Comparing Alzheimer's genes in African, European, and Amerindian induced pluripotent stem cell–derived microglia

IF 11.1 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's & Dementia Pub Date : 2025-02-26 DOI:10.1002/alz.70031
Sofia Moura, Luciana Bertholim Nasciben, Aura M. Ramirez, Lauren Coombs, Joe Rivero, Derek J. Van Booven, Brooke A. DeRosa, Kara L. Hamilton-Nelson, Patrice L. Whitehead, Larry D. Adams, Takiyah D. Starks, Pedro R. Mena, Maryenela Illanes-Manrique, Sergio Tejada, Goldie S. Byrd, Mario R. Cornejo-Olivas, Briseida E. Feliciano-Astacio, Karen Nuytemans, Liyong Wang, Margaret A. Pericak-Vance, Derek M. Dykxhoorn, Farid Rajabli, Anthony J. Griswold, Juan I. Young, Jeffery M. Vance
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Abstract

INTRODUCTION

Genome-wide association studies (GWAS) studies in Alzheimer's disease (AD) demonstrate ancestry-specific loci. Previous studies in the regulatory architecture have only been conducted in Europeans (EUs), thus studies in additional ancestries are needed. Given the prevalence of AD genes expressed in microglia, we initiated our studies in induced pluripotent stem cell (iPSC) -derived microglia.

METHODS

We created iPSC-derived microglia from 13 individuals of either high Amerindian (AI), African (AF), or EU global ancestry, including both AD and controls. RNA-seq, ATAC-seq, and pathway analyses were compared between ancestries in both AD and non-AD genes.

RESULTS

Twelve AD genes were differentially expressed genes (DEGs) and/or accessible between ancestries, including ABI3, CTSB, and MS4A6A. A total of 5% of all genes had differential ancestral expression, but differences in accessibility were less than 1%. The DEGs were enriched in known AD pathways.

DISCUSSION

This resource will be valuable in evaluating AD in admixed populations and other neurological disorders and understanding the AD risk differences between populations.

Highlights

  • First comparison of the genomics of AI, AF, and EU microglia.
  • Report differences in expression and accessibility of AD genes between ancestries.
  • Ancestral expression differences are greater than differences in accessibility.
  • Good transcriptome correlation was seen between brain and iPSC-derived microglia.
  • Differentially expressed AD genes were in known AD pathways.

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比较非洲、欧洲和美洲印第安人诱导的多能干细胞衍生的小胶质细胞的阿尔茨海默病基因
阿尔茨海默病(AD)的全基因组关联研究(GWAS)证实了遗传特异性位点。先前的监管架构研究仅在欧洲(eu)进行,因此需要对其他祖先进行研究。鉴于阿尔茨海默病基因在小胶质细胞中表达的普遍性,我们开始了对诱导多能干细胞(iPSC)衍生的小胶质细胞的研究。方法:我们从13个高美洲印第安人(AI)、非洲人(AF)或欧盟全球血统的个体(包括AD和对照)中创建了ipsc衍生的小胶质细胞。RNA-seq, ATAC-seq和通路分析比较了AD和非AD基因的祖先。结果12个AD基因存在差异表达基因(DEGs)和/或可接近,包括ABI3、CTSB和MS4A6A。所有基因中有5%的基因具有差异祖先表达,但可及性差异小于1%。deg在已知的AD通路中富集。该资源对于评估混合人群和其他神经系统疾病的AD以及了解人群之间AD风险差异具有重要价值。AI、AF和EU小胶质细胞基因组学的首次比较。报告不同祖先之间阿尔茨海默病基因的表达和可及性差异。祖先表达差异大于可及性差异。在大脑和ipsc衍生的小胶质细胞之间发现了良好的转录组相关性。差异表达的AD基因存在于已知的AD通路中。
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来源期刊
Alzheimer's & Dementia
Alzheimer's & Dementia 医学-临床神经学
CiteScore
14.50
自引率
5.00%
发文量
299
审稿时长
3 months
期刊介绍: Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.
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