Miyamoto M, Inoue K, Gu Y, Tun T, Cui W, Fujiwara I, Ohyanagi H, Hayashi H, Yamazaki T, Setoyama H, Kawakami Y, Ida J, Kogire M, Imamura M, Iwata H, Ikada Y
Department of Surgery II, Kinki University School of Medicine, Osakasayama-City, Osaka, Japan.
Cell Transplant. 1998 Jul-Aug;7(4):397-402. doi: 10.1177/096368979800700408.
To establish a large-scale isolation procedure for adult porcine islets usable as a donor source for xenotransplantation and as a model of human islet isolation, we improved several characteristics of the conventional isolation procedure. At a slaughterhouse we first selected a breeder pig over 1.5 years old (and over 200 kg in weight) with warm ischemic time (WIT) of 15 +/- 2 minutes as nonheart-beating donors. Then, we made a special enzymic mixture that consisted of collagenase S-1 (260 U/mg, NittaZelatin, Japan), collagenase P (1.86 U/ml Lyo Boehringer-Mannheim, USA), DNase (Sigma, St. Louis, Mo), Disparse (NittaZelatin, Japan), and protease inhibitor (Sigma). Third, this mixture was injected very gently into the pancreatic duct at the time of pancreatic harvesting. To prevent overdigestion of the pancreas, the mixture was first cooled to less than 10 degrees C. Fourth, during the warm digestion of pancreas, the pancreas with the enzymic mixture was quietly put in a water bath at 37 degrees C without mechanical shaking. Fifth, we purified the islets with a COBE 2991 cell processor by the Dextran 70 gradient method, because Dextran 70 is very cheap and has the same purification effect as the Ficoll gradient. The results of 10 consecutive breeder porcine islet isolations are reported. The total yield of isolations of islets over 50 microm in the longest diameter after staining with Dithizone (DTZ) was 85,900 +/- 19,954 islets, 291,667 +/- 240,452 IEQ (2,900 +/- 2,324 IEQ/g). The purity of the isolated islets was very high: 90.2 +/- 3.8%. Glucose stimulation during in vitro incubation induced significant insulin release from isolated breeder porcine islets. In two of the diabetic rats receiving encapsulated islets grafts using a mesh-reinforced polyvinyl alcohol hydrogel bag (MRPB), a prominent reduction in serum glucose levels (less than 200 mg/dL) persisted for 13 and 19 days, respectively, after intraperitoneal xenotransplantation islets without immunosuppression. In conclusion, we succeeded in a more efficient and less-expensive isolation of a large amount of adult porcine islets from a nonheart-beating donor.
为建立一种大规模分离成年猪胰岛的方法,该方法可将成年猪胰岛用作异种移植的供体来源,并作为人胰岛分离的模型,我们对传统分离方法的几个特性进行了改进。在一家屠宰场,我们首先选择年龄超过1.5岁(体重超过200千克)、热缺血时间(WIT)为15±2分钟的种猪作为非心跳供体。然后,我们制备了一种特殊的酶混合物,其成分包括胶原酶S-1(260 U/mg,日本日东纺织株式会社)、胶原酶P(1.86 U/ml,美国勃林格殷格翰公司)、脱氧核糖核酸酶(Sigma公司,密苏里州圣路易斯)、分散酶(日本日东纺织株式会社)和蛋白酶抑制剂(Sigma公司)。第三,在摘取胰腺时,将这种混合物非常轻柔地注入胰管。为防止胰腺过度消化,先将混合物冷却至低于10摄氏度。第四,在胰腺的温育消化过程中,将含有酶混合物的胰腺轻轻放入37摄氏度的水浴中,不进行机械振荡。第五,我们使用COBE 2991细胞处理器通过葡聚糖70梯度法纯化胰岛,因为葡聚糖70非常便宜,且具有与菲可梯度相同的纯化效果。报告了连续10次种猪胰岛分离的结果。用双硫腙(DTZ)染色后,最长直径超过50微米的胰岛分离总产量为85,900±19,954个胰岛,291,667±240,452胰岛当量(2,900±2,324胰岛当量/克)。分离出的胰岛纯度非常高:90.2±3.8%。体外孵育期间的葡萄糖刺激诱导分离出的种猪胰岛显著释放胰岛素。在两只接受使用网状增强聚乙烯醇水凝胶袋(MRPB)封装胰岛移植的糖尿病大鼠中,腹腔内异种移植胰岛且未进行免疫抑制后,血清葡萄糖水平显著降低(低于200毫克/分升)分别持续了13天和19天。总之,我们成功地从非心跳供体中更高效、低成本地分离出了大量成年猪胰岛。