玻璃化
小岛
胰岛
化学
生物医学工程
生物
男科
材料科学
计算生物学
医学
内分泌学
胰岛素
作者
Takahiro Yamanaka,Teppei Goto,Masumi Hirabayashi,Shinichi Hochi
出处
期刊:Biopreservation and Biobanking
[Mary Ann Liebert]
日期:2017-09-05
卷期号:15 (5): 457-462
被引量:12
标识
DOI:10.1089/bio.2017.0044
摘要
The practical requirements of islet transplantation necessitate that a large quantity of pancreatic islets be cryopreserved for a long period of time in a simple and convenient manner. We cryopreserved rat islets (size range 101-150 μm in mean diameter) by vitrification with either a Cryotop® device or a ø = 57-μm nylon mesh device in units of 10 islets, or by conventional freezing with a Bicell® vessel in units of 50 islets. Postwarm/thaw survival rates of the islets were 68.1% ± 5.9%, 64.1% ± 3.5%, and 47.7 ± 1.2% following Cryotop vitrification, nylon mesh vitrification, and Bicell freezing, respectively (p < 0.05). Glucose-stimulated insulin secretion in the two vitrification groups (stimulus index [SI] = 3.1-3.9) was superior to that in the freezing group (SI = 0.8). Additional experiments involved scaling-up the cryopreservation process using the nylon mesh device in units of 10, 50, or 100 islets. Increased numbers of islets per device had no adverse effects on cryosurvival (58.6%-68.5%) or insulin secretion potential (SI = 2.8-4.2). As the nylon mesh device does not require the handling of individual islets with glass pipettes, pre- and postvitrification islet treatment is less complicated. Therefore, nylon mesh can serve as a simple cryodevice for the vitrification of large quantities of rat pancreatic islets.
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