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阿尔茨海默病中的簇集素:机制、遗传学及其他病理学的启示

Clusterin in Alzheimer's Disease: Mechanisms, Genetics, and Lessons From Other Pathologies.

作者信息

Foster Evangeline M, Dangla-Valls Adrià, Lovestone Simon, Ribe Elena M, Buckley Noel J

机构信息

Department of Psychiatry, University of Oxford, Oxford, United Kingdom.

出版信息

Front Neurosci. 2019 Feb 28;13:164. doi: 10.3389/fnins.2019.00164. eCollection 2019.

Abstract

Clusterin (CLU) or APOJ is a multifunctional glycoprotein that has been implicated in several physiological and pathological states, including Alzheimer's disease (AD). With a prominent extracellular chaperone function, additional roles have been discussed for clusterin, including lipid transport and immune modulation, and it is involved in pathways common to several diseases such as cell death and survival, oxidative stress, and proteotoxic stress. Although clusterin is normally a secreted protein, it has also been found intracellularly under certain stress conditions. Multiple hypotheses have been proposed regarding the origin of intracellular clusterin, including specific biogenic processes leading to alternative transcripts and protein isoforms, but these lines of research are incomplete and contradictory. Current consensus is that intracellular clusterin is most likely to have exited the secretory pathway at some point or to have re-entered the cell after secretion. Clusterin's relationship with amyloid beta (Aβ) has been of great interest to the AD field, including clusterin's apparent role in altering Aβ aggregation and/or clearance. Additionally, clusterin has been more recently identified as a mediator of Aβ toxicity, as evidenced by the neuroprotective effect of knockdown and knockout in rodent and human iPSC-derived neurons. is also the third most significant genetic risk factor for late onset AD and several variants have been identified in . Although the exact contribution of these variants to altered AD risk is unclear, some have been linked to altered expression at both mRNA and protein levels, altered cognitive and memory function, and altered brain structure. The apparent complexity of clusterin's biogenesis, the lack of clarity over the origin of the intracellular clusterin species, and the number of pathophysiological functions attributed to clusterin have all contributed to the challenge of understanding the role of clusterin in AD pathophysiology. Here, we highlight clusterin's relevance to AD by discussing the evidence linking clusterin to AD, as well as drawing parallels on how the role of clusterin in other diseases and pathways may help us understand its biological function(s) in association with AD.

摘要

聚集素(CLU)或载脂蛋白J是一种多功能糖蛋白,与多种生理和病理状态有关,包括阿尔茨海默病(AD)。聚集素具有显著的细胞外伴侣功能,还被认为具有其他作用,包括脂质转运和免疫调节,并且参与多种疾病共有的途径,如细胞死亡与存活、氧化应激和蛋白毒性应激。虽然聚集素通常是一种分泌蛋白,但在某些应激条件下也在细胞内被发现。关于细胞内聚集素的起源提出了多种假说,包括导致替代转录本和蛋白质异构体的特定生物发生过程,但这些研究线索并不完整且相互矛盾。目前的共识是,细胞内聚集素很可能在某个时间点离开了分泌途径,或者在分泌后重新进入了细胞。聚集素与淀粉样β蛋白(Aβ)的关系一直是AD领域非常感兴趣的内容,包括聚集素在改变Aβ聚集和/或清除方面的明显作用。此外,聚集素最近被确定为Aβ毒性的介质,在啮齿动物和人诱导多能干细胞衍生的神经元中,敲低和敲除聚集素具有神经保护作用就证明了这一点。聚集素也是晚发性AD的第三大重要遗传风险因素,并且已经在其中鉴定出了几种变体。虽然这些变体对AD风险改变的确切贡献尚不清楚,但一些变体与mRNA和蛋白质水平上聚集素表达的改变、认知和记忆功能的改变以及脑结构的改变有关。聚集素生物发生的明显复杂性、细胞内聚集素种类起源的不明确性以及归因于聚集素的病理生理功能数量,都导致了理解聚集素在AD病理生理学中作用的挑战。在这里,我们通过讨论将聚集素与AD联系起来的证据,以及比较聚集素在其他疾病和途径中的作用如何可能帮助我们理解其与AD相关的生物学功能,来突出聚集素与AD的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f96/6403191/2cc104f2ab20/fnins-13-00164-g001.jpg

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