Protease activated receptors: theme and variations

被引:193
作者
O'Brien, PJ
Molino, M
Kahn, M
Brass, LF
机构
[1] Univ Penn, Dept Med, Ctr Expt Therapeut, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pharmacol, Philadelphia, PA 19104 USA
[3] Ist Ric Farmacol Mario Negri, Consorzio Mario Negri Sud, I-66030 Santa Maria Imbaro, Italy
关键词
protease-activated receptors; thrombin; platelets; endothielial cells; G proteins; G protein coupled receptors;
D O I
10.1038/sj.onc.1204194
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
The four PAR family members are G protein coupled receptors that are normally activated by proteolytic exposure of an occult tethered ligand, Three of the family members are thrombin receptors, The fourth (PAR2) is not activated by thrombin, but can be activated by other proteases, including trypsin, tryptase and Factor Xa, This review focuses on recent information about the manner in which signaling through these receptors is initiated and terminated, including evidence for inter- as well as intramolecular modes of activation, and continuing efforts to identify additional, biologically-relevant proteases that can activate PAR family members.
引用
收藏
页码:1570 / 1581
页数:12
相关论文
共 118 条
  • [1] Proteinase activated receptor 2: role of extracellular loop 2 for ligand-mediated activation
    Al-Ani, B
    Saifeddine, M
    Kawabata, A
    Hollenberg, MD
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (05) : 1105 - 1113
  • [2] Extrapancreatic trypsin-2 cleaves proteinase-activated receptor-2
    Alm, AK
    Gagnemo-Persson, R
    Sorsa, T
    Sundelin, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (01) : 77 - 83
  • [3] Design, synthesis, and biological characterization of a peptide-mimetic antagonist for a tethered-ligand receptor
    Andrade-Gordon, P
    Mayanoff, BE
    Derian, CK
    Zhang, HC
    Addo, MF
    Darrow, AL
    Eckardt, AJ
    Hoekstra, WJ
    McComsey, DF
    Oksenberg, D
    Reynolds, EE
    Santulli, RJ
    Scarborough, RM
    Smith, CE
    White, KB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) : 12257 - 12262
  • [4] THE THROMBIN RECEPTOR EXTRACELLULAR DOMAIN CONTAINS SITES CRUCIAL FOR PEPTIDE LIGAND INDUCED ACTIVATION
    BAHOU, WF
    COLLER, BS
    POTTER, CL
    NORTON, KJ
    KUTOK, JL
    GOLIGORSKY, MS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) : 1405 - 1413
  • [5] IDENTIFICATION OF A NOVEL THROMBIN RECEPTOR SEQUENCE REQUIRED FOR ACTIVATION-DEPENDENT RESPONSES
    BAHOU, WF
    KUTOK, JL
    WONG, A
    POTTER, CL
    COLLER, BS
    [J]. BLOOD, 1994, 84 (12) : 4195 - 4202
  • [6] Development of potent thrombin receptor antagonist peptides
    Bernatowicz, MS
    Klimas, CE
    Hartl, KS
    Peluso, M
    Allegretto, NJ
    Seiler, SM
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (25) : 4879 - 4887
  • [7] Ligand cross-reactivity within the protease-activated receptor family
    Blackhart, BD
    Emilsson, K
    Nguyen, D
    Teng, W
    Martelli, AJ
    Nystedt, S
    Sundelin, J
    Scarborough, RM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) : 16466 - 16471
  • [8] Bohm SK, 1996, J BIOL CHEM, V271, P22003
  • [9] BRASS LF, 1992, J BIOL CHEM, V267, P6044
  • [10] BRASS LF, 1994, J BIOL CHEM, V269, P2943