUBSTRATE FOR ICE-LIKE PROTEASES
    BRANCOLINI, C
    BENEDETTI, M
    SCHNEIDER, C
    [J]. EMBO JOURNAL, 1995, 14 (21) : 5179 - 5190