Margulis A, Pozdnyakov N, Dang L, Sitaramayya A
Eye Research Institute, Oakland University, Rochester, MI 48309, USA.
Vis Neurosci. 1998 Sep-Oct;15(5):867-73. doi: 10.1017/s0952523898155098.
Cyclic GMP has been shown in recent years to directly activate ion channels in bipolar and ganglion cells, and to indirectly regulate coupling between horizontal cells, and between bipolar and amacrine cells. In all of these cases, the effects of cyclic GMP are mimicked by nitric oxide. An increase in calcium concentration stimulates the production of nitric oxide by neuronal and endothelial forms of nitric oxide synthase, which in turn activates soluble guanylate cyclases, enhancing the synthesis of cyclic GMP. Though some effects of nitric oxide do not involve cyclic GMP, the nitric oxide-cyclic GMP cascade is well recognized as a signaling mechanism in brain and other tissues. The widespread occurrence of nitric oxide/cyclic GMP-regulated ion channel activity in retinal neurons raises the possibility that nitric-oxide-sensitive soluble guanylate cyclases play an important role in cell-cell communication, and possibly, synaptic transmission. Immunohistochemical studies have indicated the presence of soluble guanylate cyclase in retinal synaptic layers, but such studies are not suitable for determination of the density or quantitative subcellular distribution of the enzyme. Microanalytical methods involving microdissection of frozen retina also showed the presence of cyclase activity in retinal plexiform layers but these methods did not permit distinction between nitric oxide-sensitive and insensitive cyclases. In this study, we fractionated retinal homogenate into the cytosolic and synaptosomal fractions and investigated the specific activity and distribution of soluble guanylate cyclase and nitric oxide synthase. The results show that both enzymes are present in the synaptosomal fractions derived from inner and outer plexiform layers. The synaptosomal fraction derived from inner retina was highly enriched in cyclase activity. Nitric oxide synthase activity was also higher in the inner than outer retinal synaptosomal fraction. The results suggest that the nitric oxide-cyclic GMP system is operational in both synaptic layers of retina and that it may play a more significant role in the inner retina.
近年来已表明,环鸟苷酸(cGMP)可直接激活双极细胞和神经节细胞中的离子通道,并间接调节水平细胞之间以及双极细胞与无长突细胞之间的耦合。在所有这些情况下,一氧化氮(NO)可模拟cGMP的作用。钙浓度的升高会刺激神经元型和内皮型一氧化氮合酶产生NO,进而激活可溶性鸟苷酸环化酶,增强cGMP的合成。尽管NO的某些作用不涉及cGMP,但NO-cGMP级联反应作为大脑和其他组织中的一种信号传导机制已得到广泛认可。视网膜神经元中广泛存在由NO/cGMP调节的离子通道活性,这增加了一种可能性,即对NO敏感的可溶性鸟苷酸环化酶在细胞间通讯以及可能的突触传递中发挥重要作用。免疫组织化学研究表明视网膜突触层中存在可溶性鸟苷酸环化酶,但此类研究并不适合确定该酶的密度或亚细胞定量分布。涉及冷冻视网膜显微切割的微量分析方法也显示视网膜神经纤维层中存在环化酶活性,但这些方法无法区分对NO敏感和不敏感的环化酶。在本研究中,我们将视网膜匀浆分离为胞质部分和突触体部分,并研究了可溶性鸟苷酸环化酶和一氧化氮合酶的比活性及分布。结果表明,这两种酶均存在于源自内、外神经纤维层的突触体部分中。源自视网膜内层的突触体部分的环化酶活性高度富集。视网膜内层突触体部分的一氧化氮合酶活性也高于外层。结果表明,NO-cGMP系统在视网膜的两个突触层中均起作用,并且可能在内层视网膜中发挥更重要的作用。