加齢によるシナプスタンパク質分解低下と疾患リスク(Aging slows breakdown of synaptic proteins, raising disease risk)

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2026-02-02 スタンフォード大学

スタンフォード大学の研究チームは、加齢に伴う認知機能低下やアルツハイマー病に関与する脳内タンパク質の変化を詳細に解析した。研究では、高齢脳において特定のタンパク質が異常に蓄積または減少することで、神経細胞間の情報伝達や可塑性が損なわれ、記憶や判断力の低下につながることが示された。特に、アルツハイマー病患者の脳では、加齢による変化がさらに増幅され、病的なタンパク質ネットワークが形成されることが確認された。この成果は、正常老化と疾患による変化を区別する手がかりを提供し、早期診断マーカーの開発や、加齢脳を標的とした新たな治療法設計につながる可能性を示している。

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老化はミクログリア細胞における分解の遅いシナプスタンパク質の蓄積を促進する Ageing promotes microglial accumulation of slow-degrading synaptic proteins

Ian H. Guldner,Viktoria P. Wagner,Patricia Moran-Losada,Sophia M. Shi,Sophia W. Golub,Johannes F. Hevler,Kelly Chen,Barbara T. Meese,Ali Ghoochani,Ernst Pulido,Hamilton Se-Hwee Oh,Yann Le Guen,Nannan Lu,Pui Shuen Wong,Ning-Sum To,Dylan Garceau,Zimin Guo,Jian Luo,Carolyn R. Bertozzi,Emma Lundberg,Monther Abu-Remaileh,Michael Sasner,Andreas Keller,Andrew C. Yang,… Tony Wyss-Coray
Nature  Published:21 January 2026
DOI:https://doi.org/10.1038/s41586-025-09987-9

加齢によるシナプスタンパク質分解低下と疾患リスク(Aging slows breakdown of synaptic proteins, raising disease risk)

Abstract

Neurodegenerative diseases affect 1 in 12 people globally and remain incurable. Central to their pathogenesis is a loss of neuronal protein maintenance and the accumulation of protein aggregates with ageing1,2. Here we engineered bioorthogonal tools3 that enabled us to tag the nascent neuronal proteome and study its turnover with ageing, its propensity to aggregate and its interaction with microglia. We show that neuronal protein half-life approximately doubles on average between 4-month-old and 24-month-old mice, with the stability of individual proteins differing among brain regions. Furthermore, we describe the aged neuronal ‘aggregome’, which encompasses 1,726 proteins, nearly half of which show reduced degradation with age. The aggregome includes well-known proteins linked to diseases and numerous proteins previously not associated with neurodegeneration. Notably, we demonstrate that neuronal proteins accumulate in aged microglia, with 54% also displaying reduced degradation and/or aggregation with age. Among these proteins, synaptic proteins are highly enriched, which suggests that there is a cascade of events that emerge from impaired synaptic protein turnover and aggregation to the disposal of these proteins, possibly through microglial engulfment of synapses. These findings reveal the substantial loss of neuronal proteome maintenance with ageing, which could be causal for age-related synapse loss and cognitive decline.

医療・健康
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