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This fat-covered islet transplantation method is suitable for the detection of engrafted islets in the intraperitoneal cavity. Notably, it does not require the use of biobinding agents or suturing.
Islet transplantation is a cellular replacement therapy for severe diabetes mellitus. The intraperitoneal cavity is typically the transplant site for this procedure. However, intraperitoneal islet transplantation has some limitations, including poor transplant efficacy, difficult graft detection ability, and a lack of graftectomy capability for post-transplant analysis. In this paper, "fat-covered islet transplantation", an intraperitoneal islet transplantation method that utilizes epididymal white adipose tissue, is used to assess the therapeutic effects of bioengineered islets. The simplicity of the method lies in the seeding of islets onto epididymal white adipose tissue and using the tissue to cover the islets. While this method can be categorized as an intraperitoneal islet transplantation technique, it shares characteristics with intra-adipose tissue islet transplantation. The fat-covered islet transplantation method demonstrates more robust therapeutic effects than intra-adipose tissue islet transplantation, however, including the improvement of blood glucose and plasma insulin levels and the potential for graft removal. We recommend the adoption of this method for assessing the mechanisms of islet engraftment into white adipose tissue and the therapeutic effects of bioengineered islets.
Islet transplantation is a cellular replacement therapy for patients with severe diabetes mellitus. Recent reports have shown that rates of insulin-independence at three years after transplantation improve up to 44%1 and that approximately 80% of recipients who receive more than 600,000 total islet equivalents achieve insulin independence2. Furthermore, in the most recent Collaborative Islet Transplant Registry report, it was revealed that fasting blood glucose levels were maintained at 60-140 mg/dL for over a period of 5 years in over 70% of patients who underwent islet transplant alone. The study also determined that a....
The following procedure is performed in three steps. The first step includes the induction of diabetes in the recipient mice and the isolation of donor islets. The second step involves the preparation of islets before transplantation. In the third step, islet transplantation onto epididymal adipose tissue and covering of the islets using the adipose tissue is performed. After that, the therapeutic effects were assessed. The handling of the mice and the experimental procedures performed in this study comply with the ''Principles of Laboratory Animal Care'' (Guide for the Care and Use of Laboratory Animals, National Institutes of Health publication 8
To compare the transplant efficacy of fat-covered islet transplantation to that after intraperitoneal islet transplantation, the same number of islets was implanted onto the peritoneum at the left paracolic space of control recipient diabetic animals. The blood glucose levels of mice with fat-covered islet transplantation were observed to gradually and significantly decrease compared to intraperitoneal islet transplanted mice (p = 0.0023; Figure 3A). One month after transplantation, the bloo.......
The fat-covered islet transplantation method incorporates techniques from two different transplant techniques: intraperitoneal islet transplantation and intra-adipose tissue islet transplantation. As the surface membrane of epididymal white adipose tissue is considered to be the white adipose tissue that is covered by the peritoneum and that is attached to the epididymis, the fat-covered islet transplantation method can be anatomically categorized as a type of intraperitoneal islet transplantation. The technique by which.......
We have no conflict of interests.
This study was funded by a Grant-in-Aid for Scientific Research (C) (19K09839, NS) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
....Name | Company | Catalog Number | Comments |
4-0 Nylon | Alfresa | ER2004NA45-KF2 | Closing abdomen |
Alexa 488-conjugated donkey anti-guinea pig | Jackson Immunoresearch | 706-546-148 | Secondary antibody for insulin antibody |
Alexa 647-conjugated donkey anti-rabbit | Jackson Immunoresearch | 711-606-152 | Secondary antibody for von Willebrand factor antibody |
DMEM, low glucose, pyruvate | ThermoFisher Scientific | 11885084 | Culturing islets, transplanting islets |
Eosin | Fujifilm Wako Chemicals | 051-06515 | Using for staining tissue by eosin |
Eppendorf Safe-Lock Tubes, 1.5 mL | Eppendorf | 30120086 | Collecting islets |
Falcon 15 mL Conical Centrifuge Tubes | Corning | 352095 | Collecting islets |
Falcon 40 µm Cell Strainer | Falcon | 352340 | Using for separating islets from other pancreatic tissue |
Falcon 50 mL Conical Centrifuge Tubes | Corning | 352070 | Discarding excessive medium/buffer |
Guinea pig anti-insulin | Agilent Technologies Japan, Ltd. (Dako) | IR002 | Primary antibody for murine insulin |
Hematoxylin | Muto Pure Chemicals Co., Ltd. | 30002 | Using for staining tissue by hematoxylin |
Isodine solution 10% | Shionogi&Co., Ltd. | no catalog number | Using for disinfection |
Isoflurane | Fujifilm Wako Chemicals | 095-06573 | Using for anesthesia |
Labcon 1000 µL ZapSilk Low Retention Pipette Tips | Labcon | 1177-965-008 | Using for separating islets from other pancreatic tissue |
Labcon 200 µL ZapSilk Low Retention Pipette Tips | Labcon | 1179-965-008 | Using for seeding islets onto epididymal white adipose tissue |
Mintsensor | Sanwa Kagaku Kenkyusho Co. Ltd., | 8AEB02E | Using for monitoring blood glucose |
Pipetteman P-1000 | Gilson | F123602 | Using for separating islets from other pancreatic tissue |
Pipetteman P-200 | Gilson | F123601 | Using for seeding islets onto epididymal white adipose tissue |
Rabbit anti-vWF | Abcam | ab6994 | Primary antibody for murine von Willebrand factor |
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