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小鼠视网膜中颜色和黑视蛋白介导的反应。

Colour and melanopsin mediated responses in the murine retina.

作者信息

Mouland Joshua W, Watson Alex J, Martial Franck P, Lucas Robert J, Brown Timothy M

机构信息

Centre for Biological Timing, Faculty of Biology Medicine and Health, University of Manchester, Manchester, United Kingdom.

Division of Diabetes, Endocrinology and Gastroenterology, Faculty of Biology Medicine and Health, University of Manchester, Manchester, United Kingdom.

出版信息

Front Cell Neurosci. 2023 Mar 13;17:1114634. doi: 10.3389/fncel.2023.1114634. eCollection 2023.

Abstract

Intrinsically photosensitive retinal ganglion cells (ipRGCs) integrate melanopsin and rod/cone-mediated inputs to signal to the brain. Whilst originally identified as a cell type specialised for encoding ambient illumination, several lines of evidence indicate a strong association between colour discrimination and ipRGC-driven responses. Thus, cone-mediated colour opponent responses have been widely found across ipRGC target regions in the mouse brain and influence a key ipRGC-dependent function, circadian photoentrainment. Although ipRGCs exhibiting spectrally opponent responses have also been identified, the prevalence of such properties have not been systematically evaluated across the mouse retina or yet been found in ipRGC subtypes known to influence the circadian system. Indeed, there is still uncertainty around the overall prevalence of cone-dependent colour opponency across the mouse retina, given the strong retinal gradient in S and M-cone opsin (co)-expression and overlapping spectral sensitivities of most mouse opsins. To address this, we use photoreceptor isolating stimuli in multielectrode recordings from human red cone opsin knock-in mouse (Opn1mwR) retinas to systematically survey cone mediated responses and the occurrence of colour opponency across ganglion cell layer (GCL) neurons and identify ipRGCs based on spectral comparisons and/or the persistence of light responses under synaptic blockade. Despite detecting robust cone-mediated responses across the retina, we find cone opponency is rare, especially outside of the central retina (overall ~3% of GCL neurons). In keeping with previous suggestions we also see some evidence of rod-cone opponency (albeit even more rare under our experimental conditions), but find no evidence for any enrichment of cone (or rod) opponent responses among functionally identified ipRGCs. In summary, these data suggest the widespread appearance of cone-opponency across the mouse early visual system and ipRGC-related responses may be an emergent feature of central visual processing mechanisms.

摘要

内在光敏性视网膜神经节细胞(ipRGCs)整合黑视蛋白以及视杆/视锥介导的输入信号,向大脑发送信号。虽然最初被确定为一种专门用于编码环境光照的细胞类型,但多项证据表明,颜色辨别与ipRGC驱动的反应之间存在紧密联系。因此,视锥介导的颜色拮抗反应在小鼠大脑的ipRGC目标区域广泛存在,并影响一项关键的ipRGC依赖性功能——昼夜节律光同步化。尽管也已鉴定出表现出光谱拮抗反应的ipRGCs,但尚未在整个小鼠视网膜中系统评估此类特性的普遍性,也未在已知影响昼夜节律系统的ipRGC亚型中发现。实际上,鉴于S和M视锥视蛋白(共)表达存在强烈的视网膜梯度以及大多数小鼠视蛋白的光谱敏感性重叠,整个小鼠视网膜中视锥依赖性颜色拮抗的总体普遍性仍存在不确定性。为了解决这个问题,我们在人红色视锥视蛋白敲入小鼠(Opn1mwR)视网膜的多电极记录中使用光感受器分离刺激,以系统地调查视锥介导的反应以及神经节细胞层(GCL)神经元中颜色拮抗的发生情况,并基于光谱比较和/或突触阻断下光反应的持续性来识别ipRGCs。尽管在整个视网膜中检测到了强烈的视锥介导反应,但我们发现视锥拮抗很少见,尤其是在视网膜中央区域之外(GCL神经元总体约为3%)。与之前的推测一致,我们也看到了一些视杆 - 视锥拮抗的证据(尽管在我们的实验条件下更罕见),但在功能鉴定的ipRGCs中未发现任何视锥(或视杆)拮抗反应富集的证据。总之,这些数据表明,视锥拮抗在小鼠早期视觉系统中的广泛出现以及与ipRGC相关的反应可能是中枢视觉处理机制的一个新兴特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0f/10040579/93690dbbc875/fncel-17-1114634-g0001.jpg

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