Xu B, Iwata H, Miyamoto M, Balamurugan A N, Murakami Y, Cui W, Imamura M, Inoue K
First Department of Surgery and Surgical Basic Science, Graduate School of Medicine, Kyoto University, Japan.
Cell Transplant. 2001;10(4-5):403-8.
In this study, the insulin secretory characteristics of the microencapsulated hamster islets were studied during long-term culture. The hamster islets were encapsulated as single-layer agarose microbeads or three-layer agarose microbeads with agarose and agarose containing poly(styrene sulfonic acid) (PSSa), respectively. The influence of PSSa on the function of the rat islets microencapsulted in three-layer microbeads was primarily monitored. The aim of this study was to examine the influence of the PSSa on the in vitro function of the islets encapsulated in the agarose/PSSa microbeads compared with single-layer agarose microbeads during long-term culture. The microbeads were cultured for 30 days in medium of Eagle's MEM at 37 degrees C in 5% CO2 and 95% air. The basal insulin secretion into the culture medium was measured daily during the first 12 days and two times per week until 30 days. The microbeads were subjected to static incubation test on the 10th, 20th, and 30th day during culture. The basal insulin secretion level of the agarose/PSSa microbeads was significantly higher than that of single-layer agarose microbeads. The static incubation tests revealed a similar pattern of insulin secretion from both microbeads when they were exposed to high glucose challenge. In the static incubation test, both could significantly increase insulin release to more than 6.61 times (stimulation index) in response to high glucose stimulation and could significantly decrease when glucose concentration returned from high glucose to low glucose on the 10th, 20th, and 30th day of culture. This study demonstrated that the hamster islets enclosed in agarose/PSSa hydrogel not only continuously secreted basal amounts of insulin, but also maintained their response to high glucose stimulation similar to the agarose microbeads. The above results together with those of our previous in vivo study suggest that the three-layer microbeads (agarose/PSSa) are well suitable for xenotransplantation of islets for the clinical application.
在本研究中,对长期培养过程中微囊化仓鼠胰岛的胰岛素分泌特性进行了研究。仓鼠胰岛分别被封装为单层琼脂糖微珠或由琼脂糖以及含聚苯乙烯磺酸(PSSa)的琼脂糖组成的三层琼脂糖微珠。主要监测了PSSa对封装在三层微珠中的大鼠胰岛功能的影响。本研究的目的是在长期培养过程中,考察与单层琼脂糖微珠相比,PSSa对封装在琼脂糖/PSSa微珠中的胰岛体外功能的影响。将微珠在含5%二氧化碳和95%空气的条件下,于37℃的伊格尔氏MEM培养基中培养30天。在培养的前12天每天测定培养基中基础胰岛素分泌量,直至30天每周测定两次。在培养的第10天、第20天和第30天对微珠进行静态孵育试验。琼脂糖/PSSa微珠的基础胰岛素分泌水平显著高于单层琼脂糖微珠。静态孵育试验显示,当两种微珠受到高糖刺激时,胰岛素分泌模式相似。在静态孵育试验中,在培养的第10天、第20天和第30天,二者在高糖刺激下均可显著增加胰岛素释放至超过6.61倍(刺激指数),且当葡萄糖浓度从高糖恢复到低糖时均可显著降低。本研究表明,封装在琼脂糖/PSSa水凝胶中的仓鼠胰岛不仅持续分泌基础量的胰岛素,而且维持了与琼脂糖微珠相似的对高糖刺激的反应。上述结果与我们之前的体内研究结果共同表明,三层微珠(琼脂糖/PSSa)非常适合胰岛的异种移植用于临床应用。