Soluble T-cadherin secretion from endothelial cells is regulated via insulin/PI3K/Akt signalling

Biochem Biophys Res Commun. 2024 Nov 5:732:150403. doi: 10.1016/j.bbrc.2024.150403. Epub 2024 Jul 14.

Abstract

Aim and objective: Our recent report showed that soluble T-cadherin promotes pancreatic beta-cell proliferation. However, how and where the secretion of soluble T-cadherin is regulated remain unclear.

Methods and results: Soluble T-cadherin levels significantly increased in leptin receptor-deficient db/db mice with hypoinsulinaemia or in wild-type mice treated with insulin receptor blockade by S961. Similar results were observed in human subjects; Diabetic ketoacidosis patients at the time of hospitalization had increased plasma soluble T-cadherin levels, which decreased after insulin infusion therapy. Patients with recurrent ovarian cancer who were administered a phosphatidylinositol-3 kinase (PI3K)-alpha inhibitor (a new anticancer drug) had increased plasma soluble T-cadherin and plasma C-peptide levels. Endothelial cell-specific T-cadherin knockout mice, but not skeletal muscle- or cardiac muscle-specific T-cadherin knockout mice, showed a 26 % reduction in plasma soluble T-cadherin levels and a significant increase in blood glucose levels in streptozocin-induced diabetes. The secretion of soluble T-cadherin from human endothelial cells was approximately 20 % decreased by insulin and this decrease was canceled by blockade of insulin receptor/Akt signalling, not Erk signalling.

Conclusion: We conclude that insulin regulates soluble T-cadherin levels and soluble T-cadherin secretion from endothelial cells is positively regulated by insulin/insulin receptor/Akt signalling.

Keywords: Endothelial cells; Insulin demand; Insulin signalling; soluble T-cadherin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins* / metabolism
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Female
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Insulin* / blood
  • Insulin* / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Peptides
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Receptor, Insulin / metabolism
  • Receptors, Leptin / genetics
  • Receptors, Leptin / metabolism
  • Signal Transduction*

Substances

  • H-cadherin
  • Cadherins
  • Proto-Oncogene Proteins c-akt
  • Insulin
  • Phosphatidylinositol 3-Kinases
  • Receptor, Insulin
  • S961 peptide
  • Receptors, Leptin
  • Peptides