GPR162 is a beta cell CART receptor
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Standard
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.
I: iScience, Bind 26, Nr. 12, 108416, 2023.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - GPR162 is a beta cell CART receptor
AU - Lindqvist, Andreas
AU - Abels, Mia
AU - Shcherbina, Liliya
AU - Ngara, Mtakai
AU - Kryvokhyzha, Dmytro
AU - Chriett, Sabrina
AU - Riva, Matteo
AU - Fajul, Abul
AU - Barghouth, Mohammad
AU - Luan, Cheng
AU - Eliasson, Lena
AU - Larsen, Olav
AU - Rosenkilde, Mette M.
AU - Zhang, Enming
AU - Renström, Erik
AU - Wierup, Nils
N1 - Publisher Copyright: © 2023 The Author(s)
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
KW - Biological sciences
KW - Endocrinology
KW - Natural sciences
KW - Physiology
UR - http://www.scopus.com/inward/record.url?scp=85177871704&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2023.108416
DO - 10.1016/j.isci.2023.108416
M3 - Journal article
C2 - 38077141
AN - SCOPUS:85177871704
VL - 26
JO - iScience
JF - iScience
SN - 2589-0042
IS - 12
M1 - 108416
ER -
ID: 375312571