Shields Shannon D, Mazario Javier, Skinner Kate, Basbaum Allan I
Departments of Anatomy and Physiology and W. M. Keck Foundation Center for Integrative Neuroscience, University of California San Francisco, San Francisco, CA 94158, USA.
Pain. 2007 Sep;131(1-2):8-20. doi: 10.1016/j.pain.2006.11.018. Epub 2007 Jan 25.
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.
水通道蛋白1(AQP1)是水通道蛋白家族的原型成员,该家族有助于肾脏、肺和其他组织中的水平衡。尽管关于水通道蛋白在神经系统中表达的证据有限,但AQP4在胶质细胞中表达,AQP9存在于一些神经元和胶质细胞的线粒体上。在本研究中,我们使用免疫组织化学方法显示,AQP1在背根神经节、三叉神经节和结状神经节的一群小直径初级感觉神经元中大量表达。AQP1免疫反应性在背根神经节细胞体以及初级传入神经元的外周和中央分支中都很丰富,并且与伤害感受器的标记物,特别是P物质和IB4共定位。背根神经节中AQP1的表达在胚胎第15.5天首次可检测到,这与大多数精细皮肤传入神经穿透背角的发育阶段相对应。电子显微镜显示,在浅表背角的无髓轴突、少数细直径有髓轴突和突触终末有密集的膜标记。由于这种受限且密集的表达表明AQP1参与伤害性处理,我们在一系列全面的急性和持续性疼痛测试中研究了野生型和AQP1基因敲除小鼠的行为反应。我们还在野生型和突变型小鼠中使用体内电生理学方法,测量伤害性刺激诱导的敏化前后,背角V层广动力范围神经元对热刺激的反应。迄今为止,我们尚未检测到表明AQP1对伤害性处理有功能贡献的差异表型。