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路易体痴呆患者额叶皮质脂筏中脂质谱和蛋白质分布出现的异常揭示了阿尔茨海默病和帕金森病部分共有的神经化学特征。

Anomalies occurring in lipid profiles and protein distribution in frontal cortex lipid rafts in dementia with Lewy bodies disclose neurochemical traits partially shared by Alzheimer's and Parkinson's diseases.

作者信息

Marin Raquel, Fabelo Noemí, Martín Virginia, Garcia-Esparcia Paula, Ferrer Isidre, Quinto-Alemany David, Díaz Mario

机构信息

Departamento de Fisiología, Universidad de La Laguna, Tenerife, Spain.

Departamento de Biología Animal, Universidad de La Laguna, Tenerife, Spain.

出版信息

Neurobiol Aging. 2017 Jan;49:52-59. doi: 10.1016/j.neurobiolaging.2016.08.027. Epub 2016 Sep 6.

Abstract

Lipid rafts are highly dynamic membrane microdomains intimately associated with cell signaling. Compelling evidence has demonstrated that alterations in lipid rafts are associated with neurodegenerative diseases such Alzheimer's disease, but at present, whether alterations in lipid raft microdomains occur in other types of dementia such dementia with Lewy bodies (DLB) remains unknown. Our analyses reveal that lipid rafts from DLB exhibit aberrant lipid profiles including low levels of n-3 long-chain polyunsaturated fatty acids (mainly docosahexaenoic acid), plasmalogens and cholesterol, and reduced unsaturation and peroxidability indexes. As a consequence, lipid raft resident proteins holding principal factors of the β-amyloidogenic pathway, including β-amyloid precursor protein, presenilin 1, β-secretase, and PrP, are redistributed between lipid rafts and nonraft domains in DLB frontal cortex. Meta-analysis discloses certain similarities in the altered composition of lipid rafts between DLB and Parkinson's disease which are in line with the spectrum of Lewy body diseases. In addition, redistribution of proteins linked to the β-amyloidogenic pathway in DLB can facilitate generation of β-amyloid, thus providing mechanistic clues to the intriguing convergence of Alzheimer's disease pathology, particularly β-amyloid deposition, in DLB.

摘要

脂筏是与细胞信号传导密切相关的高度动态的膜微区。有力证据表明,脂筏的改变与神经退行性疾病如阿尔茨海默病有关,但目前,脂筏微区的改变是否发生在其他类型的痴呆如路易体痴呆(DLB)中仍不清楚。我们的分析表明,DLB的脂筏呈现异常的脂质谱,包括低水平的n-3长链多不饱和脂肪酸(主要是二十二碳六烯酸)、缩醛磷脂和胆固醇,以及降低的不饱和度和过氧化性指数。因此,在DLB额叶皮质中,包含β淀粉样蛋白生成途径主要因子的脂筏驻留蛋白,包括β淀粉样前体蛋白、早老素1、β分泌酶和朊蛋白,在脂筏和非脂筏结构域之间重新分布。荟萃分析揭示了DLB和帕金森病在脂筏组成改变方面存在某些相似之处,这与路易体病谱一致。此外,DLB中与β淀粉样蛋白生成途径相关的蛋白质重新分布可促进β淀粉样蛋白的产生,从而为DLB中阿尔茨海默病病理,特别是β淀粉样蛋白沉积的有趣趋同提供了机制线索。

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