Diabetes Research Institute, Miller School of Medicine, University of Miami, FL, USA.
Department of Surgery, Division of Cellular Transplantation, cGMP Advanced Cell and Biologic Manufacturing Facility, Miller School of Medicine, University of Miami, FL, USA.
Cell Transplant. 2020 Jan-Dec;29:963689720908278. doi: 10.1177/0963689720908278.
Standardized islet characterization assays that can provide results in a timely manner are essential for successful islet cell transplantation. A critical component of islet cell quality is β-cell function, and perifusion-based assessments of dynamic glucose-stimulated insulin secretion (GSIS) are the most informative method to assess this, as they provide the most complex in vitro evaluation of GSIS. However, protocols used vary considerably among centers and investigators as they often use different low- and high-glucose concentrations, exposure-times, flow-rates, oxygen concentrations, islet numbers, analytical methods, measurement units, and instruments, which result in different readouts and make comparisons across platforms difficult. Additionally, the conditions of islet storage and shipment prior to assessment may also affect islet function. Establishing improved standardized protocols for perifusion GSIS assays should be an integral part of the ongoing effort to increase the rigor of human islet studies. Here, we performed detailed evaluation of GSIS of human islets using a fully automated multichannel perifusion instrument following various warm-up recovery times after cold storage that corresponds to current shipping conditions (8°C). We found that recovery times shorter than 18 h (overnight) resulted in impaired insulin secretion. While the effects were relatively moderate on second-phase insulin secretion, first-phase peaks were restored only following 18-h incubation. Hence, the biphasic profile of dynamic GSIS was considerably affected when islets were not allowed to recover for a sufficient time after being maintained in cold. Accordingly, while cold storage might improve islet cell survival during shipment and prolong the length of culture, functional assessments should be performed only after allowing for at least overnight recovery at physiological temperatures.
标准化的胰岛功能检测方法可以及时提供结果,对于成功进行胰岛细胞移植至关重要。胰岛细胞质量的一个关键组成部分是β细胞功能,基于灌流的动态葡萄糖刺激胰岛素分泌(GSIS)评估是评估β细胞功能的最具信息量的方法,因为它提供了对 GSIS 的最复杂的体外评估。然而,由于不同中心和研究人员经常使用不同的低糖和高糖浓度、暴露时间、流速、氧浓度、胰岛数量、分析方法、测量单位和仪器,因此胰岛细胞质量的评估方法差异很大,这导致了不同的读数,并使得跨平台的比较变得困难。此外,在评估之前胰岛的储存和运输条件也可能影响胰岛的功能。建立改进的胰岛灌流 GSIS 检测标准化方案应是提高人类胰岛研究严谨性的重要组成部分。在这里,我们使用全自动多通道灌流仪器对冷藏后不同预热恢复时间(对应当前运输条件 8°C)下的人胰岛 GSIS 进行了详细评估。我们发现,恢复时间短于 18 小时(过夜)会导致胰岛素分泌受损。虽然对第二时相胰岛素分泌的影响相对适中,但只有在 18 小时孵育后才能恢复第一时相峰值。因此,当胰岛在冷藏后没有足够的时间恢复时,动态 GSIS 的双相谱会受到相当大的影响。因此,虽然冷藏可以提高运输过程中胰岛细胞的存活率并延长培养时间,但只有在允许至少过夜恢复到生理温度后,才能进行功能评估。