Saavedra Lucila, Mohamed Amany, Ma Victoria, Kar Satyabrata, de Chaves Elena Posse
Department of Pharmacology, University of Alberta, Edmonton, Canada.
J Biol Chem. 2007 Dec 7;282(49):35722-32. doi: 10.1074/jbc.M701823200. Epub 2007 Oct 2.
Extracellular accumulation of beta-amyloid peptide (Abeta) has been linked to the development of Alzheimer disease. The importance of intraneuronal Abeta has been recognized more recently. Although considerable evidence indicates that extracellular Abeta contributes to the intracellular pool of Abeta, the mechanisms involved in Abeta uptake by neurons are poorly understood. We examined the molecular mechanisms involved in Abeta-(1-42) internalization by primary neurons in the absence of apolipoprotein E. We demonstrated that Abeta-(1-42) is more efficiently internalized by axons than by cell bodies of sympathetic neurons, suggesting that Abeta-(1-42) uptake might be mediated by proteins enriched in the axons. Although the acetylcholine receptor alpha7nAChR, previously suggested to be involved in Abeta internalization, is enriched in axons, our results indicate that it does not mediate Abeta-(1-42) internalization. Moreover, receptors of the low density lipoprotein receptor family are not essential for Abeta-(1-42) uptake in the absence of apolipoprotein E because receptor-associated protein had no effect on Abeta uptake. By expressing the inactive dynamin mutant dynK44A and the clathrin hub we found that Abeta-(1-42) internalization is independent of clathrin but dependent on dynamin, which suggests an endocytic pathway involving caveolae/lipid rafts. Confocal microscopy studies showing that Abeta did not co-localize with the early endosome marker EEA1 further support a clathrin-independent mechanism. The lack of co-localization of Abeta with caveolin in intracellular vesicles and the normal uptake of Abeta by neurons that do not express caveolin indicate that Abeta does not require caveolin either. Instead partial co-localization of Abeta-(1-42) with cholera toxin subunit B and sensitivity to reduction of cellular cholesterol and sphingolipid levels suggest a caveolae-independent, raft-mediated mechanism. Understanding the molecular events involved in neuronal Abeta internalization might identify potential therapeutic targets for Alzheimer disease.
β-淀粉样肽(Aβ)的细胞外积聚与阿尔茨海默病的发展有关。神经元内Aβ的重要性最近才得到认可。尽管大量证据表明细胞外Aβ有助于细胞内Aβ池的形成,但神经元摄取Aβ的机制仍知之甚少。我们研究了在没有载脂蛋白E的情况下,原代神经元摄取Aβ-(1-42)所涉及的分子机制。我们证明,Aβ-(1-42)被轴突摄取的效率高于交感神经元的细胞体,这表明Aβ-(1-42)的摄取可能由轴突中富集的蛋白质介导。尽管先前认为参与Aβ内化的乙酰胆碱受体α7nAChR在轴突中富集,但我们的结果表明它不介导Aβ-(1-42)的内化。此外,在没有载脂蛋白E的情况下,低密度脂蛋白受体家族的受体对于Aβ-(1-42)的摄取不是必需的,因为受体相关蛋白对Aβ摄取没有影响。通过表达无活性的发动蛋白突变体dynK44A和网格蛋白枢纽,我们发现Aβ-(1-42)的内化不依赖于网格蛋白,但依赖于发动蛋白,这表明存在一种涉及小窝/脂筏的内吞途径。共聚焦显微镜研究表明,Aβ与早期内体标记物EEA1不共定位,这进一步支持了一种不依赖网格蛋白的机制。Aβ与细胞内囊泡中的小窝蛋白不共定位,以及不表达小窝蛋白的神经元对Aβ的正常摄取表明,Aβ也不需要小窝蛋白。相反,Aβ-(1-42)与霍乱毒素亚基B的部分共定位以及对细胞胆固醇和鞘脂水平降低的敏感性表明存在一种不依赖小窝、由脂筏介导的机制。了解神经元摄取Aβ所涉及的分子事件可能会确定阿尔茨海默病的潜在治疗靶点。