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Changes in iPSC-astrocyte morphology reflect Alzheimer’s disease patient clinical markers

Title: Changes in iPSC-astrocyte morphology reflect Alzheimer’s disease patient clinical markers
Authors: Rowland HA; Miller G; Liu Q; Li S; Sharp NR; Ng B; Wei T; Arunasalam K; Koychev I; Hedegaard A; Ribe EM; Chan D; Chessell T; Kocagoncu E; Lawson J; Malhotra P; Ridha BH; Rowe JB; Thomas AJ; Zamboni G; Zetterberg H; Cader MZ; Wade-Martins R; Lovestone S; Nevado-Holgado A; Kormilitzin A; Buckley NJ
Source: Stem Cells, 1 March 2025
Publisher Information: Oxford University Press
Publication Year: 2025
Collection: Newcastle University Library ePrints Service
Description: © The Author(s) 2024.Human induced pluripotent stem cells (iPSCs) provide powerful cellular models of Alzheimer’s disease (AD) and offer many advantages over nonhuman models, including the potential to reflect variation in individual-specific pathophysiology and clinical symptoms. Previous studies have demonstrated that iPSC-neurons from individuals with Alzheimer’s disease (AD) reflect clinical markers, including β-amyloid (Aβ) levels and synaptic vulnerability. However, despite neuronal loss being a key hallmark of AD pathology, many risk genes are predominantly expressed in glia, highlighting them as potential therapeutic targets. In this work iPSC-derived astrocytes were generated from a cohort of individuals with high versus low levels of the inflammatory marker YKL-40, in their cerebrospinal fluid (CSF). iPSC-derived astrocytes were treated with exogenous Aβ oligomers and high content imaging demonstrated a correlation between astrocytes that underwent the greatest morphology change from patients with low levels of CSF-YKL-40 and more protective APOE genotypes. This finding was subsequently verified using similarity learning as an unbiased approach. This study shows that iPSC-derived astrocytes from AD patients reflect key aspects of the pathophysiological phenotype of those same patients, thereby offering a novel means of modelling AD, stratifying AD patients and conducting therapeutic screens.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/305124; https://eprints.ncl.ac.uk/fulltext.aspx?url=305124/D96E8C7B-7D07-4082-8286-EA2FA881AE1D.pdf&pub_id=305124
Availability: https://eprints.ncl.ac.uk/305124
Rights: https://creativecommons.org/licenses/by-nc/4.0/
Accession Number: edsbas.9161015E
Database: BASE