Experimental study of a modified extraction method of mouse islets
10.3969/j.issn.1674-7445.2020.05.007
- VernacularTitle:小鼠胰岛提取方法改良的实验研究
- Author:
Wen ZENG
1
;
Kunying LIU
;
Chuwen LIN
;
Shuo LIN
;
Hangya PENG
;
Haicheng LI
;
Longyi ZENG
Author Information
1. Department of Endocrinology and Metabolic Diseases, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China
- Publication Type:Research Article
- Keywords:
Islet;
Islet transplantation;
Common bile duct puncture;
In situ injection;
Insulin;
Glucagon;
Collagenase P;
Dithizone
- From:
Organ Transplantation
2020;11(5):572-
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the improvement and effect of the method of islet extraction in mice. Methods According to different islet extraction methods, all mice were randomly divided into the common bile duct puncture group (n=100) and common bile duct puncture combined with in situ pancreatic injection group (combined injection group, n=100). Common bile duct puncture combined with in situ pancreatic injection was utilized as the modified method. The islets were selected and purified under stereomicroscope. The morphology and purification of islets were identified. The islet yield and success rate of islet extraction were statistically compared between two groups. The survival of islets after 1 week culture in vitro was analyzed, and the insulin secretion function of islets after 24 h and 4 d culture in vitro was evaluated. Results Compared with the common bile duct puncture group, the islet yield in the combined injection group was significantly increased (P < 0.001). The success rate of islet extraction in both groups was 83% with no statistical significance (P > 0.05). The islets extracted by common bile duct puncture combined with in situ pancreatic injection had intact morphology, high purity and high activity. The survival rate of newly isolated islets was nearly 100% after 24 h culture in vitro. After 1~5 d culture in vitro, the islet cells survived well. After 6 d culture in vitro, the islets showed central death. After culture in vitro for 24 h and 4 d, the islet function of the mice was normal after high glucose stimulation. Conclusions Common bile duct puncture combined with in situ pancreatic injection can increase the islet yield, and the obtained islet cells have high activity and proper function.
