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没有证据表明狨猴视网膜存在与年龄相关的变化。

No evidence for age-related alterations in the marmoset retina.

作者信息

Haverkamp Silke, Reinhard Katja, Peichl Leo, Mietsch Matthias

机构信息

Department of Computational Neuroethology, Max Planck Institute for Neurobiology of Behavior-Caesar, Bonn, Germany.

Retinal Circuits and Optogenetics, Centre for Integrative Neuroscience, University of Tübingen, Tübingen, Germany.

出版信息

Front Neuroanat. 2022 Sep 2;16:945295. doi: 10.3389/fnana.2022.945295. eCollection 2022.

Abstract

The physiological aging process of the retina is accompanied by various and sometimes extensive changes: Macular degeneration, retinopathies and glaucoma are the most common findings in the elderly and can potentially lead to irreversible visual disablements up to blindness. To study the aging process and to identify possible therapeutic targets to counteract these diseases, the use of appropriate animal models is mandatory. Besides the most commonly used rodent species, a non-human primate, the common marmoset () emerged as a promising animal model of human aging over the last years. However, the visual aging process in this species is only partially characterized, especially with regard to retinal aberrations. Therefore, we assessed here for the first time potential changes in retinal morphology of the common marmoset of different age groups. By cell type specific immunolabeling, we analyzed different cell types and distributions, potential photoreceptor and ganglion cell loss, and structural reorganization. We detected no signs of age-related differences in staining patterns or densities of various cell populations. For example, there were no signs of photoreceptor degeneration, and there was only minimal sprouting of rod bipolar cells in aged retinas. Altogether, we describe here the maintenance of a stable neuronal architecture, distribution and number of different cell populations with only mild aberrations during the aging process in the common marmoset retina. These findings are in stark contrast to previously reported findings in rodent species and humans and deserve further investigations to identify the underlying mechanisms and possible therapeutic targets.

摘要

视网膜的生理性衰老过程伴随着各种各样、有时甚至是广泛的变化:黄斑变性、视网膜病变和青光眼是老年人最常见的病症,有可能导致直至失明的不可逆视力损伤。为了研究衰老过程并确定对抗这些疾病的可能治疗靶点,使用合适的动物模型是必不可少的。除了最常用的啮齿类动物外,一种非人类灵长类动物——普通狨猴()在过去几年中成为一种有前景的人类衰老动物模型。然而,该物种的视觉衰老过程仅得到部分表征,尤其是在视网膜像差方面。因此,我们在此首次评估了不同年龄组普通狨猴视网膜形态的潜在变化。通过细胞类型特异性免疫标记,我们分析了不同的细胞类型和分布、潜在的光感受器和神经节细胞损失以及结构重组。我们未检测到各种细胞群体的染色模式或密度存在与年龄相关的差异迹象。例如,没有光感受器退化的迹象,并且在老年视网膜中杆双极细胞仅有极少的出芽现象。总体而言,我们在此描述了普通狨猴视网膜在衰老过程中不同细胞群体的稳定神经元结构、分布和数量得以维持,仅有轻微异常。这些发现与先前在啮齿类动物和人类中报道的结果形成鲜明对比,值得进一步研究以确定其潜在机制和可能的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e35/9479465/8ce06085cd46/fnana-16-945295-g001.jpg

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