Combinatorial treatment of bone marrow stem cells and stromal cell-derived factor 1 improves glycemia and insulin production in diabetic mice

被引:4
作者
Cheng, H. [1 ]
Zhang, Y. C. [2 ]
Wolfe, S. [2 ]
Valencia, V. [2 ]
Qian, K. [2 ]
Shen, L. [2 ]
Tang, Y. L. [3 ]
Hsu, W. H. [4 ]
Atkinson, M. A. [5 ]
Phillips, M. I. [3 ]
机构
[1] Louisiana State Univ, Sch Vet Med, Dept Comparat Biomed Sci, Baton Rouge, LA 70803 USA
[2] Univ S Florida, Dept Pediat, Childrens Res Inst, Petersburg, FL USA
[3] Keck Grad Inst, Claremont, CA USA
[4] Iowa State Univ, Coll Vet Med, Dept Biomed Sci, Ames, IA USA
[5] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
关键词
Bone marrow stem cells; Homing; SDF-1; Insulin; Diabetes; Liver; PANCREATIC BETA-CELLS; IN-VITRO; CHEMOKINE RECEPTORS; ENDOTHELIAL-CELLS; PROGENITOR CELLS; EX-VIVO; DIFFERENTIATION; EXPRESSION; MIGRATION; ISLETS;
D O I
10.1016/j.mce.2011.07.024
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Transdifferentiation of stem cells into insulin-producing cells for the treatment of diabetes have shown promising but inconsistent results. We examined the potential for attracting bone marrow stem cells (BMSCs) to the pancreas using a chemokine, stromal cell-derived factor 1 (SDF-1). SDF-1 treatment markedly increased the number of GFP labeled BMSCs in the pancreas, but surprisingly, the majority was observed in liver. The liver cells had typical pancreatic endocrine cell gene expression including insulin 1, insulin II, PDX-1, somatostatin, and glucagon. Combined treatment with SDF-1 and BMSC transplant reduced hyperglycemia and prolonged the long-term survival of diabetic mice, and a sub group had complete normoglycemia (<150 mg/dl), restored blood insulin levels, and normal glucose tolerance. Our results suggest that SDF-1 could potentially be used to improve the homing of stem cells and beta-cell regeneration. The mechanism appears to involve an increase in insulin producing cells mainly in the liver. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:88 / 96
页数:9
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