TY - JOUR
T1 - Checkpoint kinase 2 controls insulin secretion and glucose homeostasis
AU - Chong, Angie Chi Nok
AU - Vandana, J. Jeya
AU - Jeng, Ginnie
AU - Li, Ge
AU - Meng, Zihe
AU - Duan, Xiaohua
AU - Zhang, Tuo
AU - Qiu, Yunping
AU - Duran-Struuck, Raimon
AU - Coker, Kimberly
AU - Wang, Wei
AU - Li, Yanjing
AU - Min, Zaw
AU - Zuo, Xi
AU - de Silva, Neranjan
AU - Chen, Zhengming
AU - Naji, Ali
AU - Hao, Mingming
AU - Liu, Chengyang
AU - Chen, Shuibing
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2024/5
Y1 - 2024/5
N2 - After the discovery of insulin, a century ago, extensive work has been done to unravel the molecular network regulating insulin secretion. Here we performed a chemical screen and identified AZD7762, a compound that potentiates glucose-stimulated insulin secretion (GSIS) of a human β cell line, healthy and type 2 diabetic (T2D) human islets and primary cynomolgus macaque islets. In vivo studies in diabetic mouse models and cynomolgus macaques demonstrated that AZD7762 enhances GSIS and improves glucose tolerance. Furthermore, genetic manipulation confirmed that ablation of CHEK2 in human β cells results in increased insulin secretion. Consistently, high-fat-diet-fed Chk2−/− mice show elevated insulin secretion and improved glucose clearance. Finally, untargeted metabolic profiling demonstrated the key role of the CHEK2–PP2A–PLK1–G6PD–PPP pathway in insulin secretion. This study successfully identifies a previously unknown insulin secretion regulating pathway that is conserved across rodents, cynomolgus macaques and human β cells in both healthy and T2D conditions. (Figure presented.).
AB - After the discovery of insulin, a century ago, extensive work has been done to unravel the molecular network regulating insulin secretion. Here we performed a chemical screen and identified AZD7762, a compound that potentiates glucose-stimulated insulin secretion (GSIS) of a human β cell line, healthy and type 2 diabetic (T2D) human islets and primary cynomolgus macaque islets. In vivo studies in diabetic mouse models and cynomolgus macaques demonstrated that AZD7762 enhances GSIS and improves glucose tolerance. Furthermore, genetic manipulation confirmed that ablation of CHEK2 in human β cells results in increased insulin secretion. Consistently, high-fat-diet-fed Chk2−/− mice show elevated insulin secretion and improved glucose clearance. Finally, untargeted metabolic profiling demonstrated the key role of the CHEK2–PP2A–PLK1–G6PD–PPP pathway in insulin secretion. This study successfully identifies a previously unknown insulin secretion regulating pathway that is conserved across rodents, cynomolgus macaques and human β cells in both healthy and T2D conditions. (Figure presented.).
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U2 - 10.1038/s41589-023-01466-4
DO - 10.1038/s41589-023-01466-4
M3 - Article
C2 - 37945898
AN - SCOPUS:85176279767
SN - 1552-4450
VL - 20
SP - 566
EP - 576
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 5
ER -