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tau 病和突触核蛋白病之间的重叠和分歧:神经退行性变的二重奏。

Overlaps and divergences between tauopathies and synucleinopathies: a duet of neurodegeneration.

机构信息

Health Sciences Institute, Key Laboratory of Major Chronic Diseases of Nervous System of Liaoning Province, China Medical University, Shenyang, 110122, China.

Neural Plasticity and Repair Unit, Department of Experimental Medical Science, Wallenberg Neuroscience Center, Lund University, BMC A10, 22184, Lund, Sweden.

出版信息

Transl Neurodegener. 2024 Mar 26;13(1):16. doi: 10.1186/s40035-024-00407-y.

Abstract

Proteinopathy, defined as the abnormal accumulation of proteins that eventually leads to cell death, is one of the most significant pathological features of neurodegenerative diseases. Tauopathies, represented by Alzheimer's disease (AD), and synucleinopathies, represented by Parkinson's disease (PD), show similarities in multiple aspects. AD manifests extrapyramidal symptoms while dementia is also a major sign of advanced PD. We and other researchers have sequentially shown the cross-seeding phenomenon of α-synuclein (α-syn) and tau, reinforcing pathologies between synucleinopathies and tauopathies. The highly overlapping clinical and pathological features imply shared pathogenic mechanisms between the two groups of disease. The diagnostic and therapeutic strategies seemingly appropriate for one distinct neurodegenerative disease may also apply to a broader spectrum. Therefore, a clear understanding of the overlaps and divergences between tauopathy and synucleinopathy is critical for unraveling the nature of the complicated associations among neurodegenerative diseases. In this review, we discuss the shared and diverse characteristics of tauopathies and synucleinopathies from aspects of genetic causes, clinical manifestations, pathological progression and potential common therapeutic approaches targeting the pathology, in the aim to provide a timely update for setting the scheme of disease classification and provide novel insights into the therapeutic development for neurodegenerative diseases.

摘要

蛋白病,定义为蛋白质的异常积累,最终导致细胞死亡,是神经退行性疾病的最重要的病理特征之一。以阿尔茨海默病(AD)为代表的tau 病和以帕金森病(PD)为代表的突触核蛋白病在多个方面表现出相似性。AD 表现出锥体外系症状,而痴呆也是 PD 晚期的主要标志。我们和其他研究人员已经相继展示了α-突触核蛋白(α-syn)和 tau 的交叉接种现象,加强了突触核蛋白病和 tau 病之间的病理学联系。高度重叠的临床和病理特征意味着这两组疾病具有共同的致病机制。针对一种特定神经退行性疾病的诊断和治疗策略似乎也适用于更广泛的范围。因此,清楚地了解 tau 病和突触核蛋白病之间的重叠和差异对于揭示神经退行性疾病之间复杂关联的本质至关重要。在这篇综述中,我们从遗传原因、临床表现、病理进展和针对病理的潜在共同治疗方法等方面讨论了 tau 病和突触核蛋白病的共同和不同特征,旨在为疾病分类方案的制定提供及时的更新,并为神经退行性疾病的治疗发展提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7578/10964635/9efa6af6f703/40035_2024_407_Fig1_HTML.jpg

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