Nakayama-Iwatsuki Kenyu, Hirabayashi Masumi, Hochi Shinichi
Graduate School of Medicine, Science and Technology, Shinshu University, Ueda, Nagano, Japan.
National Institute for Physiological Sciences, Okazaki, Aichi, Japan.
J Tissue Eng Regen Med. 2021 Jul;15(7):686-696. doi: 10.1002/term.3219. Epub 2021 May 22.
Dispersed single cells from pancreatic islets can configure the three-dimensional islet-like architecture (pseudo-islets) with insulin secretion potential and controllable size through their aggregation property. The present study was designed to investigate whether cryopreservation of islets or islet cells can contribute to the efficient pseudo-islet fabrication in the rat model. In control group (CT), islet single cells were prepared by trypsin digestion of 50-400-µm ø fresh control islets, and then cultured for 3 days in the U-bottom microwell to fabricate pseudo-islets. In vitrification-warming group (VW), islet single cells were prepared from postwarm islets cryopreserved by vitrification on nylon mesh device, and then cultured for 3 days. In freezing group (FR), islet single cells originated from fresh islets were subjected to a conventional Bicell freezing, and postthaw cells were cultured for 3 days. To generate 1 islet equivalent pseudo-islets (150 µm ø) by the sphere culture, 1250 CT cells, 1250 VW cells, and 1500 FR cells were seeded to each microwell. The viability of the pseudo-islets was comparable among the three groups (93.9%-96.9%). Furthermore, the insulin secretion assay showed that those pseudo-islets responded sufficiently to the high glucose stimulation. Immunostaining for insulin and glucagon showed that the endocrine cell arrangement of those pseudo-islets is similar to that of native and isolated islets. These islets/pseudo-islets had the β-cells in core and the α-cells in mantle, which was typical characteristic of the rodent islets. However, some clusters of α-cells were observed inside the FR pseudo-islets. Interestingly, the VW pseudo-islets had significantly fewer α-cells than the CT or FR pseudo-islets. These results suggest that the sphere culture of islet cells is useful tool to generate the pseudo-islets with the customized size and normal functionality, even after islet cryopreservation.
来自胰岛的分散单细胞可通过其聚集特性构建具有胰岛素分泌潜力且大小可控的三维胰岛样结构(伪胰岛)。本研究旨在探讨胰岛或胰岛细胞的冷冻保存是否有助于在大鼠模型中高效制备伪胰岛。在对照组(CT)中,通过胰蛋白酶消化50 - 400 µm ø 的新鲜对照胰岛制备胰岛单细胞,然后在U型底微孔板中培养3天以制备伪胰岛。在玻璃化复温组(VW)中,胰岛单细胞由在尼龙网装置上经玻璃化冷冻保存后复温的胰岛制备,然后培养3天。在冷冻组(FR)中,将来自新鲜胰岛的胰岛单细胞进行常规双细胞冷冻,解冻后的细胞培养3天。为通过球体培养生成1个胰岛当量的伪胰岛(150 µm ø),向每个微孔板接种1250个CT细胞、1250个VW细胞和1500个FR细胞。三组伪胰岛的活力相当(93.9% - 96.9%)。此外,胰岛素分泌测定表明,这些伪胰岛对高糖刺激有充分反应。胰岛素和胰高血糖素免疫染色显示,这些伪胰岛的内分泌细胞排列与天然和分离的胰岛相似。这些胰岛/伪胰岛的核心为β细胞,外层为α细胞,这是啮齿动物胰岛的典型特征。然而,在FR伪胰岛内部观察到一些α细胞簇。有趣的是,VW伪胰岛中的α细胞明显少于CT或FR伪胰岛。这些结果表明,即使在胰岛冷冻保存后,胰岛细胞的球体培养也是生成具有定制大小和正常功能的伪胰岛的有用工具。