Heidari Fatemeh, Ansstas George, Ajamian Farzam
Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.
Division of Oncology, Washington University, School of Medicine, St. Louis, Missouri, USA.
Gerontology. 2022;68(4):421-430. doi: 10.1159/000518820. Epub 2021 Sep 16.
BACKGROUND/AIMS: In despite of conflicting results among different ethnic groups, the rs3865444 of CD33 gene has previously been identified as a risk factor for late-onset Alzheimer's disease (LOAD).This study was aimed to evaluate the association between rs3865444 SNP with LOAD occurrence, and to investigate whether CD33 mRNA expression will change in the leukocytes of peripheral blood in LOAD patients.
The rs3865444 polymorphism was genotyped in 233 LOAD and 238 control subjects using the Tetra-ARMS-PCR method. CD33 mRNAs expression in leukocytes were assessed and analyzed using the real-time qPCR method. We used in silico approach to analyze potential effects imparted by rs3865444 polymorphism in LOAD pathogenesis.
Our results show a significant increase in CD33 mRNA expression levels in white blood cells of LOAD patients, however, the association between CD33 rs3865444 polymorphism and LOAD was found to be not significant. We also noticed that LOAD patients with the C/A genotype had higher CD33 mRNA levels in their peripheral blood than those of the control group.
rs3865444, located upstream of the 5'CD33 coding region, might positively influence CD33 mRNAs expression in leukocytes of LOAD versus healthy people. This is likely to happen through interfering rs3865444 (C) with the functional activity of several other transcription factors given that rs3865444 is in linkage disequilibrium with other functional polymorphisms in this coding region according to an in silico study. We propose that CD33 mRNAs elevation in peripheral immune cells - as a potential biomarker in LOAD - is related to peripheral immune system impairment.
背景/目的:尽管不同种族群体的研究结果存在冲突,但CD33基因的rs3865444先前已被确定为晚发性阿尔茨海默病(LOAD)的一个风险因素。本研究旨在评估rs3865444单核苷酸多态性(SNP)与LOAD发生之间的关联,并调查LOAD患者外周血白细胞中CD33 mRNA表达是否会发生变化。
采用四引物扩增受阻突变系统聚合酶链反应(Tetra-ARMS-PCR)方法对233例LOAD患者和238例对照者的rs3865444多态性进行基因分型。使用实时定量聚合酶链反应(qPCR)方法评估并分析白细胞中CD33 mRNA的表达。我们采用计算机模拟方法分析rs3865444多态性在LOAD发病机制中的潜在作用。
我们的结果显示LOAD患者白细胞中CD33 mRNA表达水平显著升高,然而,发现CD33 rs3865444多态性与LOAD之间的关联并不显著。我们还注意到,C/A基因型的LOAD患者外周血中CD33 mRNA水平高于对照组。
位于CD33编码区5'上游的rs3865444可能对LOAD患者与健康人白细胞中CD33 mRNA的表达产生正向影响。鉴于根据计算机模拟研究rs3865444与该编码区的其他功能多态性处于连锁不平衡状态,这可能是通过干扰rs3865444(C)与其他几种转录因子的功能活性而发生。我们提出外周免疫细胞中CD33 mRNA升高——作为LOAD的一种潜在生物标志物——与外周免疫系统损伤有关。