Expression level dependent changes in the properties of P2X2 receptors

被引:30
作者
Clyne, JD [1 ]
Brown, TC [1 ]
Hume, RI [1 ]
机构
[1] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
关键词
P2X; purinergic; zinc; pH; Xenopus; aggregation;
D O I
10.1016/S0028-3908(02)00406-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The currents of P2X(2) receptors expressed in Xenopus oocytes or HEK293 cells show significant cell-to-cell variation in many properties including the rate of desensitization and the magnitude of potentiation by zinc or acidic pH. In this study, we examined whether differences in expression levels underlie this variability. We injected Xenopus oocytes with different concentrations of RNA encoding rat P2X(2) to give a wide range of maximum current amplitudes, and then measured the potentiation of responses to 10 muM adenosine 5'-triphosphate (ATP) by zinc or acidic pH. Individual oocytes showed potentiation ratios that ranged from 1.4- to 25-fold. Oocytes with small amplitude responses to a saturating concentration of ATP tended to have larger potentiation ratios than oocytes with large amplitude responses. This phenomenon was explained by an inverse correlation between the EC50 for ATP and the maximum current amplitude, with the EC50 decreasing from about 37 to 7 muM as expression level increased. In contrast, the Hill coefficient was not correlated with the maximum current amplitude. Truncated receptors lacking the last 76 amino acids also showed an inverse correlation between the EC50 and the maximum current amplitude. Thus, the interactions that cause expression-dependent changes in P2X(2) receptor properties must involve domains proximal to position H397. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:403 / 412
页数:10
相关论文
共 43 条
[31]   Molecular mechanisms of glutamate receptor clustering at excitatory synapses [J].
O'Brien, RJ ;
Lau, LF ;
Huganir, RL .
CURRENT OPINION IN NEUROBIOLOGY, 1998, 8 (03) :364-369
[32]   P2X (purinergic) receptor redistribution in rabbit aorta following injury to endothelial cells and cholesterol feeding [J].
Pulvirenti, TJ ;
Yin, JL ;
Chaufour, X ;
McLachlan, C ;
Hambly, BD ;
Bennett, MR ;
Barden, JA .
JOURNAL OF NEUROCYTOLOGY, 2000, 29 (09) :623-631
[33]  
Ralevic V, 1998, PHARMACOL REV, V50, P413
[34]   Synaptic P2X receptors [J].
Robertson, SJ ;
Ennion, SJ ;
Evans, RJ ;
Edwards, FA .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :378-386
[35]   PDZ domains and the organization of supramolecular complexes [J].
Sheng, M ;
Sala, C .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :1-29
[36]   Contribution of individual subunits to the multimeric P2X2 receptor:: Estimates based on methanethiosulfonate block at T336C [J].
Stoop, R ;
Thomas, S ;
Rassendren, F ;
Kawashima, E ;
Buell, G ;
Surprenant, A ;
North, RA .
MOLECULAR PHARMACOLOGY, 1999, 56 (05) :973-981
[37]   Different sensitivities to pH of ATP-induced currents at four cloned P2X receptors [J].
Stoop, R ;
Surprenant, A ;
North, RA .
JOURNAL OF NEUROPHYSIOLOGY, 1997, 78 (04) :1837-1840
[38]   EXPRESSION OF THE HUMAN GLYCINE RECEPTOR ALPHA-1-SUBUNIT IN XENOPUS-OOCYTES - APPARENT AFFINITIES OF AGONISTS INCREASE AT HIGH RECEPTOR DENSITY [J].
TALEB, O ;
BETZ, H .
EMBO JOURNAL, 1994, 13 (06) :1318-1324
[39]   Pore dilation of neuronal P2X receptor channels [J].
Virginio, C ;
MacKenzie, A ;
Rassendren, FA ;
North, RA ;
Surprenant, A .
NATURE NEUROSCIENCE, 1999, 2 (04) :315-321
[40]   Single amino acid residue influences the distribution pattern of an inwardly rectifying potassium channel in polarized cells [J].
Wild, K ;
Paysan, J .
CELL AND TISSUE RESEARCH, 2002, 307 (01) :47-55