利用α-klotho的神经保护作用来解决衰老和神经退行性相关的认知功能障碍。

Q4 Neuroscience Neuronal signaling Pub Date : 2021-06-14 eCollection Date: 2021-06-01 DOI:10.1042/NS20200101
Kelsey Hanson, Kate Fisher, Nigel M Hooper
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引用次数: 10

摘要

认知功能障碍是衰老和神经退行性疾病(如阿尔茨海默病)的主要症状。提高认识的战略将影响很大一部分老龄人口的生活质量。α-klotho蛋白可以通过多种机制防止认知能力下降:例如通过激活N-甲基-d-天冬氨酸(NMDA)受体信号来促进最佳突触功能;刺激抗氧化防御系统;减少炎症;促进自噬和提高淀粉样蛋白-β的清除率。然而,α-klotho介导这些神经保护功能的分子和细胞途径尚未完全阐明。关键问题仍未得到解答:哪种形式的α-klotho(跨膜、可溶性或分泌型)介导其认知增强特性;α-klotho的神经元受体是什么?大脑中哪些信号通路被α-kloto激活以增强认知;外周给药的α-克洛托如何介导神经保护作用;α-克洛托的VS变体的有益作用的分子基础是什么?在这篇综述中,我们总结了最近对神经元α-klotho的研究,并讨论了如何利用α-kloto的神经保护特性来解决与年龄和神经退行性变相关的认知功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Exploiting the neuroprotective effects of α-klotho to tackle ageing- and neurodegeneration-related cognitive dysfunction.

Cognitive dysfunction is a key symptom of ageing and neurodegenerative disorders, such as Alzheimer's disease (AD). Strategies to enhance cognition would impact the quality of life for a significant proportion of the ageing population. The α-klotho protein may protect against cognitive decline through multiple mechanisms: such as promoting optimal synaptic function via activation of N-methyl-d-aspartate (NMDA) receptor signalling; stimulating the antioxidant defence system; reducing inflammation; promoting autophagy and enhancing clearance of amyloid-β. However, the molecular and cellular pathways by which α-klotho mediates these neuroprotective functions have yet to be fully elucidated. Key questions remain unanswered: which form of α-klotho (transmembrane, soluble or secreted) mediates its cognitive enhancing properties; what is the neuronal receptor for α-klotho and which signalling pathways are activated by α-klotho in the brain to enhance cognition; how does peripherally administered α-klotho mediate neuroprotection; and what is the molecular basis for the beneficial effect of the VS variant of α-klotho? In this review, we summarise the recent research on neuronal α-klotho and discuss how the neuroprotective properties of α-klotho could be exploited to tackle age- and neurodegeneration-associated cognitive dysfunction.

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来源期刊
CiteScore
4.60
自引率
0.00%
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审稿时长
14 weeks
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