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内溶酶体在原代培养神经元中的 LDL 胆固醇诱导的阿尔茨海默病样病变中的作用。

Endolysosome involvement in LDL cholesterol-induced Alzheimer's disease-like pathology in primary cultured neurons.

机构信息

Department of Pharmacology, Physiology and Therapeutics, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA.

出版信息

Life Sci. 2012 Dec 10;91(23-24):1159-68. doi: 10.1016/j.lfs.2012.04.039. Epub 2012 May 11.

Abstract

AIMS

Elevated levels of circulating cholesterol are extrinsic factors contributing to the pathogenesis of sporadic Alzheimer's disease (AD). We showed previously that rabbits fed a cholesterol-enriched diet exhibited blood-brain barrier (BBB) dysfunction, increased accumulation of apolipoprotein B (ApoB) in brain neurons, and endolysosomes in brain had disturbed structures and functions. These effects were linked to increased amyloid beta (Aβ) production, increased tau-pathology, and disrupted synaptic integrity. Because pathological changes to endolysosomes represent a very early event in sporadic AD, we determined here the extent to which ApoB-containing LDL cholesterol altered the structure and function of endolysosomes and contributed to the development of AD-like pathology in primary cultured neurons.

MAIN METHODS

Cholesterol distribution and endolysosome morphology were determined histologically. Endolysosome pH was measured ratio-metrically with LysoSensor dye. Endolysosome enzyme activity was measured for acid phosphatase, cathepsins B and D, and beta-site APP cleaving enzyme 1 (BACE-1). AD-like pathologies, including increased production of Aβ, increased tau-pathology, and disrupted synaptic integrity were determined using ELISA, immunoblotting, and immunostaining techniques.

KEY FINDINGS

Treatment of neurons with ApoB-containing LDL cholesterol increased endolysosome accumulation of cholesterol, enlarged endolysosomes, and elevated endolysosome pH. In addition, ApoB-containing LDL cholesterol increased endolysosome accumulation of BACE-1, enhanced BACE-1 activity, increased Aβ levels, increased levels of phosphorylated tau, and decreased levels of synaptophysin.

SIGNIFICANCE

Our findings suggest strongly that alterations in the structure and function of endolysosomes play a key role in the exhibition of pathological features of AD that result from neuronal exposure to ApoB-containing LDL cholesterol.

摘要

目的

循环胆固醇水平升高是导致散发性阿尔茨海默病(AD)发病的外在因素。我们之前的研究表明,喂食富含胆固醇的饮食的兔子表现出血脑屏障(BBB)功能障碍、载脂蛋白 B(ApoB)在脑神经元中的积累增加以及脑内内溶酶体结构和功能紊乱。这些影响与淀粉样β(Aβ)生成增加、tau 病理学增加和突触完整性破坏有关。由于内溶酶体的病理变化代表散发性 AD 的一个非常早期的事件,因此我们在这里确定载脂蛋白 B 含量的 LDL 胆固醇改变内溶酶体的结构和功能的程度,并有助于原代培养神经元中 AD 样病理学的发展。

主要方法

通过组织学方法确定胆固醇的分布和内溶酶体的形态。用 LysoSensor 染料比色法测量内溶酶体 pH 值。用酸性磷酸酶、组织蛋白酶 B 和 D 以及β位 APP 切割酶 1(BACE-1)对内溶酶体酶活性进行测量。采用 ELISA、免疫印迹和免疫染色技术测定 AD 样病变,包括 Aβ生成增加、tau 病理学增加和突触完整性破坏。

主要发现

用载脂蛋白 B 含量的 LDL 胆固醇处理神经元会增加内溶酶体胆固醇的积累,使内溶酶体增大,并升高内溶酶体 pH 值。此外,载脂蛋白 B 含量的 LDL 胆固醇增加了内溶酶体中 BACE-1 的积累,增强了 BACE-1 的活性,增加了 Aβ水平,增加了磷酸化 tau 的水平,降低了突触小泡蛋白的水平。

意义

我们的研究结果强烈表明,内溶酶体结构和功能的改变在神经元暴露于载脂蛋白 B 含量的 LDL 胆固醇导致的 AD 病理特征的表现中起着关键作用。

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