PSEN1 mutant marmoset fibroblasts mimic multi-omic signatures of Alzheimer's disease
S Vinod KumariD, Annat HaberiD, Catrina A. SpruceiD, Duc Duong, Nicholas T. SeyfriediD, Lauren BaileyiD, Sang-Ho Choi, Stephanie Hachem, Yongshan Mou, Seung-Kwon HaiD, Jung Eun Park, Gregg E. HomanicsiD, Stacey J. Sukoff RizzoiD, Afonso C. SilvaiD, Gregory W. CarteriD
Abstract
INTRODUCTIONThe slow, age-related development of Alzheimers disease (AD) and inaccessibility of early-stage brain tissue necessitates model studies to understand its origins and progression. Non-human primate models can provide a platform for linking molecular changes to translatable phenotypes. Here, we assess fibroblast lines derived from marmosets with engineered variants in the PSEN1 gene. METHODSFibroblast cultures were obtained from 10 animals and assayed using a NanoString AD gene expression panel and label-free proteomics. We compared mutant expression changes to human AD signatures in human iPSC-derived neurons and postmortem brains to assess disease relevance. RESULTSGene products involved in amyloid-beta interaction and regulation were differentially expressed, providing evidence for the functional relevance of the engineered fibroblasts. Both gene and protein expression changes in the undifferentiated fibroblasts correlated with human iPSCs from AD donors reprogrammed into neuronal lineages, as well as postmortem brains derived from case-control cohorts. Altered expression profiles were noted based on marmoset donor sex and mutation status, highlighting underlying sex-specific biology relevant to Alzheimers disease. DISCUSSIONThese findings demonstrate that disease-relevant pathways and processes are altered in fibroblasts from mutant marmosets, emphasize the complementarity of transcriptomic and proteomic profiling in AD, and provide a roadmap for more advanced molecular studies of AD in aging marmosets and marmoset-derived cell models.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A non-human primate model of familial Alzheimer's disease
Kenya Sato, Hiroki Sasaguri, … Erika Sasaki·bioRxiv·Aug 24, 2020
- 3D bioengineered neural tissue generated from patient-derived iPSCs develops time-dependent phenotypes and transcriptional features of Alzheimer's disease
Selene Lomoio, Ravi S. Pandey, … Giuseppina Tesco·Molecular PsychiatryPeer-reviewed·Jun 26, 2023
- Identification and drug-induced reversion of molecular signatures of Alzheimers disease onset and progression in AppNL-G-F, AppNL-F and 3xTg-AD mouse models
Eduardo Pauls, Sergi Bayod, … Patrick Aloy·Genome MedicinePeer-reviewed·Oct 26, 2021
- Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction, progression, and prion-like spread of Alzheimer s disease pathogenesis
Yuriy Pomeshchik, Erika Velásquez, … Laurent Roybon·Acta Neuropathologica CommunicationsPeer-reviewed·Sep 15, 2023
- A disease similarity approach identifies short-lived Niemann-Pick type C disease mice with accelerated brain aging as a novel mouse model for Alzheimer's disease and aging research
Vikas Anil Gujjala, Isaiah Klimek, … Alaattin Kaya·bioRxiv·Apr 19, 2024
- Alzheimer's Disease-Associated Proteomic Changes in Olfactory Stem Cells Show Pathway-Level Transcriptomic Overlap
Laura M. Rantanen, Harley Robinson, … Anthony Robert White·bioRxiv·Oct 24, 2026