Kasahara Naoya, Teratani Takumi, Doi Junshi, Iijima Yuki, Maeda Masashi, Uemoto Shinji, Fujimoto Yasuhiro, Sata Naohiro, Yasuda Yoshikazu, Kobayashi Eiji
Division of Development of Advanced Therapy, Center for Development of Advanced Medical Technology, Jichi Medical University, Shimotsukeshi, Tochigi, Japan; †Department of Surgery, Jichi Medical University, Shimotsukeshi, Tochigi, Japan.
Division of Development of Advanced Therapy, Center for Development of Advanced Medical Technology, Jichi Medical University , Shimotsukeshi, Tochigi , Japan.
Cell Med. 2013 May 14;5(2-3):75-81. doi: 10.3727/215517913X666477. eCollection 2013 Nov 10.
Pancreatic islet transplantation has received widespread attention as a promising treatment for type 1 diabetes. However, islets for transplantation are subject to damage from a number of sources, including ischemic injury during removal and delivery of the donor pancreas, enzymatic digestion during islet isolation, and reperfusion injury after transplantation in the recipient. Here we found that protein fractions secreted by mesenchymal stem cells (MSCs) were capable of activating preserved islets. A conditioned medium from the supernatant obtained by culturing adipose tissue MSCs (derived from wild-type Lewis rats) was prepared for 2 days in serum-free medium. Luc-Tg rat islets to which an organ preservation solution was added were then incubated at 4°C with fractions of various molecular weights prepared from the conditioned medium. Under the treatment with some of the fractions, by 4 days the relative luminescence intensities (representative of the ATP levels of the cold-preserved islets) had increased to over 150% of their initial values. Our novel system may be able to restore isolated islets to the condition they were in before transport, culture, and transplantation.
胰岛移植作为1型糖尿病一种有前景的治疗方法已受到广泛关注。然而,用于移植的胰岛会受到多种来源的损伤,包括供体胰腺切除和递送过程中的缺血损伤、胰岛分离过程中的酶消化以及受体移植后的再灌注损伤。在此,我们发现间充质干细胞(MSC)分泌的蛋白质组分能够激活保存的胰岛。将来自野生型Lewis大鼠的脂肪组织MSC在无血清培养基中培养2天,制备其上清液的条件培养基。然后将添加了器官保存溶液的Luc-Tg大鼠胰岛在4°C下与从条件培养基中制备的各种分子量的组分一起孵育。在用某些组分处理后,到第4天,相对发光强度(代表冷保存胰岛的ATP水平)增加到其初始值的150%以上。我们的新系统或许能够将分离的胰岛恢复到运输、培养和移植前的状态。