Adenovirus L4-100K assembly protein is a granzyme B substrate that potently inhibits granzyme B-mediated cell death

被引:67
作者
Andrade, F
Bull, HG
Thornberry, NA
Ketner, GW
Casciola-Rosen, LA
Rosen, A [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Cell Biol & Anat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21205 USA
[4] Merck Res Labs, Dept Biochem, Rahway, NJ 07065 USA
[5] Johns Hopkins Univ, Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
关键词
D O I
10.1016/S1074-7613(01)00149-2
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 lymphocytes kill virus-infected target cells and play a critical role in host recovery from viral infections. Granzyme B (GrB) is a cytotoxic lymphocyte granule protease that plays a critical role in mediating cytotoxicity. In these studies, we demonstrate that the adenovirus assembly protein L4-100K (100K) is a GrB substrate that prevents cytotoxic lymphocyte granule-induced apoptosis in infected target cells by potently inhibiting GrB. This inhibition is absolutely dependent on Asp-48 in 100K, found within a classic GrB consensus motif. 100K is the first viral protein described that exclusively targets the GrB pathway. It represents a novel class of viral protease inhibitor, in which an essential, multifunctional viral protein, which is vulnerable to specific proteolysis by GrB, expresses inhibitory function against that protease.
引用
收藏
页码:751 / 761
页数:11
相关论文
共 60 条
  • [1] ADENOVIRUS 5 DNA SEQUENCES PRESENT AND RNA SEQUENCES TRANSCRIBED IN TRANSFORMED HUMAN-EMBRYO KIDNEY-CELLS (HEK-AD-5 OR 293)
    AIELLO, L
    GUILFOYLE, R
    HUEBNER, K
    WEINMANN, R
    [J]. VIROLOGY, 1979, 94 (02) : 460 - 469
  • [2] Granzyme B directly and efficiently cleaves several downstream caspase substrates: Implications for CTL-induced apoptosis
    Andrade, F
    Roy, S
    Nicholson, D
    Thornberry, N
    Rosen, A
    Casciola-Rosen, L
    [J]. IMMUNITY, 1998, 8 (04) : 451 - 460
  • [3] Anel A, 1997, J IMMUNOL, V158, P1999
  • [4] Death receptors: Signaling and modulation
    Ashkenazi, A
    Dixit, VM
    [J]. SCIENCE, 1998, 281 (5381) : 1305 - 1308
  • [5] Granzyme B short-circuits the need for caspase 8 activity during granule-mediated cytotoxic T-lymphocyte killing by directly cleaving bid
    Barry, M
    Heibein, JA
    Pinkoski, MJ
    Lee, SF
    Moyer, RW
    Green, DR
    Bleackley, RC
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (11) : 3781 - 3794
  • [6] Granzyme A loading induces rapid cytolysis and a novel form of DNA damage independently of caspase activation
    Beresford, PJ
    Xia, ZN
    Greenberg, AH
    Lieberman, J
    [J]. IMMUNITY, 1999, 10 (05) : 585 - 594
  • [7] Bird P I, 1998, Results Probl Cell Differ, V24, P63
  • [8] Biochemical pathways of caspase activation during apoptosis
    Budihardjo, I
    Oliver, H
    Lutter, M
    Luo, X
    Wang, XD
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 : 269 - 290
  • [9] Cleavage by granzyme B is strongly predictive of autoantigen status: Implications for initiation of autoimmunity
    Casciola-Rosen, L
    Andrade, F
    Ulanet, D
    Wong, WB
    Rosen, A
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (06) : 815 - 825
  • [10] ASSEMBLY OF ADENOVIRUS MAJOR CAPSID PROTEIN IS MEDIATED BY A NONVIRION PROTEIN
    CEPKO, CL
    SHARP, PA
    [J]. CELL, 1982, 31 (02) : 407 - 415