Factors influencing isolation of functional pancreatic rat islets

被引:29
作者
de Haan, BJ [1 ]
Faas, MM [1 ]
Spijker, H [1 ]
van Willigen, JW [1 ]
de Haan, A [1 ]
de Vos, P [1 ]
机构
[1] Univ Groningen, Sect Med Biol, NL-9700 RB Groningen, Netherlands
关键词
islets; transplantation; bovine serum albumin; rat; strain; collagenase;
D O I
10.1097/00006676-200407000-00063
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Yields and function of isolated islets vary considerably in spite of the introduction of new or improved methods for isolation. In most studies. these variations have been attributed to inadequacies of the applied collagenase preparations. However, when we retrospectively analyzed our rat islet isolations, we found large variations in yield and function in spite of application of identical collagenase sources. Therefore, in the present study, we determined the effect of rat donor strain, the source of inhibition of proteolytic activity (by bovine serum albumin). and the culture conditions on yield and function. AO rats showed a twofold higher islet yield than Wistar and Lewis rats. However, a higher yield was not associated with a higher response on glucose load since this response was more pronounced with Lewis islets than with Wistar and AO islets. Rats with a higher weight donate more islets but have a lower insulin secretory capacity. Islet yield and function also vary with application of different sources of bovine serum albumin during digestion, Moreover, the culture conditions influence the functional survival of isolated rat islets. CMRL 1066 preserves the insulin secretory capacity of rat islets better than RPMI 1640. Finally, the number of islets surviving the culture is higher when 4 instead of 12 and 24 islets were applied per square centimeter. Our observations indicate that strain and weight of the rat donor, the source of bovine serum albumin, and the culture conditions of islets are pertinent factors in efficacious isolation of islets.
引用
收藏
页码:E15 / E22
页数:15
相关论文
共 33 条
[1]   ULTRAVIOLET-LIGHT IRRADIATION REDUCES HUMAN ISLET IMMUNOGENICITY WITHOUT ALTERING ISLET FUNCTION [J].
BENHAMOU, PY ;
STEIN, E ;
HOBER, C ;
MIYAMOTO, M ;
WATANABE, Y ;
NOMURA, Y ;
WATT, PC ;
KENMOCHI, T ;
BRUNICARDI, FC ;
MULLEN, Y .
HORMONE AND METABOLIC RESEARCH, 1995, 27 (03) :113-120
[2]  
BERGSTEN P, 1994, J BIOL CHEM, V269, P1041
[3]  
Cerasi E, 1997, DIABETES METAB, V23, P47
[4]   Survival and function of islets during culture [J].
Clayton, HA ;
London, NJM .
CELL TRANSPLANTATION, 1996, 5 (01) :1-12
[5]   GLUCOSE COUNTERREGULATION - PREVENTION AND CORRECTION OF HYPOGLYCEMIA IN HUMANS [J].
CRYER, PE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02) :E149-E155
[6]   Considerations for successful transplantation of encapsulated pancreatic islets [J].
de Vos, P ;
Hamel, AF ;
Tatarkiewicz, K .
DIABETOLOGIA, 2002, 45 (02) :159-173
[7]  
DEGRAAFF MPA, 1994, TRANSPLANT P, V26, P1171
[8]  
FALQUI L, 1991, TRANSPLANTATION, V51, P1322
[9]   ISLET TRANSPLANTATION - THE CONNECTION OF EXPERIMENT AND CLINIC EXEMPLIFIED BY THE TRANSPLANTATION OF ISLETS OF LANGERHANS [J].
FEDERLIN, KF .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY, 1993, 101 (06) :334-345
[10]   EFFECT OF ALGINATE-POLYLYSINE-ALGINATE MICROENCAPSULATION ON INVITRO INSULIN RELEASE FROM RAT PANCREATIC-ISLETS [J].
FRITSCHY, WM ;
WOLTERS, GHJ ;
VANSCHILFGAARDE, R .
DIABETES, 1991, 40 (01) :37-43