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嗅受体 OR2K2 在人脉络丛中的表达作为早期散发性阿尔茨海默病的潜在标志物。

Olfactory Receptor OR2K2 Expression in Human Choroid Plexus as a Potential Marker in Early Sporadic Alzheimer's Disease.

机构信息

Neurodegenerative Diseases Group, Hospital Universitario 12 de Octubre Research Institute (imas12), 28041 Madrid, Spain.

Network Center for Biomedical Research, Neurodegenerative Diseases (CIBERNED), 28029 Madrid, Spain.

出版信息

Genes (Basel). 2024 Mar 21;15(3):385. doi: 10.3390/genes15030385.

Abstract

Epithelial cells comprising the choroid plexus (CP) form a crucial barrier between the blood and the cerebrospinal fluid, thereby assuming a central position in brain homeostasis and signaling. Mounting evidence suggests that the impairment of CP function may be a significant contributor to Alzheimer's disease (AD) pathogenesis. CP function relies on the expression of specific receptors, and the potential involvement of olfactory receptors (ORs) and taste receptors (TASRs) in chemical surveillance within the CP is being investigated. Previous studies have implicated ORs and TASRs in neurodegenerative disorders like AD, although the direct evidence of their expression in the human CP remains to be established. In this study, we conducted a transcriptomic analysis encompassing eleven and in the CP, comparing samples from healthy age-matched controls to those from patients with AD spanning Braak stages I to VI. Among these receptors, a striking finding emerged- exhibited robust expression, with a statistically significant upregulation noted at Braak stage I. Surprisingly, at the protein level, OR2K2 showed a significant decrease in both Braak stage I and VI. Additionally, we identified CP epithelial cells as the source of OR2K2 expression, where it colocalized with autophagy markers LC3 and p62. We postulate that OR2K2 could be subjected to degradation by autophagy in the early stages of AD, triggering a compensatory mechanism that leads to increased mRNA transcription. This study uncovers a potential role for OR2K2 in AD pathogenesis, offering a novel perspective on the intricate dynamics at play in this neurodegenerative disorder.

摘要

脉络丛上皮细胞构成了血脑屏障的重要组成部分,位于大脑内环境和信号传递的中心位置。越来越多的证据表明,脉络丛功能的损伤可能是阿尔茨海默病(AD)发病机制的重要因素。脉络丛功能依赖于特定受体的表达,而嗅觉受体(ORs)和味觉受体(TASRs)在脉络丛内的化学监测中的潜在作用正在研究中。先前的研究表明,ORs 和 TASRs 参与了 AD 等神经退行性疾病,尽管它们在人脉络丛中的直接表达证据仍有待建立。在这项研究中,我们进行了一项转录组分析,涵盖了 11 个 OR 和 2 个 TASR 在脉络丛中的表达,将来自健康年龄匹配对照者和 AD 患者(跨越 Braak 分期 I 至 VI)的样本进行比较。在这些受体中,一个引人注目的发现是 OR2K2 表现出强烈的表达,在 Braak 分期 I 时观察到明显的上调。令人惊讶的是,在蛋白质水平上,OR2K2 在 Braak 分期 I 和 VI 中均显著减少。此外,我们确定了脉络丛上皮细胞是 OR2K2 表达的来源,在那里它与自噬标志物 LC3 和 p62 共定位。我们推测,OR2K2 可能在 AD 的早期阶段通过自噬被降解,触发一种代偿机制,导致 mRNA 转录增加。这项研究揭示了 OR2K2 在 AD 发病机制中的潜在作用,为这一神经退行性疾病中复杂的动态提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f47f/10970182/6ec848d4f7b8/genes-15-00385-g001.jpg

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