Apparent species differences in the kinetic properties of P2X7 receptors

被引:65
作者
Hibell, AD [1 ]
Kidd, EJ [1 ]
Chessell, IP [1 ]
Humphrey, PPA [1 ]
Michel, AD [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Glaxo Inst Appl Pharmacol, Cambridge CB2 1QJ, England
关键词
P2X(7); ATP; ion channel;
D O I
10.1038/sj.bjp.0703302
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Apparent species differences in the responses of recombinant P2X(7) receptors to repeated application of 2'- and 3'-O-(4-benzoylbenzoyl)-ATP (BzATP) have been investigated. 2 Repeated application of 100 mu M BzATP resulted in a progressive increase in current magnitude (current growth) at mouse and human, but not rat P2X(7) receptors. 3 Current growth was thought to reflect progressive dilation of the P2X(7) ion-channel to a pore permeable to large molecules (MW < 900), suggesting that channel dilation was not occurring at the rat P2X(7) receptor. However, 100 mu M BzATP produced a rapid influx of YO-PRO-1 (MW375) in cells expressing rat or human P2X(7) receptors. 4 There were, however, species differences in agonist potency such that 100 mu M BzATP was a supra-maximal concentration at rat, but not human or mouse, P2X(7) receptors. Importantly, when sub-maximal concentrations of BzATP or ATP were examined, current growth occurred at rat P2X(7) receptors. 5 The rate of current growth and YO-PRO-1 accumulation increased with agonist concentration and appeared more rapid at rat and human, than at mouse P2X(7) receptors. 6 The potency of BzATP and ATP was 1.5-10 fold lower in naive cells than in cells repeatedly exposed to ATP. 7 This study demonstrates that current growth occurs at mouse, rat and human P2X(7) receptors but only when using sub-maximal concentrations of agonist. Previously, current growth was thought to reflect the progressive increase in pore diameter of the P2X(7) receptor ion channel, however, the results of this study suggest a progressive increase in agonist potency may also contribute.
引用
收藏
页码:167 / 173
页数:7
相关论文
共 18 条
  • [1] Braun N, 1998, J NEUROSCI, V18, P4891
  • [2] Blockade of human P2X7 receptor function with a monoclonal antibody
    Buell, G
    Chessell, IP
    Michel, AD
    Colo, G
    Salazzo, M
    Herren, S
    Gretener, D
    Grahames, C
    Kaur, R
    Kosco-Vilbois, MH
    Humphrey, PPA
    [J]. BLOOD, 1998, 92 (10) : 3521 - 3528
  • [3] Chessell I. P., 1999, British Journal of Pharmacology, V126, p19P
  • [4] Cloning and functional characterisation of the mouse P2X7 receptor
    Chessell, IP
    Simon, J
    Hibell, AD
    Michel, AD
    Barnard, EA
    Humphrey, PPA
    [J]. FEBS LETTERS, 1998, 439 (1-2) : 26 - 30
  • [5] Properties of the pore-forming P2X(7) purinoceptor in mouse NTW8 microglial cells
    Chessell, IP
    Michel, AD
    Humphrey, PPA
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (07) : 1429 - 1437
  • [6] A PATCH-CLAMP STUDY OF BOVINE CHROMAFFIN CELLS AND OF THEIR SENSITIVITY TO ACETYLCHOLINE
    FENWICK, EM
    MARTY, A
    NEHER, E
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1982, 331 (OCT): : 577 - 597
  • [7] IMPROVED PATCH-CLAMP TECHNIQUES FOR HIGH-RESOLUTION CURRENT RECORDING FROM CELLS AND CELL-FREE MEMBRANE PATCHES
    HAMILL, OP
    MARTY, A
    NEHER, E
    SAKMANN, B
    SIGWORTH, FJ
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1981, 391 (02): : 85 - 100
  • [8] HICKMAN SE, 1994, BLOOD, V84, P2452
  • [9] Isoquinolines as antagonists of the P2X7 nucleotide receptor:: High selectivity for the human versus rat receptor homologues
    Humphreys, BD
    Virginio, C
    Surprenant, A
    Rice, J
    Dubyak, GR
    [J]. MOLECULAR PHARMACOLOGY, 1998, 54 (01) : 22 - 32
  • [10] Release of adenosine and ATP in the brain of the freshwater turtle (Trachemys scripta) during long-term anoxia
    Lutz, PL
    Kabler, S
    [J]. BRAIN RESEARCH, 1997, 769 (02) : 281 - 286