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淀粉样β单体对脂膜力学参数的影响——对阿尔茨海默病中机械驱动神经退行性变的潜在影响。

Effect of Amyloid-β Monomers on Lipid Membrane Mechanical Parameters-Potential Implications for Mechanically Driven Neurodegeneration in Alzheimer's Disease.

机构信息

Laboratory of Cytobiochemistry, Faculty of Biotechnology, University of Wrocław, F. Joliot-Curie 14a, 50-383 Wrocław, Poland.

Łukasiewicz Research Network-PORT Polish Center for Technology Development, Stabłowicka 147, 54-066 Wrocław, Poland.

出版信息

Int J Mol Sci. 2020 Dec 22;22(1):18. doi: 10.3390/ijms22010018.

DOI:10.3390/ijms22010018
PMID:33375009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7792773/
Abstract

Alzheimer's disease (AD) is a neurodegenerative disease that results in memory loss and the impairment of cognitive skills. Several mechanisms of AD's pathogenesis were proposed, such as the progressive accumulation of amyloid-β (Aβ) and τ pathology. Nevertheless, the exact neurodegenerative mechanism of the Aβ remains complex and not fully understood. This paper proposes an alternative hypothesis of the mechanism based on maintaining the neuron membrane's mechanical balance. The incorporation of Aβ decreases the lipid membrane's elastic properties, which eventually leads to the impairment of membrane clustering, disruption of mechanical wave propagation, and change in gamma oscillations. The first two disrupt the neuron's ability to function correctly while the last one decreases sensory encoding and perception enabling. To begin discussing this mechanical-balance hypothesis, we measured the effect of two selected peptides, Aβ-40 and Aβ-42, as well as their fluorescently labeled modification, on membrane mechanical properties. The decrease of bending rigidity, consistent for all investigated peptides, was observed using molecular dynamic studies and experimental flicker-noise techniques. Additionally, wave propagation was investigated with molecular dynamic studies in membranes with and without incorporated neurodegenerative peptides. A change in membrane behavior was observed in the membrane system with incorporated Aβ.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,导致记忆丧失和认知能力受损。已经提出了几种 AD 发病机制的机制,例如淀粉样蛋白-β(Aβ)和τ病理学的渐进积累。然而,Aβ 的确切神经退行性机制仍然很复杂,尚未完全理解。本文基于维持神经元膜的机械平衡提出了一种替代机制假设。Aβ 的掺入降低了脂质膜的弹性特性,最终导致膜聚类受损、机械波传播中断以及γ振荡的改变。前两个破坏了神经元正常运作的能力,而最后一个降低了感觉编码和感知能力。为了开始讨论这种机械平衡假说,我们测量了两种选定的肽(Aβ-40 和 Aβ-42)及其荧光标记修饰对膜机械性能的影响。使用分子动力学研究和实验闪烁噪声技术观察到所有研究肽的弯曲刚性降低。此外,还使用分子动力学研究在有和没有掺入神经退行性肽的膜中研究了波传播。在含有 Aβ 的膜系统中观察到膜行为的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/62437e096ae2/ijms-22-00018-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/e8e0d509fe7a/ijms-22-00018-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/61d98ec28270/ijms-22-00018-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/a6287566dd09/ijms-22-00018-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/ff946f125621/ijms-22-00018-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/62437e096ae2/ijms-22-00018-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/e8e0d509fe7a/ijms-22-00018-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/61d98ec28270/ijms-22-00018-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/a6287566dd09/ijms-22-00018-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/ff946f125621/ijms-22-00018-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/7792773/62437e096ae2/ijms-22-00018-g005.jpg

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