Checkpoint kinase 2 controls insulin secretion and glucose homeostasis

Nat Chem Biol. 2024 May;20(5):566-576. doi: 10.1038/s41589-023-01466-4. Epub 2023 Nov 9.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Cycle Proteins / metabolism
  • Checkpoint Kinase 2* / genetics
  • Checkpoint Kinase 2* / metabolism
  • Diabetes Mellitus, Type 2 / metabolism
  • Glucose* / metabolism
  • Homeostasis*
  • Humans
  • Insulin Secretion* / drug effects
  • Insulin* / metabolism
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism
  • Macaca fascicularis*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases* / genetics
  • Protein Serine-Threonine Kinases* / metabolism
  • Proto-Oncogene Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • Checkpoint Kinase 2
  • CHEK2 protein, human
  • Glucose
  • Insulin
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins
  • Chek2 protein, mouse