R-spondin1 deficiency enhances β-Cell neogenesis in a murine model of diabetes

Pancreas. 2014 Jan;43(1):93-102. doi: 10.1097/MPA.0b013e3182a70bfb.

Abstract

Objective: The cWnt activator, R-spondin1 (Rspo1), regulates β-cell growth, function, and neogenesis, although its role in conditions such as streptozotocin (STZ)-induced diabetes is unknown. We hypothesized that Rspo1 deficiency enhances β-cell neogenesis in STZ-induced diabetes.

Methods: Wild-type (Rspo1) and knockout (Rspo1) mice were injected with STZ (40 mg/kg) for 5 days, followed by analysis of oral glucose and insulin tolerance, and were killed on day 6 (acute; 9-11 mice) or 32 (chronic; 11-16 mice). Immunohistochemistry was performed for β-cell apoptosis, proliferation, neogenesis, and markers of β-cell maturity.

Results: There was no difference in oral glucose handling between STZ-induced Rspo1 and Rspo1 mice, although Rspo1 mice demonstrated increased insulin sensitivity. β-cell mass, islet number, and islet size distribution did not differ between STZ-induced Rspo1 and Rspo1 mice, but Rspo1 animals had reduced β-cell apoptosis and increased numbers of insulin-positive ductal cells, indicating β-cell neogenesis. Furthermore, the increased β-cell regeneration observed in the Rspo1 animals was associated with a more differentiated/mature β-cell phenotype as assessed by increased immunopositivity for Nkx6.1, MafA, and GLUT2.

Conclusions: These findings indicate that Rspo1 is a negative regulator of β-cell neogenesis, development, and survival in the face of STZ-induced diabetes, providing a therapeutic target for the enhancement of β-cell mass.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Cell Count
  • Cell Proliferation
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / physiopathology*
  • Female
  • Glucose Transporter Type 2 / metabolism
  • Homeodomain Proteins / metabolism
  • Immunohistochemistry
  • Insulin / genetics
  • Insulin / metabolism
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / physiology*
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / physiopathology*
  • Maf Transcription Factors, Large / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Regeneration
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thrombospondins / deficiency*
  • Thrombospondins / genetics
  • Thrombospondins / metabolism

Substances

  • Glucose Transporter Type 2
  • Homeodomain Proteins
  • Ins2 protein, mouse
  • Insulin
  • Maf Transcription Factors, Large
  • Mafa protein, mouse
  • Nkx6-1 protein, mouse
  • RSPO1 protein, mouse
  • Slc2a2 protein, mouse
  • Thrombospondins