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针对tau蛋白病和年龄相关性黄斑变性的共同通路:对新型疗法的启示。

Targeting shared pathways in tauopathies and age-related macular degeneration: implications for novel therapies.

作者信息

Rinaldi Michele, Pezone Antonio, Quadrini Gaia Italia, Abbadessa Gianmarco, Laezza Maria Paola, Passaro Maria Laura, Porcellini Antonio, Costagliola Ciro

机构信息

Department of Neurosciences, Reproductive Sciences and Dentistry, University of Naples Federico II, Naples, Italy.

Department of Biology, University of Naples Federico II, Naples, Italy.

出版信息

Front Aging Neurosci. 2024 Apr 3;16:1371745. doi: 10.3389/fnagi.2024.1371745. eCollection 2024.

Abstract

The intricate parallels in structure and function between the human retina and the central nervous system designate the retina as a prospective avenue for understanding brain-related processes. This review extensively explores the shared physiopathological mechanisms connecting age-related macular degeneration (AMD) and proteinopathies, with a specific focus on tauopathies. The pivotal involvement of oxidative stress and cellular senescence emerges as key drivers of pathogenesis in both conditions. Uncovering these shared elements not only has the potential to enhance our understanding of intricate neurodegenerative diseases but also sets the stage for pioneering therapeutic approaches in AMD.

摘要

人类视网膜与中枢神经系统在结构和功能上的复杂相似之处,表明视网膜是理解大脑相关过程的一个有前景的途径。本综述广泛探讨了与年龄相关性黄斑变性(AMD)和蛋白病相关的共同病理生理机制,特别关注tau蛋白病。氧化应激和细胞衰老的关键作用成为这两种疾病发病机制的关键驱动因素。揭示这些共同因素不仅有可能加深我们对复杂神经退行性疾病的理解,也为AMD的开创性治疗方法奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/11021713/1fbbac21af6c/fnagi-16-1371745-g001.jpg

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