Department of Neuroscience, Huffington Center on Aging, Baylor College of Medicine, Houston, Texas, USA; email:
Annu Rev Vis Sci. 2023 Sep 15;9:177-199. doi: 10.1146/annurev-vision-112122-020950. Epub 2023 May 17.
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.
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。