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生活方式在营养感应途径对认知老化的作用中起中介作用:细胞和流行病学证据。

Lifestyle mediates the role of nutrient-sensing pathways in cognitive aging: cellular and epidemiological evidence.

机构信息

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.

出版信息

Commun Biol. 2020 Apr 2;3(1):157. doi: 10.1038/s42003-020-0844-1.

Abstract

Aging induces cellular and molecular changes including modification of stem cell pools. In particular, alterations in aging neural stem cells (NSCs) are linked to age-related cognitive decline which can be modulated by lifestyle. Nutrient-sensing pathways provide a molecular basis for the link between lifestyle and cognitive decline. Adopting a back-translation strategy using stem cell biology to inform epidemiological analyses, here we show associations between cellular readouts of NSC maintenance and expression levels of nutrient-sensing genes following NSC exposure to aging human serum as well as morphological and gene expression alterations following repeated passaging. Epidemiological analyses on the identified genes showed associations between polymorphisms in SIRT1 and ABTB1 and cognitive performance as well as interactions between SIRT1 genotype and physical activity and between GRB10 genotype and adherence to a Mediterranean diet. Our study contributes to the understanding of neural stem cell molecular mechanisms underlying human cognitive aging and hints at lifestyle modifiable factors.

摘要

衰老是诱导细胞和分子变化的原因,包括干细胞池的改变。特别是,衰老神经干细胞(NSC)的改变与年龄相关的认知能力下降有关,而生活方式可以调节这种改变。营养感应途径为生活方式与认知能力下降之间的联系提供了分子基础。我们采用反向翻译策略,利用干细胞生物学为流行病学分析提供信息,结果表明,在 NSC 暴露于老化的人血清后,NSC 维持的细胞读数与营养感应基因的表达水平之间存在关联,并且在重复传代后会出现形态和基因表达改变。对鉴定出的基因进行的流行病学分析表明,SIRT1 和 ABTB1 中的多态性与认知表现有关,SIRT1 基因型与体力活动之间以及 GRB10 基因型与地中海饮食的依从性之间存在相互作用。我们的研究有助于理解人类认知衰老的神经干细胞分子机制,并暗示了可通过生活方式改变的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e18/7118127/7f72a9415d34/42003_2020_844_Fig1_HTML.jpg

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