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Ecto-GPR37: a potential biomarker for Parkinson's disease
Xavier Morató1,2,3, Paula Garcia-Esparcia2,4,5, Josep Argerich1,2
1Pharmacology Unit, Department of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences, Institute of Neurosciences, University of Barcelona, L'Hospitalet de Llobregat, Spain.
Translational Neurodegeneration
|February 27, 2021
Summary
GPR37 is upregulated in Parkinson's disease (PD) substantia nigra and its cleaved peptides are elevated in cerebrospinal fluid, suggesting GPR37 as a potential PD biomarker.
Area of Science:
- Neuroscience
- Biomarker Discovery
Background:
- Parkinson's disease (PD) lacks reliable biomarkers.
- α-Synuclein has shown inconclusive results as a PD biomarker.
- GPR37 is implicated in parkinsonism.
Purpose of the Study:
- Investigate GPR37 upregulation in sporadic PD.
- Assess GPR37 as a potential PD biomarker.
Main Methods:
- Analyzed GPR37 protein and mRNA in postmortem substantia nigra from PD patients.
- Detected and quantified N-terminus-cleaved GPR37 (ecto-GPR37) peptides in cerebrospinal fluid (CSF) using mass spectrometry and immunoassay.
- Compared CSF ecto-GPR37 levels in PD, neurological control, and Alzheimer's disease patients.
Main Results:
- GPR37 protein and mRNA were significantly increased in sporadic PD substantia nigra.
- CSF ecto-GPR37 peptides were elevated in PD patients.
- CSF α-synuclein levels did not differ between PD patients and controls.
- GPR37 expression and CSF ecto-GPR37 levels were unaltered in Alzheimer's disease patients.
Conclusions:
- GPR37 expression is elevated in the substantia nigra of sporadic PD patients.
- CSF ecto-GPR37 is significantly increased in PD patients but not AD patients.
- GPR37 warrants further investigation as a potential PD biomarker.
Keywords:
Alzheimer’s diseaseBiomarkerCerebrospinal fluidGPR37Orphan receptorPael-RParkinson’s diseaseα-SynucleinMore Related Videos
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