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Immunity. 2022 Dec 13;55(12):2318-2335.e7. doi: 10.1016/j.immuni.2022.10.018. Epub 2022 Nov 14.
2
Microglia states and nomenclature: A field at its crossroads.小胶质细胞状态和命名:一个处于十字路口的领域。
Neuron. 2022 Nov 2;110(21):3458-3483. doi: 10.1016/j.neuron.2022.10.020.
3
Single cell RNA sequencing confirms retinal microglia activation associated with early onset retinal degeneration.单细胞 RNA 测序证实与早期发病的视网膜变性相关的视网膜小胶质细胞激活。
Sci Rep. 2022 Sep 10;12(1):15273. doi: 10.1038/s41598-022-19351-w.
4
Overlapping transcriptional programs promote survival and axonal regeneration of injured retinal ganglion cells.重叠的转录程序促进受损视网膜神经节细胞的存活和轴突再生。
Neuron. 2022 Aug 17;110(16):2625-2645.e7. doi: 10.1016/j.neuron.2022.06.002. Epub 2022 Jun 28.
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Neuronal apoptosis drives remodeling states of microglia and shifts in survival pathway dependence.神经元凋亡驱动小胶质细胞的重塑状态,并改变生存途径的依赖性。
Elife. 2022 Apr 28;11:e76564. doi: 10.7554/eLife.76564.
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Müller Glia maintain their regenerative potential despite degeneration in the aged zebrafish retina.Müller 胶质细胞在衰老斑马鱼视网膜退化的情况下仍保持其再生潜能。
Aging Cell. 2022 Apr;21(4):e13597. doi: 10.1111/acel.13597. Epub 2022 Mar 22.
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衰老视网膜的结构、功能和分子特征。

Structure, Function, and Molecular Landscapes of the Aging Retina.

机构信息

Department of Neuroscience, Huffington Center on Aging, Baylor College of Medicine, Houston, Texas, USA; email:

出版信息

Annu Rev Vis Sci. 2023 Sep 15;9:177-199. doi: 10.1146/annurev-vision-112122-020950. Epub 2023 May 17.

DOI:10.1146/annurev-vision-112122-020950
PMID:37196423
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10524587/
Abstract

Because the central nervous system is largely nonrenewing, neurons and their synapses must be maintained over the lifetime of an individual to ensure circuit function. Age is a dominant risk factor for neural diseases, and declines in nervous system function are a common feature of aging even in the absence of disease. These alterations extend to the visual system and, in particular, to the retina. The retina is a site of clinically relevant age-related alterations but has also proven to be a uniquely approachable system for discovering principles that govern neural aging because it is well mapped, contains diverse neuron types, and is experimentally accessible. In this article, we review the structural and molecular impacts of aging on neurons within the inner and outer retina circuits. We further discuss the contribution of non-neuronal cell types and systems to retinal aging outcomes. Understanding how and why the retina ages is critical to efforts aimed at preventing age-related neural decline and restoring neural function.

摘要

由于中枢神经系统在很大程度上不可再生,因此个体的一生都必须维持神经元及其突触,以确保电路功能。年龄是神经疾病的主要危险因素,即使在没有疾病的情况下,神经系统功能的衰退也是衰老的一个常见特征。这些改变延伸到视觉系统,特别是视网膜。视网膜是与年龄相关的临床相关改变的部位,但它也被证明是一个独特的易于接近的系统,用于发现支配神经衰老的原则,因为它具有良好的映射、包含多种神经元类型,并且具有实验可及性。在本文中,我们综述了衰老对内、外视网膜回路中神经元的结构和分子影响。我们进一步讨论了非神经元细胞类型和系统对视网膜衰老结果的贡献。了解视网膜为什么以及如何衰老对于预防与年龄相关的神经衰退和恢复神经功能的努力至关重要。