Excitatory Neurons Derived from Human-Induced Pluripotent Stem Cells Show Transcriptomic Differences in Alzheimer’s Patients from Controls

Author:

Sagar Ram12ORCID,Azoidis Ioannis12ORCID,Zivko Cristina12ORCID,Xydia Ariadni12ORCID,Oh Esther S.234ORCID,Rosenberg Paul B.24,Lyketsos Constantine G.24ORCID,Mahairaki Vasiliki12,Avramopoulos Dimitrios12ORCID

Affiliation:

1. Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

2. The Richman Family Precision Medicine Center of Excellence in Alzheimer’s Disease, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA

3. Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA

4. Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA

Abstract

The recent advances in creating pluripotent stem cells from somatic cells and differentiating them into a variety of cell types is allowing us to study them without the caveats associated with disease-related changes. We generated induced Pluripotent Stem Cells (iPSCs) from eight Alzheimer’s disease (AD) patients and six controls and used lentiviral delivery to differentiate them into excitatory glutamatergic neurons. We then performed RNA sequencing on these neurons and compared the Alzheimer’s and control transcriptomes. We found that 621 genes show differences in expression levels at adjusted p < 0.05 between the case and control derived neurons. These genes show significant overlap and directional concordance with genes reported from a single-cell transcriptome study of AD patients; they include five genes implicated in AD from genome-wide association studies and they appear to be part of a larger functional network as indicated by an excess of interactions between them observed in the protein–protein interaction database STRING. Exploratory analysis with Uniform Manifold Approximation and Projection (UMAP) suggests distinct clusters of patients, based on gene expression, who may be clinically different. Our research outcomes will enable the precise identification of distinct biological subtypes among individuals with Alzheimer’s disease, facilitating the implementation of tailored precision medicine strategies.

Funder

JOHNS HOPKINS Richman Family Precision Medicine Center of Excellence in Alzheimer's DiseaseR

National Institutes of Health

Publisher

MDPI AG

Subject

General Medicine

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