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α-突触核蛋白聚集的中间体:对帕金森病发病机制的影响。

Intermediates of α-synuclein aggregation: Implications in Parkinson's disease pathogenesis.

作者信息

Gadhe Laxmikant, Sakunthala Arunima, Mukherjee Semanti, Gahlot Nitisha, Bera Riya, Sawner Ajay Singh, Kadu Pradeep, Maji Samir K

机构信息

Department of Biosciences and Bioengineering, IIT Bombay, Powai, Mumbai 400076, India.

Department of Biosciences and Bioengineering, IIT Bombay, Powai, Mumbai 400076, India.

出版信息

Biophys Chem. 2022 Feb;281:106736. doi: 10.1016/j.bpc.2021.106736. Epub 2021 Dec 6.

Abstract

Cytoplasmic deposition of aberrantly misfolded α-synuclein (α-Syn) is a common feature of synucleinopathies, including Parkinson's disease (PD). However, the precise pathogenic mechanism of α-Syn in synucleinopathies remains elusive. Emerging evidence has suggested that α-Syn may contribute to PD pathogenesis in several ways; wherein the contribution of fibrillar species, for exerting toxicity and disease transmission, cannot be neglected. Further, the oligomeric species could be the most plausible neurotoxic species causing neuronal cell death. However, understanding the structural and molecular insights of these oligomers are very challenging due to the heterogeneity and transient nature of the species. In this review, we discuss the recent advancements in understanding the formation and role of α-Syn oligomers in PD pathogenesis. We also summarize the different types of α-Syn oligomeric species and potential mechanisms to exert neurotoxicity. Finally, we address the possible ways to target α-Syn as a promising approach against PD and the possible future directions.

摘要

异常错误折叠的α-突触核蛋白(α-Syn)在细胞质中的沉积是突触核蛋白病(包括帕金森病(PD))的一个共同特征。然而,α-Syn在突触核蛋白病中的精确致病机制仍不清楚。新出现的证据表明,α-Syn可能通过多种方式导致PD发病;其中,纤维状物种在发挥毒性和疾病传播方面的作用不可忽视。此外,寡聚体物种可能是导致神经元细胞死亡的最合理的神经毒性物种。然而,由于这些物种的异质性和短暂性,了解这些寡聚体的结构和分子见解极具挑战性。在这篇综述中,我们讨论了在理解α-Syn寡聚体在PD发病机制中的形成和作用方面的最新进展。我们还总结了不同类型的α-Syn寡聚体物种以及发挥神经毒性的潜在机制。最后,我们探讨了将α-Syn作为对抗PD的一种有前景的方法的可能途径以及未来可能的方向。

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