神经退行性疾病病理蛋白扩散的基于连接体的生物物理模型。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-01-21 eCollection Date: 2025-01-01 DOI:10.1371/journal.pcbi.1012743
Peng Ren, Xuehua Cui, Xia Liang
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引用次数: 0

摘要

神经退行性疾病是一组以神经元进行性变性或死亡为特征的疾病。临床症状的复杂性和疾病进展的不可逆性显著影响个体生命,导致过早死亡。神经退行性疾病的患病率不断上升,但具体的发病机制仍不完全清楚,缺乏有效的治疗策略。近年来,越来越多的实验证据支持“朊病毒样传播”假设,即异常蛋白诱导正常蛋白错误折叠,这些错误折叠的蛋白在整个神经网络中传播,导致神经元死亡。为了从计算角度阐明这一动态过程,研究人员提出了三种基于连接体的生物物理模型来模拟病理蛋白的传播:网络扩散模型、流行病传播模型和基于agent的易感-传染性-去除模型。这些模型已经证明了有前景的预测能力。本文着重介绍了它们的基本原理和应用。然后,我们比较了模型的优缺点。在此基础上,我们引入了模型优化的新方向,并提出了一个统一的基于连接体的生物物理模型评估框架。我们期望本文的综述能够降低该领域研究人员的进入门槛,加速模型优化,从而促进基于连接体的生物物理模型的临床转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Connectome-based biophysical models of pathological protein spreading in neurodegenerative diseases.

Neurodegenerative diseases are a group of disorders characterized by progressive degeneration or death of neurons. The complexity of clinical symptoms and irreversibility of disease progression significantly affects individual lives, leading to premature mortality. The prevalence of neurodegenerative diseases keeps increasing, yet the specific pathogenic mechanisms remain incompletely understood and effective treatment strategies are lacking. In recent years, convergent experimental evidence supports the "prion-like transmission" assumption that abnormal proteins induce misfolding of normal proteins, and these misfolded proteins propagate throughout the neural networks to cause neuronal death. To elucidate this dynamic process in vivo from a computational perspective, researchers have proposed three connectome-based biophysical models to simulate the spread of pathological proteins: the Network Diffusion Model, the Epidemic Spreading Model, and the agent-based Susceptible-Infectious-Removed model. These models have demonstrated promising predictive capabilities. This review focuses on the explanations of their fundamental principles and applications. Then, we compare the strengths and weaknesses of the models. Building upon this foundation, we introduce new directions for model optimization and propose a unified framework for the evaluation of connectome-based biophysical models. We expect that this review could lower the entry barrier for researchers in this field, accelerate model optimization, and thereby advance the clinical translation of connectome-based biophysical models.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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