Trafficking regulation of proteins in Alzheimer's disease.

Trafficking regulation of proteins in Alzheimer's disease.
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DOI:
10.1186/1750-1326-9-6
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发表时间:
2014-01-11
影响因子:
15.1
通讯作者:
Zhang YW
Zhang YW
中科院分区:
医学1区
文献类型:
--
作者:
Jiang S;Li Y;Zhang X;Bu G;Xu H;Zhang YW

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β-淀粉样蛋白(A-β)多肽被认为是阿尔茨海默病(AD)发病机制中的关键决定因素。β是通过β-淀粉样前体蛋白(APP)被β-和γ-分泌酶顺序切割而产生的。APP及其相关的分泌物是一种跨膜蛋白,以高度调控的方式通过分泌途径进行运输。它们在细胞内转运的扰动可能会影响这些蛋白之间的动态相互作用,从而改变Aβ的生成,加速疾病的发病。在这里,我们综述了最近的进展,阐明了调控这些必要的蛋白质组分在AD的细胞内运输。
The β-amyloid (Aβ) peptide has been postulated to be a key determinant in the pathogenesis of Alzheimer’s disease (AD). Aβ is produced through sequential cleavage of the β-amyloid precursor protein (APP) by β- and γ-secretases. APP and relevant secretases are transmembrane proteins and traffic through the secretory pathway in a highly regulated fashion. Perturbation of their intracellular trafficking may affect dynamic interactions among these proteins, thus altering Aβ generation and accelerating disease pathogenesis. Herein, we review recent progress elucidating the regulation of intracellular trafficking of these essential protein components in AD.
LDLR相关的蛋白10(LRP10)调节淀粉样蛋白前体蛋白(APP)运输和加工:在阿尔茨海默氏病中作用的证据。
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影响因子: 15.1
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