共 38 条
Effect of Transplantation of Mesenchymal Stem Cells Induced into Early Hepatic Cells in Streptozotocin-Induced Diabetic Mice
被引:7
作者:

Dinarvand, Peyman
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h-index: 0
机构:
Stem Cell Technol Res Ctr, Dept Stem Cells & Tissue Engn, Tehran 141553117, Iran Tarbiat Modares Univ, Dept Hematol, Fac Med Sci, Tehran 14115111, Iran

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机构:
[1] Tarbiat Modares Univ, Dept Hematol, Fac Med Sci, Tehran 14115111, Iran
[2] Stem Cell Technol Res Ctr, Dept Stem Cells & Tissue Engn, Tehran 141553117, Iran
[3] Tarbiat Modares Univ, Dept Immunol, Fac Med Sci, Tehran 14115111, Iran
关键词:
transplantation;
mesenchymal stem cell;
diabetic mouse;
early hepatic cell;
INSULIN-PRODUCING CELLS;
VITRO TRANS-DIFFERENTIATION;
MURINE BONE-MARROW;
CORD BLOOD-CELLS;
IN-VITRO;
MATURE HEPATOCYTES;
PROGENITOR CELLS;
STROMAL CELLS;
THERAPY;
HYPERGLYCEMIA;
D O I:
10.1248/bpb.33.1212
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Cellular replacement therapy for diabetes mellitus has received much attention. In this study we investigated the effect of transplantation of bone marrow-derived mesenchymal stem cells (BM-MSCs) induced into endoderm and early hepatic cells in streptozotocin (STZ)-induced diabetic mice. Mouse BM-MSCs were cultured in the presence of hepatocyte growth factor (HGF) and fibroblast growth factor (FGF-4) for 2 weeks and transplanted into diabetic mice. Blood glucose levels, intraperitoneal glucose tolerance test, serum insulin, body weight and islets histology were analyzed. The results demonstrated that transplantation of syngeneic induced MSCs could reverse STZ-induced diabetes in mice. The treatment of mice with hyperglycemia and islet destruction resulted in the repair of pancreatic islets. Blood glucose levels, intraperitoneal glucose tolerance test, and serum insulin were significantly recovered in induced BM-MSCs (iBM-MSCs) group. In addition, in the iBM-MSCs group the body weight and the number of islets were significantly increased compared to other groups. The results demonstrate that BM-MSCs induced into endoderm and early hepatic cells are suitable candidates for cell-based therapy of diabetes mellitus.
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页码:1212 / 1217
页数:6
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