Kinetics of P2X7 receptor-operated single channels currents

被引:56
作者
Riedel, T.
Lozinsky, I.
Schmalzing, G.
Markwardt, F. [1 ]
机构
[1] Univ Halle Wittenberg, Julius Bernstein Inst Physiol, D-4010 Halle, Germany
[2] Univ Kentucky, Dept Internal Med, Lexington, KY 40506 USA
[3] Rhein Westfal TH Aachen, Dept Mol Pharmacol, D-5100 Aachen, Germany
关键词
D O I
10.1529/biophysj.106.091413
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Human P2X(7) receptors were expressed in Xenopus laevis oocytes and single channels were recorded using the patch-clamp technique in the outside- out configuration. ATP(4-) evoked two types of P2X(7) receptor-mediated single channel currents characterized by short-lived and long-lived openings. The short- and long-lasting open states had mean open times of similar to 5 and similar to 20 ms and slope conductances near -60 mV of 9 and 13 pS, respectively. The open probabilities of the short and long openings were strongly [ ATP(4-)]- dependent with EC50 values of similar to 0.3 mM and similar to 0.1 mM ATP(4-), respectively. The channel kinetics did not change significantly during sustained P2X(7) receptor activation for several minutes, as was also observed in recordings in the cell-attached patch-clamp configuration. Activation and deactivation of the short openings followed exponential time courses with time constants in the range of 20 ms, and displayed a shallow [ ATP(4-)] dependence of the activation process. The kinetics of the short channel openings at negative membrane potentials fitted well to a linear C-C-C-O model with two ATP(4-) binding steps at equal binding sites with a dissociation constant K-d of 139 mu M.
引用
收藏
页码:2377 / 2391
页数:15
相关论文
共 39 条
  • [1] Tyrosine phosphorylation of HSP90 within the P2X7 receptor complex negatively regulates P2X7 receptors
    Adinolfi, E
    Kim, M
    Young, MT
    Di Virgilio, F
    Surprenant, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) : 37344 - 37351
  • [2] HETEROGENEOUS KINETIC-PROPERTIES OF ACETYLCHOLINE-RECEPTOR CHANNELS IN XENOPUS MYOCYTES
    AUERBACH, A
    LINGLE, CJ
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1986, 378 : 119 - 140
  • [3] Glu496 Ala polymorphism of human P2X7 receptor does not affect its electrophysiological phenotype
    Boldt, W
    Klapperstück, M
    Büttner, C
    Sadtler, S
    Schmalzing, N
    Markwardt, F
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 284 (03): : C749 - C756
  • [4] NONSELECTIVE CATIONIC CURRENTS ELICITED BY EXTRACELLULAR ATP IN HUMAN AND B-LYMPHOCYTES
    BRETSCHNEIDER, F
    KLAPPERSTUCK, M
    LOHN, M
    MARKWARDT, F
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1995, 429 (05): : 691 - 698
  • [5] Bretschneider F, 1999, Methods Enzymol, V294, P180
  • [6] Dynamics of P2X7 receptor pore dilation:: Pharmacological and functional consequences
    Chessell, IP
    Grahames, CBA
    Michel, AD
    Humphrey, PPA
    [J]. DRUG DEVELOPMENT RESEARCH, 2001, 53 (2-3) : 60 - 65
  • [7] 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
  • [8] ATP stimulation of P2X7 receptors activates three different ionic conductances on cultured mouse Schwann cells
    Colomar, A
    Amédée, T
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (06) : 927 - 936
  • [9] FAST EVENTS IN SINGLE-CHANNEL CURRENTS ACTIVATED BY ACETYLCHOLINE AND ITS ANALOGS AT THE FROG-MUSCLE ENDPLATE
    COLQUHOUN, D
    SAKMANN, B
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1985, 369 (DEC): : 501 - &
  • [10] RELAXATION AND FLUCTUATIONS OF MEMBRANE CURRENTS THAT FLOW THROUGH DRUG-OPERATED CHANNELS
    COLQUHOUN, D
    HAWKES, AG
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1977, 199 (1135): : 231 - 262