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Rare and Common Genetic Variants, Smoking, and Body Mass Index: Progression and Earlier Age of Developing Advanced Age-Related Macular Degeneration.罕见和常见的遗传变异、吸烟和体重指数:进展和更早年龄出现晚期年龄相关性黄斑变性。
Invest Ophthalmol Vis Sci. 2020 Dec 1;61(14):32. doi: 10.1167/iovs.61.14.32.
2
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration.RabGEF1 相关的内吞作用丧失导致光感受器的异常形态发生和自噬改变,从而导致视网膜变性。
PLoS Genet. 2020 Dec 23;16(12):e1009259. doi: 10.1371/journal.pgen.1009259. eCollection 2020 Dec.
3
Reprogramming to recover youthful epigenetic information and restore vision.重编程以恢复年轻的表观遗传信息并恢复视力。
Nature. 2020 Dec;588(7836):124-129. doi: 10.1038/s41586-020-2975-4. Epub 2020 Dec 2.
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Oxidative stress in the light-exposed retina and its implication in age-related macular degeneration.光暴露视网膜中的氧化应激及其在年龄相关性黄斑变性中的意义。
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Epigenetic hallmarks of age-related macular degeneration are recapitulated in a photosensitive mouse model.与年龄相关的黄斑变性的表观遗传特征在感光性小鼠模型中得到再现。
Hum Mol Genet. 2020 Aug 29;29(15):2611-2624. doi: 10.1093/hmg/ddaa158.
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Calorie Restriction and Aging in Humans.热量限制与人类衰老。
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Aging Cell. 2020 Jul;19(7):e13167. doi: 10.1111/acel.13167. Epub 2020 Jun 5.
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Trends Genet. 2020 Aug;36(8):610-623. doi: 10.1016/j.tig.2020.05.004. Epub 2020 Jun 1.
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Voluntary Exercise Suppresses Choroidal Neovascularization in Mice.自愿运动抑制了小鼠脉络膜新生血管的形成。
Invest Ophthalmol Vis Sci. 2020 May 11;61(5):52. doi: 10.1167/iovs.61.5.52.

视网膜衰老:分子和代谢紊乱及其潜在干预。

Aging of the Retina: Molecular and Metabolic Turbulences and Potential Interventions.

机构信息

Neurobiology, Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA; email:

出版信息

Annu Rev Vis Sci. 2021 Sep 15;7:633-664. doi: 10.1146/annurev-vision-100419-114940. Epub 2021 Jun 1.

DOI:10.1146/annurev-vision-100419-114940
PMID:34061570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11375453/
Abstract

Multifaceted and divergent manifestations across tissues and cell types have curtailed advances in deciphering the cellular events that accompany advanced age and contribute to morbidities and mortalities. Increase in human lifespan during the past century has heightened awareness of the need to prevent age-associated frailty of neuronal and sensory systems to allow a healthy and productive life. In this review, we discuss molecular and physiological attributes of aging of the retina, with a goal of understanding age-related impairment of visual function. We highlight the epigenome-metabolism nexus and proteostasis as key contributors to retinal aging and discuss lifestyle changes as potential modulators of retinal function. Finally, we deliberate promising intervention strategies for promoting healthy aging of the retina for improved vision.

摘要

多方面和多样化的组织和细胞类型的表现,阻碍了对伴随衰老的细胞事件的破译,这些事件导致了发病率和死亡率的增加。在过去的一个世纪中,人类寿命的延长提高了人们对预防与年龄相关的神经元和感觉系统衰弱的认识,以实现健康和富有成效的生活。在这篇综述中,我们讨论了视网膜衰老的分子和生理特征,旨在了解与年龄相关的视觉功能障碍。我们强调了表观基因组-代谢关联和蛋白质稳态作为导致视网膜衰老的关键因素,并讨论了生活方式的改变作为视网膜功能的潜在调节剂。最后,我们审议了促进视网膜健康衰老以改善视力的有前途的干预策略。