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人胰岛分离:第一部分:胰腺组织的消化与采集。

Human pancreatic islet isolation: Part I: digestion and collection of pancreatic tissue.

作者信息

Qi Meirigeng, Barbaro Barbara, Wang Shusen, Wang Yong, Hansen Mike, Oberholzer Jose

机构信息

Department of Surgery, University of Illinois, Chicago, IL, USA.

出版信息

J Vis Exp. 2009 May 26(27):1125. doi: 10.3791/1125.

Abstract

Management of Type 1 diabetes is burdensome, both to the individual and society, costing over 100 billion dollars annually. Despite the widespread use of glucose monitoring and new insulin formulations, many individuals still develop devastating secondary complications. Pancreatic islet transplantation can restore near normal glucose control in diabetic patients, without the risk of serious hypoglycemic episodes that are associated with intensive insulin therapy. Providing sufficient islet mass is important for successful islet transplantation. However, donor characteristic, organ procurement and preservation affect the isolation outcome. At University of Illinois at Chicago (UIC) we have developed a successful isolation protocol with an improved purification gradient. The program started in January 2004, and more than 300 isolations were performed up to November 2008. The pancreata were sent in cold preservation solutions (UW, University of Wisconsin or HTK, Histidine-Tryptophan Ketoglutarate) to the Cell Isolation Laboratory at UIC for islet isolation. Pancreatic islets were isolated using the UIC method, which is a modified version of the method originally described by Ricordi et al. Briefly, after cleaning the pancreas from the surrounding tissue, it was perfused with enzyme solution (Serva Collagenase + Neutral Protease or Sigma V enzyme). The distended pancreas was then transferred to the Ricordi digestion chamber, connected to a modified, closed circulation tubing system, and warmed up to 37 degrees C. During the digestion, the chamber was shaken gently. Samples were taken continuously to monitor the digestion progress. Once free islets were detected under the microscope, the digestion was stopped by flushing cold (4 degrees C) RPMI dilution solution (Mediatech, Herndon, VA) into the circulation system to dilute the enzyme. After being collected and washed in M199 media supplemented with human albumin, the tissue was sampled for pre-purification count and incubated with UW solution before purification. Purification process will be described in Part II: Purification and Culture of Human Islets.

摘要

1型糖尿病的管理对个人和社会而言都负担沉重,每年花费超过1000亿美元。尽管葡萄糖监测和新型胰岛素制剂得到广泛应用,但许多患者仍会出现严重的继发性并发症。胰岛移植能够使糖尿病患者的血糖控制恢复到接近正常水平,且不存在强化胰岛素治疗相关的严重低血糖发作风险。提供足够的胰岛数量对于胰岛移植的成功至关重要。然而,供体特征、器官获取和保存会影响分离结果。在伊利诺伊大学芝加哥分校(UIC),我们开发了一种成功的分离方案,采用了改进的纯化梯度。该项目于2004年1月启动,截至2008年11月已进行了300多次分离。胰腺在冷保存溶液(UW,威斯康星大学溶液或HTK,组氨酸 - 色氨酸 - 酮戊二酸溶液)中被送往UIC的细胞分离实验室进行胰岛分离。胰岛采用UIC方法进行分离,该方法是对Ricordi等人最初描述的方法的改良版本。简要来说,在清除胰腺周围组织后,用酶溶液(Serva胶原酶 + 中性蛋白酶或Sigma V酶)进行灌注。然后将膨胀的胰腺转移到Ricordi消化室,连接到改良的封闭循环管道系统,并加热至37摄氏度。在消化过程中,轻轻摇晃消化室。持续取样以监测消化进程。一旦在显微镜下检测到游离胰岛,通过将冷(4摄氏度)RPMI稀释溶液(Mediatech,弗吉尼亚州赫恩登)冲入循环系统以稀释酶来停止消化。在收集并在补充有人白蛋白的M199培养基中洗涤后,对组织进行预纯化计数取样,并在纯化前用UW溶液孵育。纯化过程将在第二部分:人胰岛的纯化和培养中描述。

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