PUBLICATION
Multi-omics analyses of early-onset familial Alzheimer's disease and Sanfilippo syndrome zebrafish models reveal commonalities in disease mechanisms
- Authors
- Barthelson, K., Protzman, R.A., Snel, M.F., Hemsley, K., Lardelli, M.
- ID
- ZDB-PUB-250113-6
- Date
- 2025
- Source
- Biochimica et biophysica acta. Molecular basis of disease : 167651167651 (Journal)
- Registered Authors
- Lardelli, Michael
- Keywords
- Alzheimer's disease, Childhood dementia, Extracellular matrix, Lysosome, Oxidative phosphorylation, RNA-seq, Ribosome, Sanfilippo syndrome, Zebrafish
- MeSH Terms
-
- Presenilin-1/genetics
- Presenilin-1/metabolism
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- Humans
- Zebrafish*/genetics
- Alzheimer Disease*/genetics
- Alzheimer Disease*/metabolism
- Alzheimer Disease*/pathology
- Transcriptome
- Disease Models, Animal*
- Brain/metabolism
- Brain/pathology
- Proteomics/methods
- Proteome/metabolism
- Animals
- Multiomics
- Mucopolysaccharidosis III*/genetics
- Mucopolysaccharidosis III*/metabolism
- Mucopolysaccharidosis III*/pathology
- PubMed
- 39798820 Full text @ BBA Molecular Basis of Disease
Citation
Barthelson, K., Protzman, R.A., Snel, M.F., Hemsley, K., Lardelli, M. (2025) Multi-omics analyses of early-onset familial Alzheimer's disease and Sanfilippo syndrome zebrafish models reveal commonalities in disease mechanisms. Biochimica et biophysica acta. Molecular basis of disease. :167651167651.
Abstract
Sanfilippo syndrome (mucopolysaccharidosis type III, MPSIII) causes childhood dementia, while Alzheimer's disease is the most common type of adult-onset dementia. There is no cure for either of these diseases, and therapeutic options are extremely limited. Increasing evidence suggests commonalities in the pathogenesis of these diseases. However, a direct molecular-level comparison of these diseases has never been performed. Here, we exploited the power of zebrafish reproduction (large families of siblings from single mating events raised together in consistent environments) to conduct sensitive, internally controlled, comparative transcriptome and proteome analyses of zebrafish models of early-onset familial Alzheimer's disease (EOfAD, psen1Q96_K97del/+) and MPSIIIB (nagluA603fs/A603fs) within single families. We examined larval zebrafish (7 days post fertilisation), representing early disease stages. We also examined the brains of 6-month-old zebrafish, which are approximately equivalent to young adults in humans. We identified substantially more differentially expressed genes and pathways in MPS III zebrafish than in EOfAD-like zebrafish. This is consistent with MPS III being a rapidly progressing and earlier onset form of dementia. Similar changes in expression were detected between the two disease models in gene sets representing extracellular matrix receptor interactions in larvae, and the ribosome and lysosome pathways in 6-month-old adult brains. Cell type-specific changes were detected in MPSIIIB brains at 6 months of age, likely reflecting significant disturbances of oligodendrocyte, neural stem cell, and inflammatory cell functions and/or numbers. Our 'omics analyses have illuminated similar disease pathways between EOfAD and MPS III indicating where efforts to find mutually effective therapeutic strategies can be targeted.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping