Regulation of adenosine 5′-triphosphate (ATP)-gated P2X4 receptors on tracheal smooth muscle cells

被引:15
|
作者
Nagaoka, Miyuki [2 ]
Nara, Masayuki [1 ]
Tamada, Tsutomu [2 ]
Kume, Hiroaki [3 ]
Oguma, Tetsuya [3 ]
Kikuchi, Toshiaki [4 ]
Zaini, Jamal [4 ]
Moriya, Takuya [5 ]
Ichinose, Masakazu [6 ]
Tamura, Gen [2 ]
Hattori, Toshio [2 ]
机构
[1] Tohoku Univ, Sch Med, Div Comprehens Med, Dept Internal Med,Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Sch Med, Div Infect & Resp Dis, Dept Internal Med,Aoba Ku, Sendai, Miyagi 9808574, Japan
[3] Nagoya Univ, Sch Med, Div Resp Med, Dept Med,Showa Ku, Nagoya, Aichi 466, Japan
[4] Tohoku Univ, Sch Med, Div Resp Med, Dept Internal Med, Sendai, Miyagi 9808574, Japan
[5] Kawasaki Med Sch, Dept Pathol, Kurashiki, Okayama 70101, Japan
[6] Wakayama Med Univ, Dept Internal Med 3, Wakayama, Japan
关键词
Purinergic receptor; Airway smooth muscle; Ivermectin; EXTRACELLULAR ATP; SIGNAL-TRANSDUCTION; CA2+ SENSITIZATION; CATION CHANNELS; CURRENTS; IDENTIFICATION; INHIBITOR; AIRWAYS; INFLUX; ENTRY;
D O I
10.1016/j.resp.2009.02.002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We examined the effects of extracellular adenosine 5'-triphosphate (ATP) on single airway smooth muscle (ASM) cells from porcine trachea using a patch-clamp technique. ATP induced a sustained inward current. Phospholipase C inhibitor U-73122 failed to inhibit the current, suggesting the involvement of P2X receptor. A specific effecter of P2X(4), ivermectin, augmented the current indicating the existence of P2X(4) receptors. Immunohistochemistry and reverse transcription/polymerase chain reaction analysis and Western blot analysis also showed the distribution of the P2X(4) receptors. The inward current was reduced by SKF-96365, an inhibitor of both voltage-dependent Ca2+ channels (VDCCs) and voltage-independent Ca2+ channels, although a VDCC antagonist, verapamil, did not affect the current. SKF-96365 caused complete suppression of both the increase in the intracellular Ca2+ concentration and the contraction of ASM cells induced by ATP. Our results demonstrate that P2X(4) receptors exist on ASM and that the receptors are responsible for Ca2+ influx. These findings suggest that the Ca2+ influx regulated by P2X(4) receptors plays an important role in ASM contraction by a pathway distinct from VDCC. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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