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G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination
Open accessAbstract
GPR56, an orphan G protein-coupled receptor (GPCR) from the family of adhesion GPCRs, plays an indispensable role in cortical development and lamination. Mutations in the GPR56 gene cause a malformed cerebral cortex in both humans and mice that resembles cobblestone lissencephaly, which is characterized by overmigration of neurons beyond the pial basement membrane. However, the molecular mechanisms through which GPR56 regulates cortical development remain elusive due to the unknown status of its ligand. Here we identify collagen, type III, alpha-1 (gene symbol Col3a1 ) as the ligand of GPR56 through an in vitro biotinylation/proteomics approach. Further studies demonstrated that Col3a1 null mutant mice exhibit overmigration of neurons beyond the pial basement membrane and a cobblestone-like cortical malformation similar to the phenotype seen in Gpr56 null mutant mice. Functional studies suggest that the interaction of collagen III with its receptor GPR56 inhibits neural migration in vitro. As for intracellular signaling, GPR56 couples to the Gα 12/13 family of G proteins and activates RhoA pathway upon ligand binding. Thus, collagen III regulates the proper lamination of the cerebral cortex by acting as the major ligand of GPR56 in the developing brain.
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“GPR56 encodes an adhesion heterotrimeric guanine nucleotide–binding protein (G protein)–coupled receptor that is highly expressed in cortical progenitors (7, 16) and binds extracellular matrix proteins (17).”
From Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning (2014) · cites this paper as [17]
In the citing paper
“GPR56 likely influences progenitor proliferation by stabilizing the basal process of radial neuroepithelial progenitors”
From Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning (2014) · cites this paper as [17]
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Metadata
- Authors
- Luo, R., Jeong, S.-J., Jin, Z., Strokes, N., Li, S., & Piao, X.
- Affiliations
- Boston Children's Hospital (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2011-07-18
- Volume
- 108
- Issue
- 31
- Pages
- 12925-12930
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3150909
- OpenAlex
- W2083047610
- Cited by
- 290
- References
- 50
- Citations by year
- 2026: 14 · 2025: 21 · 2024: 15 · 2023: 20 · 2022: 17 · 2021: 23 · 2020: 22 · 2019: 26 · 2018: 15 · 2017: 14 · 2016: 26 · 2015: 22 · 2014: 19 · 2013: 18 · 2012: 16
- FWCI
- 5.66
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS057536)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- GPR56, type III collagen, COL3A1, G protein-coupled receptor ligands, cortical lamination, cortical development, neuronal migration, cobblestone lissencephaly, adhesion GPCRs, RhoA signaling, cerebral cortex malformation
- MeSH terms
- Animals, Basement Membrane, Brain, Cell Movement, Cells, Cultured, Cerebral Cortex, Humans, Immunohistochemistry, Neurons, Protein Binding, Recombinant Proteins, Immunoblotting, Microscopy, Immunoelectron, Mice, Knockout, rhoA GTP-Binding Protein, Collagen Type III, NIH 3T3 Cells, Receptors, G-Protein-Coupled, GTP-Binding Protein alpha Subunits, G12-G13, Immunoprecipitation, Mice, Cobblestone Lissencephaly
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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