TRAIL-R2: A novel apoptosis-mediating receptor for TRAIL

被引:991
作者
Walczak, H
DegliEsposti, MA
Johnson, RS
Smolak, PJ
Waugh, JY
Boiani, N
Timour, MS
Gerhart, MJ
Schooley, KA
Smith, CA
Goodwin, RG
Rauch, CT
机构
[1] Immunex Corporation, Seattle, WA 98101
关键词
apoptosis; caspases; FADD; TNF receptor family; TRAIL;
D O I
10.1093/emboj/16.17.5386
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
TRAIL is a member of the tumor necrosis factor (TNF) family of cytokines and induces apoptosis in a wide variety of cells. Based on homology searching of a private database, a receptor for TRAIL (DR4 or TRAIL-R1) was recently identified, Here we report the identification of a distinct receptor for TRAIL, TRAIL-R2, by ligand-based affinity purification and subsequent molecular cloning, TRAIL-R2 was purified independently as the only receptor for TRAIL detectable on the surface of two different human cell lines that undergo apoptosis upon stimulation with TRAIL. TRAIL-R2 contains two extracellular cysteine-rich repeats, typical for TNF receptor (TNFR) family members, and a cytoplasmic death domain. TRAIL binds to recombinant cell-surface-expressed TRAIL-R2, and TRAIL-induced apoptosis is inhibited by a TRAIL-R2-Fc fusion protein. TRAIL-R2 mRNA is widely expressed and the gene encoding TRAIL-R2 is located on human chromosome 8p22-21. Like TRAIL-R1, TRAIL-R2 engages a caspase-dependent apoptotic pathway but, in contrast to TRAIL-R1, TRAIL-R2 mediates apoptosis via the intracellular adaptor molecule FADD/MORT1. The existence of two distinct receptors for the same ligand suggests an unexpected complexity to TRAIL biology, reminiscent of dual receptors for TNF, the canonical member of this family.
引用
收藏
页码:5386 / 5397
页数:12
相关论文
共 64 条
  • [1] FAS LIGAND MEDIATES ACTIVATION-INDUCED CELL-DEATH IN HUMAN T-LYMPHOCYTES
    ALDERSON, MR
    TOUGH, TW
    DAVISSMITH, T
    BRADDY, S
    FALK, B
    SCHOOLEY, KA
    GOODWIN, RG
    SMITH, CA
    RAMSDELL, F
    LYNCH, DH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) : 71 - 77
  • [2] FROM AIDS TO PARASITE INFECTION - PATHOGEN-MEDIATED SUBVERSION OF PROGRAMMED CELL-DEATH AS A MECHANISM FOR IMMUNE DYSREGULATION
    AMEISEN, JC
    ESTAQUIER, J
    IDZIOREK, T
    [J]. IMMUNOLOGICAL REVIEWS, 1994, 142 : 9 - 51
  • [3] Upregulation of fas ligand expression by human immunodeficiency virus in human macrophages mediates apoptosis of uninfected T lymphocytes
    Badley, AD
    McElhinny, JA
    Leibson, PJ
    Lynch, DH
    Alderson, MR
    Paya, CV
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (01) : 199 - 206
  • [4] Macrophage-dependent apoptosis of CD4(+) T lymphocytes from HIV-infected individuals is mediated by FasL and tumor necrosis factor
    Badley, AD
    Dockrell, D
    Simpson, M
    Schut, R
    Lynch, DH
    Leibson, P
    Paya, CV
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) : 55 - 64
  • [5] Baumler CB, 1996, BLOOD, V88, P1741
  • [6] A ROLE FOR CD95 LIGAND IN PREVENTING GRAFT-REJECTION
    BELLGRAU, D
    GOLD, D
    SELAWRY, H
    MOORE, J
    FRANZUSOFF, A
    DUKE, RC
    [J]. NATURE, 1995, 377 (6550) : 630 - 632
  • [7] NOMENCLATURE FOR PEPTIDE FRAGMENT IONS (POSITIVE-IONS)
    BIEMANN, K
    [J]. METHODS IN ENZYMOLOGY, 1990, 193 : 886 - 887
  • [8] 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
  • [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] CAR1, a TNFR-related protein, is a cellular receptor for cytopathic avian leukosis sarcoma viruses and mediates apoptosis
    Brojatsch, J
    Naughton, J
    Rolls, MM
    Zingler, K
    Young, JAT
    [J]. CELL, 1996, 87 (05) : 845 - 855