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GPR162 is a beta cell CART receptor.
Lindqvist, Andreas; Abels, Mia; Shcherbina, Liliya; Ngara, Mtakai; Kryvokhyzha, Dmytro; Chriett, Sabrina; Riva, Matteo; Fajul, Abul; Barghouth, Mohammad; Luan, Cheng; Eliasson, Lena; Larsen, Olav; Rosenkilde, Mette M; Zhang, Enming; Renström, Erik; Wierup, Nils.
Affiliation
  • Lindqvist A; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Abels M; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Shcherbina L; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Ngara M; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Kryvokhyzha D; Diabetic Complications, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Chriett S; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Riva M; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Fajul A; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
  • Barghouth M; Islet Pathophysiology, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Luan C; Islet Pathophysiology, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Eliasson L; Islet Cell Exocytosis, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Larsen O; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Rosenkilde MM; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Zhang E; Islet Pathophysiology, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Renström E; Islet Pathophysiology, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, CRC, Malmö, Sweden.
  • Wierup N; Neuroendocrine Cell Biology, Lund University Diabetes Centre, Department for Experimental Medical Science, Lund University, CRC, Malmö, Sweden.
iScience ; 26(12): 108416, 2023 Dec 15.
Article in En | MEDLINE | ID: mdl-38077141
ABSTRACT
Cocaine and amphetamine-regulated transcript (CART) is expressed in pancreatic islet cells and neuronal elements. We have previously established insulinotropic actions of CART in human and rodent islets. The receptor for CART in the pancreatic beta cells is unidentified. We used RNA sequencing of Cartpt knockdown (KD) INS-1 832/13 cells and identified GPR162 as the most Cartpt-regulated receptor. We therefore tested if GPR162 mediates the effects of CART in beta cells. Binding of CART to GPR162 was established using proximity ligation assay, radioactive binding, and co-immunoprecipitation, and KD of Gpr162 mRNA caused reduced binding. Gpr162 KD cells had blunted CARTp-induced exocytosis, and reduced CARTp-induced insulin secretion. Furthermore, we identified a hitherto undescribed GPR162-dependent role of CART as a regulator of cytoskeletal arrangement. Thus, our findings provide mechanistic insight into the effect of CART on insulin secretion and show that GPR162 is the CART receptor in beta cells.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article Affiliation country: Suecia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article Affiliation country: Suecia