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Targeting Liquid-Liquid Phase Separation and Autophagy in Alzheimer's Disease: Insights into Molecular Mechanisms and Therapeutic Potential.

Xiaopeng Li, Yan Liu, Hong Hu, Shenghong Li
Review Neurochemical research 2025
PubMed DOI
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Study Design

研究タイプ
Review
対象集団
Alzheimer's disease (review of mechanisms)
介入
Targeting Liquid-Liquid Phase Separation and Autophagy in Alzheimer's Disease: Insights into Molecular Mechanisms and Therapeutic Potential. None
比較対照
None
主要アウトカム
AD pathology modulation via LLPS and autophagy
効果の方向
Positive
バイアスリスク
Unclear

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the leading cause of dementia, marked by cognitive decline and memory loss. Its multifactorial etiology involves genetic, environmental, and cellular factors, with key pathological features including amyloid-beta (Aβ) plaques and tau tangles. Recent studies have highlighted the roles of liquid-liquid phase separation (LLPS) and autophagy in AD onset and progression. LLPS, an emerging biophysical phenomenon, facilitates protein aggregation and may contribute to early disease stages. Dysregulated autophagy results in the accumulation of toxic proteins, such as Aβ and tau, exacerbating neurodegeneration. This review explores the interplay between LLPS and autophagy in AD, a relationship often overlooked in the literature. It examines their biological mechanisms, synergistic effects on AD pathology, and potential therapeutic strategies. Additionally, we discuss the therapeutic potential of both natural and non-natural compounds in modulating LLPS and autophagy. While compounds like curcumin show promise, a comprehensive framework for their targeted use remains under development. This review provides theoretical support for the advancement of more precise AD therapies.

要約

A review of the interplay between LLPS and autophagy in AD examines their biological mechanisms, synergistic effects on AD pathology, and potential therapeutic strategies and provides theoretical support for the advancement of more precise AD therapies.

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