Marchetti P, Finke E H, Gerasimidi-Vazeou A, Falqui L, Scharp D W, Lacy P E
Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Transplantation. 1991 Aug;52(2):209-13. doi: 10.1097/00007890-199108000-00005.
To evaluate the potential of utilizing porcine islet tissue as an alternative to human islet tissue for transplantation, we developed a method for the isolation of large amounts of highly purified porcine islets, and assessed the in vitro and in vivo function of the isolated islets after 1, 4, and 7 days of culture. The pancreatic duct of the splenic lobe was cannulated and distended by injection of Hanks' balanced salt solution containing 1.5 mg/ml collagenase. The pancreas was then processed by a modification of the automated digestion-filtration method developed in this laboratory, and with purification accomplished by Euro-Ficoll gradients (dialyzed Ficoll in Eurocollins solution), consisting of two layers of 1.108 and 1.091 g/cm3 density, topped with a layer of HBSS. The postpurification yield was 5203 +/- 645 (mean +/- SEM) islets per gram of pancreas with a number of islet equivalents (IE) per gram pancreas (islet equivalence: 150-microns-sized islets) of 3551 +/- 305, and a volume of 6.27 +/- 1.7 mm3 islet tissue per gram of pancreas. The islet purity exceeded 90%. Overnight-cultured, perifused porcine islets released 53.1 +/- 8.2 pM insulin/200 IE at 3.3 mM glucose, and 114.9 +/- 25.4 pM insulin/200 IE at 16.7 mM glucose (P less than 0.001 vs. basal output). When theophylline was added, insulin secretion increased to 264.2 +/- 63.2 pM/200 IE (P less than 0.001 vs. basal secretion and P less than 0.005 vs. secretion at 16.7 mM glucose). After 4 days of culture, the islets still responded to secretagogues. The functional integrity of the isolated islets was confirmed by reversal of diabetes in aL3T4 antibody-treated C57B/B6 diabetic mice: normoglycemia was promptly restored by transplanting 1000 overnight- or 7-day-cultured (24 degrees C) islets under the kidney capsule. These results suggest that continued improvements of porcine islet isolation and culture could permit the use of porcine islets in immunoalteration and immunoisolation studies that may lead to eventual human transplantation.
为了评估利用猪胰岛组织替代人胰岛组织进行移植的潜力,我们开发了一种分离大量高度纯化猪胰岛的方法,并在培养1天、4天和7天后评估了分离出的胰岛的体外和体内功能。通过注射含1.5mg/ml胶原酶的汉克斯平衡盐溶液,对脾叶的胰管进行插管并扩张。然后,采用本实验室开发的自动消化-过滤方法的改进方法对胰腺进行处理,并通过Euro-Ficoll梯度(Eurocollins溶液中的透析Ficoll)进行纯化,该梯度由两层密度分别为1.108和1.091g/cm³的溶液组成,顶部覆盖一层HBSS。纯化后的产量为每克胰腺5203±645(平均值±标准误)个胰岛,每克胰腺的胰岛当量(IE)数量(胰岛当量:150微米大小的胰岛)为3551±305,每克胰腺的胰岛组织体积为6.27±1.7mm³。胰岛纯度超过90%。过夜培养的灌注猪胰岛在3.3mM葡萄糖浓度下释放53.1±8.2pM胰岛素/200IE,在16.7mM葡萄糖浓度下释放114.9±25.4pM胰岛素/200IE(与基础分泌相比,P<0.001)。加入茶碱后,胰岛素分泌增加到264.2±63.2pM/200IE(与基础分泌相比,P<0.001;与16.7mM葡萄糖浓度下的分泌相比,P<0.005)。培养4天后,胰岛仍对促分泌剂有反应。通过在aL3T4抗体处理的C57B/B6糖尿病小鼠中逆转糖尿病,证实了分离出的胰岛的功能完整性:通过将1000个过夜培养或7天培养(24℃)的胰岛移植到肾被膜下,血糖迅速恢复正常。这些结果表明,猪胰岛分离和培养技术的持续改进可能允许在免疫改变和免疫隔离研究中使用猪胰岛,这可能最终导致人类移植。