Genetic variants in
GBA1
, encoding the lysosomal enzyme glucocerebrosidase (GCase), represent the strongest genetic risk factor for Parkinson’s disease (PD) and provide a mechanistic link between Gaucher disease (GD) and PD. While biallelic
GBA1
mutations cause GD, heterozygous variants confer an increased, age-dependent risk of PD, with mutation-specific differences in penetrance, age at onset, cognitive decline, and survival. This review critically examines the molecular and clinical spectrum of
GBA1
-associated PD (GBA1-PD), highlighting the relationship between variant severity, lysosomal dysfunction, and disease progression. We discuss two major, partially overlapping pathogenic frameworks underlying
GBA1
-PD: loss-of-function mechanisms associated with reduced GCase activity, glycosphingolipid accumulation, and impaired autophagy–lysosomal pathways, and toxic gain-of-function mechanisms driven by mutant GCase misfolding, endoplasmic reticulum stress, and proteostatic imbalance. Increasing evidence suggests that these mechanisms converge on α-synuclein aggregation and dopaminergic neurodegeneration. We further summarize emerging disease-modifying therapeutic strategies, including small-molecule GCase activators, pharmacological chaperones, substrate reduction therapies, acid ceramidase inhibitors, and gene therapies. Although clinical outcomes have been heterogeneous,
GBA1
-associated PD represents a valuable model for precision medicine, illustrating how genetic stratification can guide mechanism-based therapeutic development in neurodegeneration.
Christiane Oleksy, I. Boussaad, Z. Landoulsi et al.· npj Parkinson's Disease· 0 citations
Astrocytes are increasingly recognised as essential contributors to both physiological brain function and neurodegenerative diseases. Here, we describe how the Parkinson’s disease (PD)-associated mutation LRRK2-G2019S affects astrocytes using autoptic brain samples and PD patient-specific 3D midbrain organoids and 2D astrocytes derived from induced pluripotent stem cells. In autoptic midbrain samples from LRRK2-G2019S patients, we observed a reduction in GFAP⁺ astrocytes but increased branching, together with transcriptional signatures consistent with altered astrocyte function. We also observed delayed astrocyte differentiation in PD patient-specific midbrain organoids, accompanied by altered astrocyte transcriptomic profiles revealed by single-cell RNA sequencing. This defective differentiation contributes to the acquisition of a senescent-like phenotype. In 2D cultures, astrocyte differentiation from LRRK2-G2019S precursor cells was associated with early apoptosis and altered Wnt/β-catenin and TGFβ signalling compared to LRRK2-WT cultures. Notably, pharmacological activation of the developmental transcription factor NR2F1, downregulated in LRRK2-G2019S models, reduced astrocyte cell death and senescence-like phenotypes. Together, these data show that LRRK2-G2019S impairs astrocyte specification and predisposes to a senescent phenotype.
Lisa M. Smits, S. Magni, K. Grzyb et al.· npj Parkinson's Disease· 0 citations