Treating diet-induced diabetes and obesity with human embryonic stem cell-derived pancreatic progenitor cells and antidiabetic drugs

Stem Cell Reports. 2015 Apr 14;4(4):605-20. doi: 10.1016/j.stemcr.2015.02.011. Epub 2015 Mar 19.

Abstract

Human embryonic stem cell (hESC)-derived pancreatic progenitor cells effectively reverse hyperglycemia in rodent models of type 1 diabetes, but their capacity to treat type 2 diabetes has not been reported. An immunodeficient model of type 2 diabetes was generated by high-fat diet (HFD) feeding in SCID-beige mice. Exposure to HFDs did not impact the maturation of macroencapsulated pancreatic progenitor cells into glucose-responsive insulin-secreting cells following transplantation, and the cell therapy improved glucose tolerance in HFD-fed transplant recipients after 24 weeks. However, since diet-induced hyperglycemia and obesity were not fully ameliorated by transplantation alone, a second cohort of HFD-fed mice was treated with pancreatic progenitor cells combined with one of three antidiabetic drugs. All combination therapies rapidly improved body weight and co-treatment with either sitagliptin or metformin improved hyperglycemia after only 12 weeks. Therefore, a stem cell-based therapy may be effective for treating type 2 diabetes, particularly in combination with antidiabetic drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation*
  • Cell- and Tissue-Based Therapy
  • Diabetes Mellitus, Type 2 / etiology*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / therapy
  • Diet / adverse effects*
  • Diet, High-Fat / adverse effects
  • Disease Models, Animal
  • Gene Expression Profiling
  • Glucose / metabolism
  • Human Embryonic Stem Cells / cytology*
  • Humans
  • Hyperglycemia
  • Hypoglycemic Agents / pharmacology*
  • Insulin Resistance
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / metabolism
  • Islets of Langerhans / cytology
  • Liver / anatomy & histology
  • Liver / metabolism
  • Mice
  • Mice, SCID
  • Obesity / etiology*
  • Obesity / metabolism
  • Obesity / therapy
  • Organ Size
  • Pancreas / cytology*
  • Phenotype
  • Stem Cell Transplantation*
  • Stem Cells / cytology*

Substances

  • Hypoglycemic Agents
  • Glucose