Matsumoto Shinichi, Qualley Sabrina A, Goel Shilpa, Hagman Derek K, Sweet Ian R, Poitout Vincent, Strong D Michael, Robertson R Paul, Reems Jo Anna
Islet and Cell Processing Laboratory (ICPL) at Puget Sound Blood Center and Northwest Tissue Center, Seattle, WA, USA.
Transplantation. 2002 Nov 27;74(10):1414-9. doi: 10.1097/00007890-200211270-00013.
Current techniques for isolating islets require that pancreata stored with University of Wisconsin solution (UW) are processed within 12 hours of cold storage. In this study, we hypothesized that the two-layer method (TLM) could extend the acceptable preservation period of pancreata before islet isolation and increase islet yields.
In the first experimental set, eight pancreata were maintained for an average of 8.3+/-1.2 hours in UW and transferred into the TLM for an additional 14.3+/-1.1 hours for a total cold ischemic period of 22.6+/-1.6 hours (prolonged TLM). Four pancreata were maintained as a control group in UW alone for a total of 21.3+/-2.0 hours. In the second experimental set, six pancreata were maintained for an average of 6.4+/-1.8 hours in UW followed by 4.8+/-0.8 hours with the TLM for a total preservation time of 11.3+/-2.5 hours (short TLM). The control organs for the short TLM group were stored for an average of 9.5+/-1.3 hours in UW alone. Islets were isolated and evaluated according to the Edmonton protocol.
Between each group of the two experimental sets, there was no significant difference in donor-related factors (i.e. gender, age, body mass index [BMI], etc.). The TLM as compared with UW preservation resulted in a significant increase in islet yields postpurification for both short (3,353+/-394 islet equivalents [IE] vs. 2,027+/-415 IE; mean+/-SEM) and prolonged (2,404+/-503 IE vs. 514+/-180 IE) periods of storage. Furthermore, islet yields after prolonged storage with the TLM were not significantly different from organs maintained for only a short period with UW (P=0.17). The quality of islets as assessed by size, postculture viability, survival rates, insulin content, and insulin secretion were similar for each of the four groups.
In comparison with UW organ preservation, exposure of pancreata to the TLM result in greater islet yields and extended preservation times.
目前分离胰岛的技术要求保存在威斯康星大学溶液(UW)中的胰腺在冷藏12小时内进行处理。在本研究中,我们假设两层法(TLM)可以延长胰岛分离前胰腺的可接受保存期并提高胰岛产量。
在第一组实验中,8个胰腺在UW中平均保存8.3±1.2小时,然后转移到TLM中再保存14.3±1.1小时,总冷缺血时间为22.6±1.6小时(延长的TLM)。4个胰腺作为对照组仅在UW中保存,总时长为21.3±2.0小时。在第二组实验中,6个胰腺在UW中平均保存6.4±1.8小时,然后用TLM保存4.8±0.8小时,总保存时间为11.3±2.5小时(短TLM)。短TLM组的对照器官仅在UW中平均保存9.5±1.3小时。根据埃德蒙顿方案分离并评估胰岛。
在两组实验的每组之间,供体相关因素(即性别、年龄、体重指数[BMI]等)没有显著差异。与UW保存相比,无论是短时间(3353±394个胰岛当量[IE]对2027±415个IE;平均值±标准误)还是长时间(2404±503个IE对514±180个IE)保存,TLM都导致纯化后胰岛产量显著增加。此外,用TLM长时间保存后的胰岛产量与仅在UW中短时间保存的器官没有显著差异(P = 0.17)。通过大小、培养后活力、存活率、胰岛素含量和胰岛素分泌评估的胰岛质量在四组中相似。
与UW器官保存相比,胰腺暴露于TLM可提高胰岛产量并延长保存时间。