Functional Expression of an Osmosensitive Cation Channel, Transient Receptor Potential Vanilloid 4, in Rat Vestibular Ganglia

Takefumi Kamakura, M. Kondo, Y. Koyama, Yukiko Hanada, Y. Ishida, Yukiko Nakamura, Takahiro Yamada, Y. Takimoto, T. Kitahara, Y. Ozono, A. Horii, T. Imai, H. Inohara, S. Shimada
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引用次数: 4

Abstract

Transient receptor potential vanilloid (TRPV) 4 is a nonselective cation channel expressed in sensory neurons such as those in the dorsal root and trigeminal ganglia, kidney, and inner ear. TRPV4 is activated by mechanical stress, heat, low osmotic pressure, low pH, and phorbol derivatives such as 4α-phorbol 12,13-didecanoate (4α-PDD). We investigated the expression of TRPV4 in rat vestibular ganglion (VG) neurons. The TRPV4 gene was successfully amplified from VG neuron mRNA using reverse-transcription polymerase chain reaction. Furthermore, immunoblotting showed positive expression of TRPV4 protein in VG neurons. Immunohistochemistry indicated that TRPV4 was localized predominantly on the plasma membrane of VG neurons. Calcium (Ca2+) imaging of VG neurons showed that 4α-PDD and/or hypotonic stimuli caused an increase in intracellular Ca2+ concentration ([Ca2+]i) that was almost completely inhibited by ruthenium red, a selective antagonist of TRPV channels. Interestingly, a [Ca2+]i increase was evoked by both hypotonic stimuli and 4α-PDD in approximately 38% of VG neurons. These data indicate that TRPV4 is functionally expressed in VG neurons as an ion channel and that TRPV4 likely participates in VG neurons for vestibular neurotransmission as an osmoreceptor and/or mechanoreceptor.
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渗透敏感阳离子通道瞬时受体电位香草蛋白4在大鼠前庭神经节中的功能表达
瞬时受体电位香草蛋白(TRPV) 4是一种非选择性阳离子通道,在背根、三叉神经节、肾脏和内耳等感觉神经元中表达。TRPV4被机械应力、热、低渗透压、低pH和4α-phorbol 12,13-didecanoate (4α-PDD)等phorbol衍生物激活。我们研究了TRPV4在大鼠前庭神经节(VG)神经元中的表达。利用逆转录聚合酶链式反应成功地从VG神经元mRNA中扩增出TRPV4基因。此外,免疫印迹显示TRPV4蛋白在VG神经元中呈阳性表达。免疫组化显示TRPV4主要定位于VG神经元的质膜上。VG神经元的钙(Ca2+)成像显示,4α-PDD和/或低压刺激引起细胞内Ca2+浓度([Ca2+]i)的增加,而这种增加几乎完全被TRPV通道的选择性拮抗剂钌红所抑制。有趣的是,低渗刺激和4α-PDD在大约38%的VG神经元中引起[Ca2+]i增加。这些数据表明,TRPV4在VG神经元中作为离子通道功能表达,并且TRPV4可能作为渗透受体和/或机械受体参与VG神经元前庭神经传递。
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