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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Structural membrane alterations in Alzheimer brains found to be associated with regional disease development; increased density of gangliosides GM1 and GM2 and loss of cholesterol in detergent-resistant membrane domains.
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Structural membrane alterations in Alzheimer brains found to be associated with regional disease development; increased density of gangliosides GM1 and GM2 and loss of cholesterol in detergent-resistant membrane domains.

机译:发现阿尔茨海默氏症大脑中的结构性膜改变与局部疾病的发展有关;神经节苷脂GM1和GM2的密度增加,并且在耐洗涤剂的膜结构域中胆固醇的损失。

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Abstract The formation of neurotoxic beta-amyloid fibrils in Alzheimer's disease (AD) is suggested to involve membrane rafts and to be promoted, in vitro, by enriched concentrations of gangliosides, particularly GM1, and the cholesterol therein. In our study, the presence of rafts and their content of the major membrane lipids and gangliosides in the temporal cortex, reflecting late stages of AD pathology, and the frontal cortex, presenting earlier stages, has been investigated. Whole tissue and isolated detergent-resistant membrane fractions (DRMs) were analysed from 10 AD and 10 age-matched control autopsy brains. DRMs from the frontal cortex of AD brains contained a significantly higher concentration (micromol/micromol glycerophospholipids), of ganglioside GM1 (22.3 +/- 4.6 compared to 10.3 +/- 6.4, p < 0.001) and GM2 (2.5 +/- 1.0 compared to 0.55 +/- 0.3, p < 0.001). Similar increases of these gangliosides were also seen in DRMs from the temporal cortex of AD brains, which, in addition, comprised significantly lower proportions of DRMs. Moreover, these remaining rafts were depleted in cholesterol (from 1.5 +/- 0.2 to 0.6 +/- 0.3 micromol/micromol glycerophospholipids, p < 0.001). In summary, we found an increased proportion of GM1 and GM2 in DRMs, and accelerating plaque formation at an early stage, which may gradually lead to membrane raft disruptions and thereby affect cellular functions associated with the presence of such membrane domains.
机译:摘要提示阿尔茨海默氏病(AD)中神经毒性β-淀粉样蛋白原纤维的形成涉及膜筏,并且在体外可通过浓缩神经节苷脂(尤其是GM1)及其中的胆固醇来促进。在我们的研究中,已经研究了颞皮质中筏的存在及其主要膜脂和神经节苷脂的含量,反映了AD病理的晚期,而额叶皮质则处于早期。从10个AD和10个年龄匹配的对照尸检大脑中分析了整个组织和分离的耐去污剂的膜级分(DRM)。来自AD大脑额叶皮层的DRM的神经节苷脂GM1(22.3 +/- 4.6与10.3 +/- 6.4相比,p <0.001)和GM2(2.5 +/- 1.0相比)的浓度(微摩尔/微摩尔甘油磷脂)高得多至0.55 +/- 0.3,p <0.001)。在来自AD大脑颞叶皮质的DRM中也观察到了这些神经节苷脂的类似增加,此外,DRM的比例明显更低。此外,这些剩余的木筏中的胆固醇水平降低(从1.5 +/- 0.2至0.6 +/- 0.3 micromol / micromol甘油磷脂,p <0.001)。总之,我们发现DRM中GM1和GM2的比例增加,并在早期加速噬菌斑形成,这可能会逐渐导致膜筏破坏,从而影响与此类膜结构域相关的细胞功能。

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