在帕金森病患者中,参与视觉运动感知的星爆无突细胞失去了来自多巴胺能无突细胞的突触输入并退化。

IF 10.8 1区 医学 Q1 NEUROSCIENCES
Xavier Sánchez-Sáez, Isabel Ortuño-Lizarán, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca
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引用次数: 3

摘要

背景:帕金森病(PD)的主要临床症状特征是运动迟缓、震颤和其他运动缺陷。然而,非运动症状,如视觉障碍,可以在疾病的早期阶段被发现。这些症状之一是视觉运动知觉受损。因此,我们试图确定参与运动方向选择的主要细胞类型星爆无突细胞是否在PD中退化,以及多巴胺能系统是否与这种退化有关。方法:选取对照(n = 10)和PD (n = 9)供体人眼。利用免疫组织化学和共聚焦显微镜,我们量化了横截面和全视网膜上星爆无突细胞密度(胆碱乙酰转移酶[ChAT]阳性细胞)以及这些细胞与多巴胺能无突细胞(酪氨酸羟酶阳性细胞和囊泡单胺转运蛋白2阳性前突触)之间的关系。结果:首先,我们在人视网膜中发现了两种不同的ChAT细胞群,它们具有不同的ChAT免疫反应强度和不同的钙结合蛋白表达。这两个人群都受到PD的影响,与对照组相比,它们的密度降低了。此外,我们还首次报道了人类视网膜中多巴胺能无突细胞和chat阳性细胞之间的突触接触。我们发现,在PD视网膜中,多巴胺能突触接触到ChAT细胞的减少。结论:本研究提示帕金森病星爆无突细胞的变性与多巴胺能变性有关,多巴胺能无突细胞可调节星爆无突细胞的功能。由于运动感知回路在PD中受到影响,因此使用视觉测试对其进行评估可以为PD的诊断提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Starburst amacrine cells, involved in visual motion perception, loose their synaptic input from dopaminergic amacrine cells and degenerate in Parkinson's disease patients.

Starburst amacrine cells, involved in visual motion perception, loose their synaptic input from dopaminergic amacrine cells and degenerate in Parkinson's disease patients.

Starburst amacrine cells, involved in visual motion perception, loose their synaptic input from dopaminergic amacrine cells and degenerate in Parkinson's disease patients.

Starburst amacrine cells, involved in visual motion perception, loose their synaptic input from dopaminergic amacrine cells and degenerate in Parkinson's disease patients.

Background: The main clinical symptoms characteristic of Parkinson's disease (PD) are bradykinesia, tremor, and other motor deficits. However, non-motor symptoms, such as visual disturbances, can be identified at early stages of the disease. One of these symptoms is the impairment of visual motion perception. Hence, we sought to determine if the starburst amacrine cells, which are the main cellular type involved in motion direction selectivity, are degenerated in PD and if the dopaminergic system is related to this degeneration.

Methods: Human eyes from control (n = 10) and PD (n = 9) donors were available for this study. Using immunohistochemistry and confocal microscopy, we quantified starburst amacrine cell density (choline acetyltransferase [ChAT]-positive cells) and the relationship between these cells and dopaminergic amacrine cells (tyrosine hydroxylase-positive cells and vesicular monoamine transporter-2-positive presynapses) in cross-sections and wholemount retinas.

Results: First, we found two different ChAT amacrine populations in the human retina that presented different ChAT immunoreactivity intensity and different expression of calcium-binding proteins. Both populations are affected in PD and their density is reduced compared to controls. Also, we report, for the first time, synaptic contacts between dopaminergic amacrine cells and ChAT-positive cells in the human retina. We found that, in PD retinas, there is a reduction of the dopaminergic synaptic contacts into ChAT cells.

Conclusions: Taken together, this work indicates degeneration of starburst amacrine cells in PD related to dopaminergic degeneration and that dopaminergic amacrine cells could modulate the function of starburst amacrine cells. Since motion perception circuitries are affected in PD, their assessment using visual tests could provide new insights into the diagnosis of PD.

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来源期刊
Translational Neurodegeneration
Translational Neurodegeneration Neuroscience-Cognitive Neuroscience
CiteScore
19.50
自引率
0.80%
发文量
44
审稿时长
10 weeks
期刊介绍: Translational Neurodegeneration, an open-access, peer-reviewed journal, addresses all aspects of neurodegenerative diseases. It serves as a prominent platform for research, therapeutics, and education, fostering discussions and insights across basic, translational, and clinical research domains. Covering Parkinson's disease, Alzheimer's disease, and other neurodegenerative conditions, it welcomes contributions on epidemiology, pathogenesis, diagnosis, prevention, drug development, rehabilitation, and drug delivery. Scientists, clinicians, and physician-scientists are encouraged to share their work in this specialized journal tailored to their fields.
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