Pore properties and pharmacological features of the P2X receptor channel in airway ciliated cells

被引:69
作者
Ma, WY
Korngreen, A
Weil, S
Cohen, EBT
Priel, A
Kuzin, L
Silberberg, SD
机构
[1] Ben Gurion Univ Negev, Dept Chem, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Zlotowski Ctr Neurosci, IL-84105 Beer Sheva, Israel
[3] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
[4] Bar Ilan Univ, Fac Life Sci, IL-52900 Ramat Gan, Israel
[5] Bar Ilan Univ, Leslie & Susan Gonda Interdisciplinary Brain Res, IL-52900 Ramat Gan, Israel
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2006年 / 571卷 / 03期
关键词
D O I
10.1113/jphysiol.2005.103408
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Airway ciliated cells express an ATP-gated P2X receptor channel of unknown subunit composition (P2X(cilia)) which is modulated by Na+ and by long exposures to ATP. P2X(cilia) was investigated by recording currents from freshly dissociated rabbit airway ciliated cells with the patch-clamp technique in the whole-cell configuration. During the initial continuous exposure to extracellular ATP, P2X(cilia) currents gradually increase in magnitude (priming), yet the permeability to N-methyl-D-glucamine (NMDG) does not change, indicating that priming does not arise from a progressive change in pore diameter. Na+, which readily permeates P2X(cilia) receptor channels, was found to inhibit the channel extracellular to the electric field. The rank order of permeability to various monovalent cations is: Li+, Na+, K+, Rb+, Cs+, NMDG(+) and TEA(+), with a relative permeability of 1.35, 1.0, 0.99, 0.91, 0.79, 0.19 and 0.10, respectively. The rank order for the alkali cations follows an Eisenman series XI for a high-strength field site. Ca2+ has been estimated to be 7-fold more permeant than Na+. The rise in [Ca2+](i) in ciliated cells, induced by the activation of P2X(cilia), is largely inhibited by either Brilliant Blue G or KN-62, indicating that P2X(7) may be a part of P2X(cilia). P2X(cilia) is augmented by Zn2+ and by ivermectin, and P2X(4) receptor protein is detected by immunolabelling at the basal half of the cilia, strongly suggesting that P2X(4) is a component of P2X(cilia) receptor channels. Taken together, these results suggest that P2X(cilia) is either assembled from P2X(4) and P2X(7) subunits, or formed from modified P2X(4) subunits.
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页码:503 / 517
页数:15
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