| Literature DB >> 27341475 |
M Nagaya1, H Matsunari1, T Kanai2, M Maehara2, K Nakano1, I Umeki2, Y Katsumata2, Y Kasai2, R Sakai2, M Kobayashi2, M Honda1, N Abe2, M Watanabe1, K Umeyama1, H Nagashima1.
Abstract
The present study aimed at establishing a new cryopreservation method for mouse pancreatic islets by vitrification using hollow fibers as a container. A unique feature of the hollow fiber vitrification (HFV) method is that this method achieves stable vitrification using a minimum volume of cryoprotectant (CPA) solution, thereby ensuring high viability of the islets. The cytotoxicity, optimum composition, and concentration of the CPAs for vitrifying islets were examined. The viability, functional-integrity of vitrified islets were evaluated in comparison with those vitrified by conventional methods. Insulin secretion was measured in vitro by a static incubation assay and the metabolic functions was tested after transplantation into Streptozotocin-induced diabetic mice. The combination of 15% dimethyl sulfoxide+15% ethylene glycol resulted in the best CPA solution for the HFV of islets. HFV showed the highest viability in comparison to 2 vitrification methods, open pulled straws and vitrification with EDT324 solution. The vitrified islets stably expressed β-cells markers NeuroD, Pancreatic and duodenal homeobox-1, and MafA. Transplantation of the vitrified islets achieved euglycemia of the host diabetic mice and response to an intraperitoneal glucose tolerance test to a similar extent as non-vitrified transplanted islets. The HFV method allows for efficient long-term cryopreservation of islets. © Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2016 PMID: 27341475 DOI: 10.1055/s-0042-102628
Source DB: PubMed Journal: Horm Metab Res ISSN: 0018-5043 Impact factor: 2.936