Baylor Research Institute, Dallas, TX, USA.
Islets. 2011 Nov-Dec;3(6):376-80. doi: 10.4161/isl.3.6.18159.
Establishing a prolonged pancreas preservation model in a small animal is important for islet isolation research. Use of a rat pancreas model has been reported, but no published reports have used a mouse pancreas for prolonged cold preservation prior to islet isolation. For the model, a mouse is preferred over a rat because of its small size, well-known immune characterization, and variety of gene-modulated models. In the present study, we established a prolonged pancreas preservation model in a mouse for islet isolation research. The collagenase solution was injected successfully after 24 and 48 h cold preservations in University of Wisconsin solution, and islets could be isolated from both groups of preserved pancreata. The islet yields from the control, 24 h preserved, and 48 h preserved pancreata were 183.9 ± 13.9, 128.5 ± 15.5, and 24.6 ± 12.9 per pancreas, respectively. The propidium iodide-positive area assay was significantly increased in both preserved groups, and insulin secretion levels in response to 20.0 mM glucose and stimulation indices were significantly decreased in the 48 h preserved group. Inflammation-related genes mRNA levels were significantly upregulated in the 24 h preserved group, as previously shown in the human model. Thus, this model might be useful for prehuman islet isolation screening research, reserving research using human pancreata for the most promising approaches.
建立一个可延长的小动物胰腺保存模型对于胰岛分离研究非常重要。已经有报道使用大鼠胰腺模型,但没有使用小鼠胰腺进行胰岛分离前的长时间冷保存的报道。由于小鼠体积小、免疫特征明确,以及具有多种基因修饰模型,因此在该模型中,小鼠比大鼠更受欢迎。在本研究中,我们建立了一种用于胰岛分离研究的可延长小鼠胰腺保存模型。在 UW 溶液中进行 24 和 48 小时冷保存后,胶原酶溶液成功注射,并且可以从两组保存的胰腺中分离出胰岛。对照组、24 小时保存组和 48 小时保存组的胰岛产量分别为 183.9±13.9、128.5±15.5 和 24.6±12.9 个/胰腺。碘化丙啶阳性面积测定在两组保存组中均显著增加,48 小时保存组对 20.0mM 葡萄糖的胰岛素分泌水平和刺激指数显著降低。炎症相关基因 mRNA 水平在 24 小时保存组中显著上调,如前所述在人类模型中。因此,该模型可能有助于人类胰岛分离前的筛选研究,为最有前途的方法保留人类胰腺的研究。