Movement disorders : official journal of the Movement Disorder Society · 2025
Evaluation of Induced Pluripotent Stem Cell-Derived Dopaminergic Neurons from Siblings with Gaucher Disease Discordant for Parkinsonism.
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Hertz Ellen, Rytel Krystyna, Perez Gani, Hao Ying, Li Ziyi, Ma Charis, Andersh Kate, Qi Yue Andy, Ryan Emory, Lopez Grisel, Tayebi Nahid, Sidransky Ellen, Chen Yu
Аннотация
BACKGROUND: In Gaucher disease (GD), glucocerebrosidase (GCase) deficiency results from biallelic pathogenic GBA1 variants. While GBA1 variants are a major risk factor for Parkinson's disease (PD), most patients with GD never develop parkinsonism.
OBJECTIVES: To understand factors impacting PD penetrance in patients with GD by comparing induced pluripotent stem cell (iPSC)-derived dopaminergic neurons (DANs) from GD siblings discordant for PD.
METHODS: iPSCs, reprogrammed from two different sibling pairs where both siblings had GD but only one developed PD, were differentiated into DANs. In one family, DAN enrichment was achieved via geneticin selection and proteomic evaluations were performed.
RESULTS: GCase and lipid substrate levels were similar in GD and GD/PD DANs. After geneticin selection, proteomic analysis of the enriched DANs showed upregulation of molecular chaperones in the GD/PD line.
CONCLUSION: PD discordance in both sets of GD siblings did not correlate with GCase or lipid substrate levels in DANs, implicating the involvement of other modifiers. Published 2025. This article is a U.S. Government work and is in the public domain in the USA. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
OBJECTIVES: To understand factors impacting PD penetrance in patients with GD by comparing induced pluripotent stem cell (iPSC)-derived dopaminergic neurons (DANs) from GD siblings discordant for PD.
METHODS: iPSCs, reprogrammed from two different sibling pairs where both siblings had GD but only one developed PD, were differentiated into DANs. In one family, DAN enrichment was achieved via geneticin selection and proteomic evaluations were performed.
RESULTS: GCase and lipid substrate levels were similar in GD and GD/PD DANs. After geneticin selection, proteomic analysis of the enriched DANs showed upregulation of molecular chaperones in the GD/PD line.
CONCLUSION: PD discordance in both sets of GD siblings did not correlate with GCase or lipid substrate levels in DANs, implicating the involvement of other modifiers. Published 2025. This article is a U.S. Government work and is in the public domain in the USA. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.