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低温胶原酶消化法用于从48小时冷保存的大鼠胰腺中分离胰岛。

Low temperature collagenase digestion for islet isolation from 48-hour cold-preserved rat pancreas.

作者信息

Dono K, Gotoh M, Monden M, Kanai T, Fukuzaki T, Mori T

机构信息

Department of Surgery II, Osaka University Medical School, Japan.

出版信息

Transplantation. 1994 Jan;57(1):22-6. doi: 10.1097/00007890-199401000-00005.

Abstract

We examined the efficacy of relatively low temperature collagenase digestion at 20 degrees C on the yield and viability of islets after long-term cold preservation. Wistar rat pancreases were distended with University of Wisconsin solution via a pancreatic duct at the time of harvesting to which collagenase and 2.5 mM calcium chloride were added. The pancreases were cold-preserved at 4 degrees C for 24 or 48 hr. After storage, they were incubated for collagenase digestion at 37 degrees C or 20 degrees C for various incubation periods to obtain the peak yield. At 20 degrees C, in vitro collagenase activity measured by the FALGPA method was one fourth of that at 37 degrees C, and pancreases were well digested with a prolonged digestion period (60-90 min vs. 15-20 min for the 37 degrees C group). In vitro insulin secretion of islets isolated from freshly removed pancreases was maintained at 20 degrees C for 120 min in University of Wisconsin solution as compared with 30 min at 37 degrees C. Therefore, the preserved pancreases used in this study were incubated either at 37 degrees C or 20 degrees C at various times in order to obtain peak islet yields. The islet yields from 24-hr cold-preserved pancreases at 37 degrees C and 20 degrees C digestion were 573 +/- 59/rat (n = 6) and 497 +/- 84/rat (n = 11), respectively, and those from 48-hr cold-preserved pancreases were 395 +/- 113/rat (n = 6) and 414 +/- 75/rat (n = 6), respectively. The yields from 24- and 48-hr cold-preserved pancreases were significantly low compared with 635 +/- 52/rat for fresh pancreases (n = 15), but there was no significant difference between the 2 methods. The viability of the isolated islets, which was examined by transplantation to streptozotocin-induced diabetic C57BL/6 mice, showed a significant difference in the capacity to ameliorate diabetes. The functional success rate of islet transplantation after 24-hr cold preservation was equally good (8/8 for 37 degrees C group vs. 9/10 for 20 degrees C group), but the rate for those from 48-hr cold-preserved pancreases was significantly better with digestion at 20 degrees C than at 37 degrees C (1/8 for 37 degrees C group vs. 7/8 for 20 degrees C group, P < 0.05). We concluded that viable islets can be isolated from 48-hr cold-preserved pancreases with the low temperature collagenase digestion method, which shows promise as a modality for successful clinical islet transplantation.

摘要

我们研究了20摄氏度相对低温的胶原酶消化法对长期冷藏后胰岛产量和活力的影响。在收获时,通过胰管向Wistar大鼠胰腺中注入威斯康星大学溶液,并添加胶原酶和2.5 mM氯化钙。胰腺在4摄氏度下冷藏24或48小时。储存后,将它们在37摄氏度或20摄氏度下孵育不同时间进行胶原酶消化以获得最高产量。在20摄氏度下,通过FALGPA法测得的体外胶原酶活性是37摄氏度下的四分之一,延长消化时间(60 - 90分钟,而37摄氏度组为15 - 20分钟)可使胰腺得到充分消化。与37摄氏度下30分钟相比,从新鲜取出的胰腺中分离的胰岛在20摄氏度的威斯康星大学溶液中体外胰岛素分泌可维持120分钟。因此,本研究中使用的保存胰腺在不同时间于37摄氏度或20摄氏度下孵育以获得最高胰岛产量。37摄氏度和20摄氏度消化的24小时冷藏胰腺的胰岛产量分别为573±59/只大鼠(n = 6)和497±84/只大鼠(n = 11),48小时冷藏胰腺的胰岛产量分别为395±113/只大鼠(n = 6)和414±75/只大鼠(n = 6)。与新鲜胰腺的635±52/只大鼠(n = 15)相比,24小时和48小时冷藏胰腺的产量显著较低,但两种方法之间无显著差异。通过移植到链脲佐菌素诱导的糖尿病C57BL/6小鼠中检测分离胰岛的活力,结果显示在改善糖尿病的能力上存在显著差异。24小时冷藏后胰岛移植的功能成功率相当(37摄氏度组8/8,20摄氏度组9/10),但48小时冷藏胰腺的胰岛在20摄氏度下消化后的成功率显著高于37摄氏度下消化的成功率(37摄氏度组1/8,20摄氏度组7/8,P < 0.05)。我们得出结论,采用低温胶原酶消化法可从48小时冷藏的胰腺中分离出有活力的胰岛,这显示出有望成为成功进行临床胰岛移植的一种方法。

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