Development of an ectopic site for islet transplantation, using biodegradable scaffolds

被引:77
作者
Dufour, JM
Rajotte, RV
Zimmerman, M
Rezania, A
Kin, T
Dixon, DE
Korbutt, GS [1 ]
机构
[1] Univ Alberta, Surg Med Res Inst, Dent Pharm Ctr 1074, Edmonton, AB T6G 2N8, Canada
[2] Univ Alberta, Dept Surg, Edmonton, AB T6G 2N8, Canada
[3] Univ Alberta, Dept Med, Edmonton, AB T6G 2N8, Canada
[4] LifeScan, Skillman, NJ USA
来源
TISSUE ENGINEERING | 2005年 / 11卷 / 9-10期
关键词
D O I
10.1089/ten.2005.11.1323
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Clinical islet transplantation in liver has achieved normoglycemia. However, this site may not be ideal for islet survival. To create a more optimal site for islet transplantation, we have developed a construct with biodegradable scaffolds. Islets were seeded in scaffolds and transplanted into the epididymal fat pad of diabetic BALB/c mice. Controls included islets transplanted underneath the kidney capsule or into the fat pad without scaffolds. All animals with islets in scaffolds or the kidney became normoglycemic and maintained this metabolic state. When islets were transplanted without scaffolds the time to achieve normoglycemia was significantly increased and less than 45% of mice survived. An oral glucose tolerance test was performed on the scaffold and kidney groups with similar blood glucose levels and area under the curve values between the groups. Grafts were removed at more than 100 days posttransplantation and all animals became hyperglycemic. There was no significant difference in insulin content between the grafts and all grafts were well vascularized with insulin-positive beta cells. Therefore, islets in scaffolds function and restore diabetic animals to normoglycemic levels, similar to islets transplanted underneath the kidney capsule, suggesting scaffolds can be used to create a site for islet transplantation.
引用
收藏
页码:1323 / 1331
页数:9
相关论文
共 30 条
[21]   Tissue engineering: Current state and prospects [J].
Stock, UA ;
Vacanti, JP .
ANNUAL REVIEW OF MEDICINE, 2001, 52 :443-451
[22]   Testicular Sertoli cells protect islet β-cells from autoimmune destruction in NOD mice by a transforming growth factor-β1-dependent mechanism [J].
Suarez-Pinzon, W ;
Korbutt, GS ;
Power, R ;
Hooton, J ;
Rajotte, RV ;
Rabinovitch, A .
DIABETES, 2000, 49 (11) :1810-1818
[23]   CHARACTERIZATION OF RAT TESTICULAR PERITUBULAR MYOID CELLS IN CULTURE - ALPHA-SMOOTH MUSCLE ISOACTIN IS A SPECIFIC DIFFERENTIATION MARKER [J].
TUNG, PS ;
FRITZ, IB .
BIOLOGY OF REPRODUCTION, 1990, 42 (02) :351-365
[24]   Maintenance of beta-cell function and survival following islet isolation requires re-establishment of the islet-matrix relationship [J].
Wang, RN ;
Rosenberg, L .
JOURNAL OF ENDOCRINOLOGY, 1999, 163 (02) :181-190
[25]  
WARNOCK GL, 1989, TRANSPLANT P, V21, P2617
[26]  
WARNOCK GL, 1990, HORM METAB RES, V25, P156
[27]  
WARNOCK GL, 1992, TRANSPLANT REV, V6, P195
[28]   Pancreas resection and islet autotransplantation for end-stage chronic pancreatitis [J].
White, SA ;
Davies, JE ;
Pollard, C ;
Swift, SM ;
Clayton, HA ;
Sutton, CD ;
Weymss-Holden, S ;
Musto, PP ;
Berry, DP ;
Dennison, AR .
ANNALS OF SURGERY, 2001, 233 (03) :423-431
[29]   The risks of total pancreatectomy and splenic islet autotransplantation [J].
White, SA ;
London, NJM ;
Johnson, PRV ;
Davies, JE ;
Pollard, C ;
Contractor, HH ;
Hughes, DP ;
Robertson, GSM ;
Musto, PP ;
Dennison, AR .
CELL TRANSPLANTATION, 2000, 9 (01) :19-24
[30]   A NEW SITE FOR ISLET TRANSPLANTATION - A PERITONEAL-OMENTAL POUCH [J].
YASUNAMI, Y ;
LACY, PE ;
FINKE, EH .
TRANSPLANTATION, 1983, 36 (02) :181-182