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他汀类药物通过降低胆固醇抑制α-突触核蛋白的细胞间传播。

Statins suppress cell-to-cell propagation of α-synuclein by lowering cholesterol.

机构信息

Department of Biomedical Sciences, Neuroscience Research Institute, Convergence Research Center for Dementia, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.

Interdisciplinary Program in Neuroscience, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea.

出版信息

Cell Death Dis. 2023 Jul 27;14(7):474. doi: 10.1038/s41419-023-05977-9.

Abstract

Cell-to-cell propagation of protein aggregates has been implicated in the progression of neurodegenerative diseases. However, the underlying mechanism and modulators of this process are not fully understood. Here, we screened a small-molecule library in a search for agents that suppress the propagation of α-synuclein and mutant huntingtin (mHtt). These screens yielded several molecules, some of which were effective against both α-synuclein and mHtt. Among these molecules, we focused on simvastatin and pravastatin. Simvastatin administration in a transgenic model of synucleinopathy effectively ameliorated behavioral deficits and α-synuclein accumulation, whereas pravastatin had no effect. Because only simvastatin enters the brain effectively, these results suggest that inhibition of brain cholesterol synthesis is important in simvastatin effects. In cultured cells, accumulation of intracellular cholesterol, induced by genetic ablation of the NPC1 gene or by pharmacological treatment with U18666A, increased α-synuclein aggregation and secretion. In contrast, lowering cholesterol using methyl-β-cyclodextrin or statins reversed α-synuclein aggregation and secretion in NPC1-knockout cells. Consistent with these observations, feeding a high-fat diet aggravated α-synuclein pathology and behavioral deficits in the preformed fibril-injected mouse model, an effect that was also reversed by simvastatin administration. These results suggest that statins suppress propagation of protein aggregates by lowering cholesterol in the brain.

摘要

细胞间蛋白质聚集物的传播被认为与神经退行性疾病的进展有关。然而,该过程的潜在机制和调节剂尚未完全了解。在这里,我们在小分子文库中进行筛选,寻找抑制α-突触核蛋白和突变型亨廷顿蛋白(mHtt)传播的药物。这些筛选产生了几种分子,其中一些对α-突触核蛋白和 mHtt 都有效。在这些分子中,我们重点研究了辛伐他汀和普伐他汀。在突触核蛋白病的转基因模型中,辛伐他汀的给药有效地改善了行为缺陷和α-突触核蛋白的积累,而普伐他汀则没有效果。由于只有辛伐他汀能有效地进入大脑,这些结果表明抑制脑胆固醇合成对辛伐他汀的作用很重要。在培养的细胞中,通过 NPC1 基因的遗传缺失或用 U18666A 进行药物处理诱导细胞内胆固醇积累,增加了α-突触核蛋白的聚集和分泌。相比之下,使用甲基-β-环糊精或他汀类药物降低胆固醇可逆转 NPC1 敲除细胞中的α-突触核蛋白聚集和分泌。与这些观察结果一致,高脂饮食加重了预形成纤维注射小鼠模型中的α-突触核蛋白病理和行为缺陷,而辛伐他汀的给药也逆转了这种作用。这些结果表明,他汀类药物通过降低大脑中的胆固醇来抑制蛋白质聚集物的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5c/10374525/9bd35a8e94c5/41419_2023_5977_Fig1_HTML.jpg

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