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神经退行性疾病中选择性脆弱性的分子和细胞机制。

Molecular and cellular mechanisms of selective vulnerability in neurodegenerative diseases.

机构信息

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA, USA.

Institute for Neurodegenerative Diseases, University of California, San Francisco, San Francisco, CA, USA.

出版信息

Nat Rev Neurosci. 2024 May;25(5):351-371. doi: 10.1038/s41583-024-00806-0. Epub 2024 Apr 4.

Abstract

The selective vulnerability of specific neuronal subtypes is a hallmark of neurodegenerative diseases. In this Review, I summarize our current understanding of the brain regions and cell types that are selectively vulnerable in different neurodegenerative diseases and describe the proposed underlying cell-autonomous and non-cell-autonomous mechanisms. I highlight how recent methodological innovations - including single-cell transcriptomics, CRISPR-based screens and human cell-based models of disease - are enabling new breakthroughs in our understanding of selective vulnerability. An understanding of the molecular mechanisms that determine selective vulnerability and resilience would shed light on the key processes that drive neurodegeneration and point to potential therapeutic strategies to protect vulnerable cell populations.

摘要

特定神经元亚型的选择性易损性是神经退行性疾病的一个标志。在这篇综述中,我总结了我们目前对不同神经退行性疾病中选择性易损的脑区和细胞类型的理解,并描述了所提出的潜在的细胞自主和非细胞自主机制。我强调了最近的方法创新,包括单细胞转录组学、基于 CRISPR 的筛选和基于人类细胞的疾病模型,如何使我们对选择性易损性的理解取得新的突破。对决定选择性易损性和弹性的分子机制的理解将揭示驱动神经退行性变的关键过程,并为保护易损细胞群体指出潜在的治疗策略。

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