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一氧化氮合酶在树鼩视网膜中的定位。

Localization of nitric oxide synthase in the tree shrew retina.

作者信息

Cao Q L, Murphy H A, Petry H M

机构信息

Department of Psychology, University of Louisville, KY 40292, USA.

出版信息

Vis Neurosci. 1999 May-Jun;16(3):399-409. doi: 10.1017/s0952523899163016.

Abstract

Nitric oxide (NO) is a novel neuronal messenger that likely influences retinal function by activating retinal guanylyl cyclase to increase levels of cGMP. In the present study, the localization of neuronal nitric oxide synthase (nNOS, Type I NOS) in the cone-dominant tree shrew retina was studied using NADPH-d histochemistry and nNOS immunocytochemistry. Both NADPH-d and nNOS-immunoreactivity (IR) labeled the inner segments of rods and the myoids of a regular subpopulation of cones, with their corresponding nuclei outlined. The labeled cone myoids were co-localized with a marker for short-wave-sensitive (SWS) cones (S-antigen) and also displayed the regular triangular packing and density (7%) characteristic of SWS cones in tree shrew and other mammalian retinas. These measures confirmed the identity of the labeled cones as SWS cones. Photoreceptor ellipsoids of all cones were strongly labeled by NADPH-d reactivity, but lacked nNOS-IR. Another novel finding in tree shrew retina was that both NADPH-d and nNOS-IR labeled Muller cells, which have not been labeled by nNOS-IR in other mammalian retinas. Consistent with findings in rod-dominant retinas, two types of amacrine cells at the vitreal edge of the inner nuclear layer and a subpopulation of displaced amacrine cells at the scleral edge of the ganglion cell layer were labeled by both NADPH-d and nNOS-IR. Processes of these labeled cells were seen to extend into the inner plexiform layer, where dense punctate label was seen, especially in the central sublamina. These results show that localization of NOS in the cone-dominant tree shrew retina shares some common properties with rod-dominant mammalian retinas, but also shows some species-specific characteristics. The new finding of nNOS localization in tree shrew SWS cones and rods, but not in other cones, raises interesting questions about the roles of NO in the earliest level of visual processing.

摘要

一氧化氮(NO)是一种新型神经信使,可能通过激活视网膜鸟苷酸环化酶以增加环磷酸鸟苷(cGMP)水平来影响视网膜功能。在本研究中,使用还原型辅酶II-黄递酶(NADPH-d)组织化学和神经元型一氧化氮合酶(nNOS,I型一氧化氮合酶)免疫细胞化学方法研究了视锥细胞占主导的树鼩视网膜中nNOS的定位。NADPH-d和nNOS免疫反应性(IR)均标记了视杆细胞的内段和一部分规则的视锥细胞的肌样体,并勾勒出了它们相应的细胞核。标记的视锥细胞肌样体与短波敏感(SWS)视锥细胞的标志物(S抗原)共定位,并且还呈现出树鼩和其他哺乳动物视网膜中SWS视锥细胞特有的规则三角形排列和密度(7%)。这些测量结果证实了标记的视锥细胞为SWS视锥细胞。所有视锥细胞的光感受器椭球体均被NADPH-d反应性强烈标记,但缺乏nNOS-IR。树鼩视网膜中的另一个新发现是,NADPH-d和nNOS-IR均标记了Muller细胞,而在其他哺乳动物视网膜中Muller细胞未被nNOS-IR标记。与视杆细胞占主导的视网膜中的发现一致,内核层玻璃体边缘的两种无长突细胞以及神经节细胞层巩膜边缘的一部分移位无长突细胞均被NADPH-d和nNOS-IR标记。可见这些标记细胞的突起延伸至内网层,在内网层可见密集的点状标记,尤其是在中央亚层。这些结果表明,一氧化氮合酶在视锥细胞占主导的树鼩视网膜中的定位与视杆细胞占主导的哺乳动物视网膜有一些共同特性,但也表现出一些物种特异性特征。nNOS在树鼩SWS视锥细胞和视杆细胞中定位,而在其他视锥细胞中不定位这一新发现,引发了关于NO在视觉处理最早阶段作用的有趣问题。

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