TRANSPLANTATION OF BETA-CELLS FROM TRANSGENIC MICE INTO NUDE ATHYMIC DIABETIC RATS RESTORES GLUCOSE REGULATION

被引:12
作者
HICKS, BA
STEIN, R
EFRAT, S
GRANT, S
HANAHAN, D
DEMETRIOU, AA
机构
[1] VANDERBILT UNIV,VET ADM MED CTR,SCH MED,DEPT SURG,A-2219 MCN,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,VET ADM MED CTR,SCH MED,DEPT MOLEC PHYSIOL,NASHVILLE,TN 37232
[3] VANDERBILT UNIV,VET ADM MED CTR,SCH MED,DEPT BIOPHYS,NASHVILLE,TN 37232
[4] COLD SPRING HARBOR LAB,COLD SPRING HARBOR,NY 11724
关键词
BETA-CELL TRANSPLANTATION; STREPTOZOTOCIN INDUCED DIABETES; INSULIN-DEPENDENT DIABETES-MELLITUS; CELL THERAPY; RAT;
D O I
10.1016/0168-8227(91)90016-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have shown that elevated plasma D-glucose levels in experimentally-induced diabetic nude athymic rats can be reduced by intraperitoneal transplantation of microcarrier-attached insulin producing beta-cells from the mouse pancreatic beta-cell line, beta-TC-1. The reduction in the level of hyperglycemia was observed as early as two days following cell transplantation and was associated with a concomitant increase in plasma insulin levels. beta-TC-1 cell transplanted diabetic rats had plasma D-glucose levels similar to those found in non-diabetic control animals and remained normoglycemic throughout the 39 day experimental period. The beta-TC-1 cell transplanted diabetic rats also had near normalization of body weight, food and water intake and of urine output when compared to control diabetic and non-diabetic rats. Similarly, they exhibited improved blood glucose clearance following intravenous D-glucose administration. These results suggest that beta-TC-1 cells regulate D-glucose homeostasis following transplantation into diabetic rat recipients in a manner similar to that of endogenous pancreatic beta-cells.
引用
收藏
页码:157 / 164
页数:8
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