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研究细胞内神经毒性蛋白聚集体的结构。

Investigating the Structure of Neurotoxic Protein Aggregates Inside Cells.

机构信息

Max-Planck-Institute of Biochemistry, Department for Molecular Structural Biology, Am Klopferspitz 18, 82152 Planegg, Germany.

Max-Planck-Institute of Biochemistry, Department for Molecular Structural Biology, Am Klopferspitz 18, 82152 Planegg, Germany; University Medical Center Göttingen, Institute for Neuropathology, Robert-Koch-Strasse 40, 37075 Göttingen, Germany; Cluster of Excellence 'Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells' (MBExC), University of Göttingen, Göttingen, Germany.

出版信息

Trends Cell Biol. 2020 Dec;30(12):951-966. doi: 10.1016/j.tcb.2020.08.007. Epub 2020 Sep 24.

Abstract

Neurodegenerative diseases affect the lives of millions of people across the world, being particularly prevalent in the aging population. Despite huge research efforts, conclusive insights into the disease mechanisms are still lacking. Therefore, therapeutic strategies are limited to symptomatic treatments. A common histopathological hallmark of many neurodegenerative diseases is the presence of large pathognomonic protein aggregates, but their role in the disease pathology is unclear and subject to controversy. Here, we discuss imaging methods allowing investigation of these structures within their cellular environment: conventional electron microscopy (EM), super-resolution light microscopy (SR-LM), and cryo-electron tomography (cryo-ET). Multidisciplinary approaches are key for understanding neurodegenerative diseases and may contribute to the development of effective treatments. For simplicity, we focus on huntingtin aggregates, characteristic of Huntington's disease.

摘要

神经退行性疾病影响着全球数百万人的生活,在老年人群中尤为普遍。尽管进行了大量的研究,但对疾病机制仍缺乏明确的认识。因此,治疗策略仅限于对症治疗。许多神经退行性疾病的一个常见组织病理学特征是存在大型特征性蛋白聚集体,但它们在疾病发病机制中的作用尚不清楚,存在争议。在这里,我们讨论了允许在细胞环境中研究这些结构的成像方法:常规电子显微镜(EM)、超分辨率光学显微镜(SR-LM)和冷冻电子断层扫描(cryo-ET)。多学科方法是理解神经退行性疾病的关键,可能有助于开发有效的治疗方法。为简单起见,我们重点讨论亨廷顿病特征性的亨廷顿蛋白聚集体。

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