Puthussery Theresa, Yee Peter, Vingrys Algis J, Fletcher Erica L
Department of Anatomy and Cell Biology, The University of Melbourne, Parkville 3010 Victoria, Australia.
Eur J Neurosci. 2006 Jul;24(1):7-19. doi: 10.1111/j.1460-9568.2006.04895.x.
Extracellular ATP mediates fast excitatory neurotransmission in many regions of the central nervous system through activation of P2X receptors. Although several P2X receptor subunits have been identified in the mammalian retina, little is known about the functional role of these receptors in retinal signalling. The purpose of the present study was to investigate whether purinergic P2X(7) receptors are involved in outer retinal processing by assessing receptor localization, degradation of extracellular ATP and the effect of functional activation of P2X(7) receptors on the electroretinogram (ERG). Using light and electron microscopy, we demonstrated that P2X(7) receptors are expressed postsynaptically on horizontal cell processes as well as presynaptically on photoreceptor synaptic terminals in both the rat and marmoset retina. Using an enzyme cytochemical method, we showed that ecto-ATPases are active in the outer plexiform layer of the rat retina, providing a mechanism by which purinergic synaptic transmission can be rapidly terminated. Finally, we evaluated the role of P2X(7) receptors in retinal function by assessing changes to the ERG response of rats after intravitreal delivery of the P2X(7) receptor agonist benzoyl benzoyl ATP (BzATP). Intravitreal injection of BzATP resulted in a sustained increase (up to 58%) in the amplitude of the photoreceptor-derived a-wave of the ERG. In contrast, BzATP caused a transient reduction in the rod- and cone-derived postreceptoral responses. These results provide three lines of evidence for the involvement of extracellular purines in outer retinal processing.
细胞外ATP通过激活P2X受体在中枢神经系统的许多区域介导快速兴奋性神经传递。尽管在哺乳动物视网膜中已鉴定出几种P2X受体亚基,但这些受体在视网膜信号传导中的功能作用仍知之甚少。本研究的目的是通过评估受体定位、细胞外ATP的降解以及P2X(7)受体功能激活对视网膜电图(ERG)的影响,来研究嘌呤能P2X(7)受体是否参与视网膜外层处理。利用光学显微镜和电子显微镜,我们证明在大鼠和狨猴视网膜中,P2X(7)受体在水平细胞突起的突触后以及光感受器突触终末的突触前均有表达。利用酶细胞化学方法,我们表明外切ATP酶在大鼠视网膜的外网状层中具有活性,这为嘌呤能突触传递能够快速终止提供了一种机制。最后,我们通过评估玻璃体内注射P2X(7)受体激动剂苯甲酰苯甲酰ATP(BzATP)后大鼠ERG反应的变化,来评估P2X(7)受体在视网膜功能中的作用。玻璃体内注射BzATP导致ERG中光感受器来源的a波振幅持续增加(高达58%)。相比之下,BzATP导致杆体和锥体来源的感受器后反应短暂降低。这些结果为细胞外嘌呤参与视网膜外层处理提供了三条证据。