Islet yield after different methods of pancreatic Liberase delivery

被引:10
作者
Andrades, P. [1 ]
Asiedu, C. [1 ]
Ray, P. [1 ]
Rodriguez, C. [1 ]
Goodwin, J. [1 ]
McCarn, J. [1 ]
Thomas, J. M. [1 ]
机构
[1] Univ Alabama, Dept Surg, Div Transplant Immunol, Birmingham, AL 35294 USA
关键词
D O I
10.1016/j.transproceed.2006.10.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective. Enzymatic digestion of the pancreas is a fundamental step in islet isolation and there are many ways to administer the enzyme during procurement. The aim of this study was to evaluate the influence of different methods of Liberase delivery during pancreas harvest on the quality and quantity of islets. Methods. Depending on the type of Liberase delivery, 4 groups were created. Group I was intraductal, Group 2 was interstitial, Group 3 was intragallbladder, and Group 4 was no infusion of enzyme. After injection, the pancreata were harvested, digested in Liberase solution, mechanically disrupted, and purified using discontinuous gradient centrifugation. After 24-hour culture, the number, purity, and viability of the isolated islets were determined. Results. Intraductal injection of the enzyme yielded statistically significantly more islets per mouse when compared with interstitial, intragal Hadder, and no injection administration. Although there was a trend toward better islet purity and viability for Group 1, this was not statistically significant. Conclusion. Intraductal administration is the best enzyme delivery method for pancreatic islet isolation. The pancreatic ducts are the most anatomic and physiological way to transport the enzyme uniformly inside the pancreas, determining an adequate digestion and better islet quantity and quality when compared with other delivery methods.
引用
收藏
页码:183 / 184
页数:2
相关论文
共 8 条
[1]   PREPARATION OF VIABLE ISLET CELLS FROM DOGS BY A NEW METHOD [J].
HORAGUCHI, A ;
MERRELL, RC .
DIABETES, 1981, 30 (05) :455-458
[2]   Pancreatic islets isolation using different protocols with in situ flushing and intraductal collagenase injection [J].
Kinasiewicz, A ;
Juszczak, M ;
Pachecka, J ;
Fiedor, P .
PHYSIOLOGICAL RESEARCH, 2004, 53 (03) :327-333
[3]   METHOD FOR ISOLATION OF INTACT ISLETS OF LANGERHANS FROM RAT PANCREAS [J].
LACY, PE ;
KOSTIANOVSKY, M .
DIABETES, 1967, 16 (01) :35-+
[4]   Intraductal collagenase delivery into the human pancreas using syringe loading or controlled perfusion [J].
Lakey, JRT ;
Warnock, GL ;
Shapiro, AMJ ;
Korbutt, GS ;
Ao, ZL ;
Kneteman, NM ;
Rajotte, RV .
CELL TRANSPLANTATION, 1999, 8 (03) :285-292
[5]   ISOLATION AND CULTURE OF ISLETS OF LANGERHANS OF GUINEA PIG [J].
MOSKALEW.S .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 1965, 5 (03) :342-+
[6]   IMPROVEMENT IN ISLET YIELD FROM A COLD-PRESERVED PANCREAS BY PANCREATIC DUCTAL COLLAGENASE DISTENSION AT THE TIME OF HARVESTING [J].
OHZATO, H ;
GOTOH, M ;
MONDEN, M ;
DONO, K ;
KANAI, T ;
MORI, T .
TRANSPLANTATION, 1991, 51 (03) :566-570
[7]  
SOCCI C, 1993, TRANSPLANTATION, V55, P661
[8]   Successful reversal of streptozotocin-induced diabetes with stable allogeneic islet function in a preclinical model of type 1 diabetes [J].
Thomas, JM ;
Contreras, JL ;
Smyth, CA ;
Lobashevsky, A ;
Jenkins, S ;
Hubbard, WJ ;
Eckhoff, DE ;
Stavrou, S ;
Neville, DM ;
Thomas, FT .
DIABETES, 2001, 50 (06) :1227-1236