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首页> 外文期刊>Pain. >Anatomical and functional analysis of aquaporin 1, a water channel in primary afferent neurons.
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Anatomical and functional analysis of aquaporin 1, a water channel in primary afferent neurons.

机译:水通道蛋白1(原发传入神经元中的水通道)的解剖学和功能分析。

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Aquaporin 1 (AQP1) is the archetypal member of a family of water channel proteins that contribute to water homeostasis in kidney, lung, and other tissues. Although there is limited evidence that aquaporins are expressed in the nervous system, AQP4 is expressed in glia and AQP9 is present on some neuronal and glial mitochondria. In the present study, we used immunohistochemistry to show that AQP1 is heavily expressed in a population of small diameter primary sensory neurons of dorsal root, trigeminal, and nodose ganglia. AQP1 immunoreactivity is abundant in DRG cell bodies and in both the peripheral and central branches of primary afferent neurons, and colocalizes with markers of nociceptors, notably substance P and IB4. AQP1 expression in DRG is first detectable at embryonic day 15.5, which corresponds to the developmental stage when the majority of fine cutaneous afferents penetrate the dorsal horn. Electron microscopy revealed dense membrane labeling of unmyelinated axons, a few fine diameter myelinated axons, and synaptic terminals in the superficial dorsal horn. Because this restricted and dense expression suggested that AQP1 contributes to nociceptive processing, we studied behavioral responses of wildtype and AQP1 -/- mice in a comprehensive battery of acute and persistent pain tests. We also used in vivo electrophysiology in wildtype and mutant mice to measure the responses of wide dynamic range neurons in lamina V of the dorsal horn to thermal stimulation before and after noxious stimulus-induced sensitization. To date we have not detected a differential phenotype suggestive of a functional contribution of AQP1 to nociceptive processing.
机译:水通道蛋白1(AQP1)是水通道蛋白家族的原型成员,该蛋白有助于肾脏,肺和其他组织中的水体内平衡。尽管很少有证据表明水通道蛋白在神经系统中表达,但AQP4在胶质细胞中表达,而AQP9在某些神经元和神经胶质线粒体中存在。在本研究中,我们使用免疫组织化学显示AQP1在背根,三叉神经节和结节神经节的小直径初级感觉神经元群体中大量表达。 AQP1免疫反应性在DRG细胞体以及原发传入神经元的外周和中央分支中均很丰富,并且与伤害感受器的标记物共定位,尤其是P和IB4物质。 DRG中的AQP1表达首先在胚胎第15.5天被检测到,这对应于大多数精细皮肤传入神经穿透背角的发育阶段。电子显微镜显示未髓鞘轴突的致密膜标记,一些细直径的髓鞘轴突和浅表背角的突触末端。因为这种受限和密集的表达表明AQP1有助于伤害感受过程,所以我们在一系列急性和持续性疼痛测试中研究了野生型和AQP1-/-小鼠的行为反应。我们还在野生型和突变型小鼠中使用了体内电生理学,以测量在有害刺激诱发的敏化前后,背角V板层V的宽动态范围神经元对热刺激的反应。迄今为止,我们还没有发现表明AQP1对伤害感受过程有功能贡献的差异表型。

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