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GPR142 Agonists Stimulate Glucose-Dependent Insulin Secretion via Gq-Dependent Signaling.
- Source :
-
PloS one [PLoS One] 2016 Apr 22; Vol. 11 (4), pp. e0154452. Date of Electronic Publication: 2016 Apr 22 (Print Publication: 2016). - Publication Year :
- 2016
-
Abstract
- GPR142 is an islet-enriched G protein-coupled receptor that has been investigated as a novel therapeutic target for the treatment of type 2 diabetes by virtue of its insulin secretagogue activity. However, the signaling pathways downstream of GPR142 and whether its stimulation of insulin release is glucose-dependent remain poorly characterized. In this study, we show that both native and synthetic GPR142 agonists can activate Gq as well as Gi signaling when GPR142 is recombinantly expressed in HEK293 cells. However, in primary pancreatic islets, a native cellular system, the insulin secretagogue activity of GPR142 agonists only requires Gq activation. In addition, our results show that stimulation of insulin secretion by GPR142 in pancreatic islets is strictly glucose-dependent.
- Subjects :
- Animals
Colforsin pharmacology
Cyclic AMP metabolism
Gene Expression Regulation
Glucose metabolism
HEK293 Cells
Humans
Insulin metabolism
Insulin Secretion
Islets of Langerhans cytology
Islets of Langerhans drug effects
Islets of Langerhans metabolism
Male
Mice
Mice, Inbred C57BL
Mitogen-Activated Protein Kinase 1 genetics
Mitogen-Activated Protein Kinase 1 metabolism
Mitogen-Activated Protein Kinase 3 genetics
Mitogen-Activated Protein Kinase 3 metabolism
Phosphorylation
Primary Cell Culture
Protein Subunits genetics
Protein Subunits metabolism
Receptors, G-Protein-Coupled genetics
Receptors, G-Protein-Coupled metabolism
Recombinant Proteins genetics
Recombinant Proteins metabolism
Signal Transduction drug effects
Signal Transduction genetics
Aminopyridines pharmacology
Glucose pharmacology
Insulin agonists
Protein Subunits agonists
Pyrazoles pharmacology
Receptors, G-Protein-Coupled agonists
Tryptophan pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 11
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 27104960
- Full Text :
- https://doi.org/10.1371/journal.pone.0154452