INSERM, U744, Université de Lille 2, Institut Pasteur de Lille, BP 245,1, rue du professeur Calmette, Lille cedex, France.
Mol Psychiatry. 2009 Nov;14(11):1004-16. doi: 10.1038/mp.2009.10. Epub 2009 Feb 10.
The only recognized genetic determinant of the common forms of Alzheimer's disease (AD) is the epsilon 4 allele of the apolipoprotein E gene (APOE). To identify new candidate genes, we recently performed transcriptomic analysis of 2741 genes in chromosomal regions of interest using brain tissue of AD cases and controls. From 82 differentially expressed genes, 1156 polymorphisms were genotyped in two independent discovery subsamples (n=945). Seventeen genes exhibited at least one polymorphism associated with AD risk, and following correction for multiple testing, we retained the interleukin (IL)-33 gene. We first confirmed that the IL-33 expression was decreased in the brain of AD cases compared with that of controls. Further genetic analysis led us to select three polymorphisms within this gene, which we analyzed in three independent case-control studies. These polymorphisms and a resulting protective haplotype were systematically associated with AD risk in non-APOE epsilon 4 carriers. Using a large prospective study, these associations were also detected when analyzing the prevalent and incident AD cases together or the incident AD cases alone. These polymorphisms were also associated with less cerebral amyloid angiopathy (CAA) in the brain of non-APOE epsilon 4 AD cases. Immunohistochemistry experiments finally indicated that the IL-33 expression was consistently restricted to vascular capillaries in the brain. Moreover, IL-33 overexpression in cellular models led to a specific decrease in secretion of the A beta(40) peptides, the main CAA component. In conclusion, our data suggest that genetic variants in IL-33 gene may be associated with a decrease in AD risk potentially in modulating CAA formation.
阿尔茨海默病(AD)的常见形式唯一被确认的遗传决定因素是载脂蛋白 E 基因(APOE)的 epsilon 4 等位基因。为了确定新的候选基因,我们最近使用 AD 病例和对照的脑组织,对感兴趣的染色体区域的 2741 个基因进行了转录组分析。从 82 个差异表达的基因中,在两个独立的发现子样本(n=945)中对 1156 个多态性进行了基因分型。17 个基因表现出至少一个与 AD 风险相关的多态性,并且在进行多次测试校正后,我们保留了白细胞介素(IL)-33 基因。我们首先证实与对照组相比,AD 病例的大脑中 IL-33 表达降低。进一步的遗传分析使我们选择了该基因内的三个多态性,我们在三个独立的病例对照研究中分析了这些多态性。这些多态性和一个产生保护作用的单倍型与非 APOE epsilon 4 携带者的 AD 风险系统性相关。使用一个大型前瞻性研究,当分析所有的 AD 病例或仅分析新发病例时,我们也检测到了这些关联。这些多态性也与非 APOE epsilon 4 AD 病例的脑内少的淀粉样血管病(CAA)相关。免疫组织化学实验最终表明,IL-33 表达始终局限于大脑中的血管毛细血管。此外,细胞模型中的 IL-33 过表达导致 A beta(40)肽的分泌特异性减少,这是 CAA 的主要成分。总之,我们的数据表明,IL-33 基因中的遗传变异可能与 AD 风险的降低相关,可能是通过调节 CAA 的形成。