Cytosolic GPR37, but not GPR37L1, multimerization and its reversal by Parkin: A live cell imaging study

• Published in: The FASEB journal Vol. 35; no. 12; pp. e22055 - n/a
• Main Authors: Li, Tianyi, Oasa, Sho, Ciruela, Francisco, Terenius, Lars, Vukojević, Vladana, Svenningsson, Per
• Format: Journal Article
• Language: English
• Published: United States 01-12-2021
• Subjects: aggregation; Animals; Cell Membrane - metabolism; Cytosol - metabolism; dimerization; G protein‐coupled receptors; Medicin och hälsovetenskap; Mice; Microscopy, Confocal; Molecular Imaging; Neuroblastoma - metabolism; Neuroblastoma - pathology; Pael‐R; Parkinson disease; Parkinson Disease - metabolism; Parkinson Disease - pathology; Protein Multimerization; Receptors, G-Protein-Coupled - chemistry; Receptors, G-Protein-Coupled - metabolism; Tumor Cells, Cultured; Ubiquitin-Protein Ligases - metabolism; Parkinson disease; dimerization; aggregation; G protein-coupled receptors; Pael-R
• ISSN: 0892-6638; 1530-6860; 1530-6860
• DOI: 10.1096/fj.202101213R

Biochemical data have shown aggregated G protein‐coupled receptor 37 (GPR37) in the cytoplasm and Lewy bodies in Parkinson's disease (PD). Properly folded GPR37 at the plasma membrane appears to be neuroprotective. GPR37, and its homologue GPR37L1, are orphan G protein‐coupled receptors and their homo‐ and hetero‐dimers have not been established. We therefore examined GPR37 and GPR37L1 dimerization and extended studies of multimerization of GPR37 to live cells. In this study, we investigated GPR37 and GPR37L1 dimerization and multimerization in live cells using three quantitative imaging methods: Fluorescence Cross‐Correlation Spectroscopy, Förster Resonance Energy Transfer, and Fluorescence Lifetime Imaging Microscopy. Our data show that GPR37 and GPR37L1 form homo‐ and heterodimers in live N2a cells. Importantly, aggregation of GPR37, but not GPR37L1, was identified in the cytoplasm, which could be counteracted by Parkin overexpression. These data provide further evidence that GPR37 participate in cytosolic aggregation processes implicated in PD pathology.