Retinal degeneration increases inter-trial variabilities of light-evoked spiking activities in ganglion cells

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Da Eun Kim , Sein Kim , Minju Kim , Byoung-Kyong Min , Maesoon Im
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引用次数: 0

Abstract

Retinal ganglion cells (RGCs) transmit visual information to the brain in the form of spike trains, which form visual perception. The reliabilities of spike timing and count are thought to play a crucial role in generating stable percepts. However, the effect of retinal degeneration on spike reproducibility remains underexplored. In this study, we examined longitudinal changes of both spike timing and count across different RGC types in response to repeated presentations of an identical light stimulus in retinal degeneration 10 (rd10) mice (B6.CXBl-Pde6brd10/J), a well-established model of retinitis pigmentosa (RP).
We recorded the spiking responses of RGC populations to repeated white flashes using 256-channel multi-electrode array (MEA) at four rd10 age groups representing various stages of retinal degeneration. Our experimental results revealed a significant reduction in both spike timing and count consistencies compared to those in wild-type RGC recordings. Furthermore, the inter-trial variability patterns of different RGC types were found to differ throughout the degeneration process. For instance, when the spike time tiling coefficient (STTC) was used to evaluate inter-trial spike timing consistency, contrast-sensitive RGCs (ON, OFF, and ON-OFF types) exhibited a systematic decrease in spike timing consistency as degeneration progressed, whereas the remaining units did not show similar trends. Thus, we concluded that light-evoked spike trains become less consistent as degeneration progresses, with variability in spike timing and spike count varying across cell types.
Given the critical role of spiking reliability in visual perception, our findings highlight the importance of accounting for cell type-specific degeneration patterns and inter-trial spiking inconsistencies when developing visual rehabilitation therapies to achieve enhanced performance. The underlying mechanism(s) driving the inter-trial spiking inconsistencies warrant further investigation.
视网膜变性增加了神经节细胞中光诱发尖峰活动的试验间变异性
视网膜神经节细胞(RGCs)以脉冲序列的形式将视觉信息传递给大脑,从而形成视觉感知。脉冲时间和计数的可靠性被认为在产生稳定的感知中起着至关重要的作用。然而,视网膜变性对尖峰再现性的影响仍未得到充分研究。在这项研究中,我们在视网膜变性10 (rd10)小鼠(B6.CXBl-Pde6brd10/J)中检测了不同RGC类型在重复呈现相同光刺激时的脉冲时间和计数的纵向变化,视网膜变性10 (rd10)是一种成熟的色素性视网膜炎(RP)模型。我们使用256通道多电极阵列(MEA)记录了RGC人群对重复白色闪光的尖峰反应,这些尖峰反应代表了四个rd10年龄组的视网膜变性的不同阶段。我们的实验结果显示,与野生型RGC记录相比,尖峰计时和计数一致性都显着减少。此外,不同RGC类型的试验间变异模式在整个变性过程中存在差异。例如,当使用峰值时间平纹系数(STTC)来评估试验间峰值时间一致性时,对比敏感的rgc (ON、OFF和ON-OFF类型)随着退化的进展呈现出系统性的峰值时间一致性下降,而其余单元则没有表现出类似的趋势。因此,我们得出的结论是,随着变性的进展,光诱发的尖峰序列变得不那么一致,在不同的细胞类型中,尖峰时间和尖峰计数存在差异。鉴于脉冲可靠性在视觉感知中的关键作用,我们的研究结果强调了在开发视觉康复疗法以实现增强性能时,考虑细胞类型特异性变性模式和试验间脉冲不一致性的重要性。导致试验间尖峰不一致的潜在机制值得进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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