Mouse Mutants of <i>Gpr37</i> and <i>Gpr37l1</i> Receptor Genes: Disease Modeling Applications

The vertebrate G protein–coupled receptor 37 and G protein–coupled receptor 37-like 1 (GPR37 and GPR37L1) proteins have amino acid sequence homology to endothelin and bombesin-specific receptors. The prosaposin glycoprotein, its derived peptides, and analogues have been reported to interact with and...

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Bibliographic Details
Main Authors: Marzia Massimi, Chiara Di Pietro, Gina La Sala, Rafaele Matteoni
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/8/4288
Description
Summary:The vertebrate G protein–coupled receptor 37 and G protein–coupled receptor 37-like 1 (GPR37 and GPR37L1) proteins have amino acid sequence homology to endothelin and bombesin-specific receptors. The prosaposin glycoprotein, its derived peptides, and analogues have been reported to interact with and activate both putative receptors. The <i>GPR37</i> and <i>GPR37L1</i> genes are highly expressed in human and rodent brains. <i>GPR37</i> transcripts are most abundant in oligodendrocytes and in the neurons of the <i>substantia nigra</i> and hippocampus, while the <i>GPR37L1</i> gene is markedly expressed in cerebellar Bergmann glia astrocytes. The human GPR37 protein is a substrate of parkin, and its insoluble form accumulates in brain samples from patients of inherited juvenile Parkinson’s disease. Several <i>Gpr37</i> and <i>Gpr37l1</i> mouse mutant strains have been produced and applied to extensive in vivo and ex vivo analyses of respective receptor functions and involvement in brain and other organ pathologies. The genotypic and phenotypic characteristics of the different mouse strains so far published are reported and discussed, and their current and proposed applications to human disease modeling are highlighted.
ISSN:1661-6596
1422-0067