Table 1.
Types | Routes of transplantation | Outcome |
Human MSCs | Intravenously introduced to Non-obese diabetic/Severe combined immunodeficiency mice with total body irradiation or local abdominal or leg irradiation | Safe and efficient for the long-term treatment of severe complication after radiotherapy[46] |
Umbilical cord derived MSCs | Injected directly into the pancreas | Improvement of metabolic control. Enhancement of islet engraftment and survival[42] |
Bone marrow-derived MSC | Differentiated in vivo into functioning β-cells | Normalization of chronic hyperglycemia in a diabetic rat[47] |
Human placenta ‑derived MSCs | Differentiated into islet-like cell clusters and transplanted into streptozocin-induced diabetic mice | Restoration of normoglycemia in diabetic mice[48] |
Human umbilical cord blood derived MSCs | Differentiated into IPC through intravenous administration | Improvement in glycemic profiles, histological improvement of insulates[49] |
Wharton's jelly and amniotic membrane derived MSCs | (1) Differentiated into IPC and transplanted into the liver; (2) Infected with PDX1 gene and differentiated to IPC; and (3) Differentiated into IPC and transplanted into the liver of STZ-induced diabetic rats | Expression of insulin Secretion of C-peptide; expression of pancreas-specific genes[49]; correspondence to high concentrations of glucose[50]; reduction of blood glucose levels after 4 wk of transplantation[51] |
MSCs: Mesenchymal stem cells; IPC: Insulin-producing cells.