Brandhorst D, Iken M, Brendel M D, Bretzel R G, Brandhorst H
Third Medical Department, University Hospital, Giessen, Germany.
Transplant Proc. 2005 Jan-Feb;37(1):458-9. doi: 10.1016/j.transproceed.2004.12.035.
Islet release from the pancreas is mediated by both collagenase and neutral protease (NP), a critical effector of islet integrity. To prove the hypothesis that adjustment of NP reduces islet damage after prolonged ischemia, adult pig pancreata were digested after 7-hour preservation by the two-layer method (TLM) using a 2-component enzyme blend consisting of collagenase NB-8 and NP.
After intraductal University of Wisconsin (UW) flush resected pancreata were distended with 4.4 PZ-U/g of UW-dissolved Serva collagenase either before (TLM-preloaded, n = 7) or after (TLM-postloaded, n = 10) cold storage, or for immediate processing (n = 6). NP was adjusted after preliminary experiments to respectively 1.1, 0.2, or 0.8 DMC-U/g for unstored, TLM-preloaded, or postloaded organs.
Purified islet yield decreased from 3670 +/- 730 islet equivalents (IEQ)/g in unstored pancreata to 1800 +/- 180 and 2080 +/- 290 IEQ/g in TLM-preloaded or postloaded organs, respectively (P < .05). Although purity was always >90%, IEQ recovery was significantly decreased in TLM-preloaded pancreata. Quality control revealed consistently high viability as determined using trypan-blue exclusion (>95%) or formazan production. Compared with unstored organs (2.47 +/- 0.36; P < .05), glucose stimulation index was reduced in TLM-preloaded (1.48 +/- 0.15) and TLM-postloaded pancreata (1.81 +/- 0.20). Normoglycemia in diabetic nude mice transplanted with islets from TLM-preloaded pancreata was transient in contrast to sustained function in the other groups.
Significant amounts of viable pig islets can be isolated after prolonged TLM preservation by reducing NP activity. Nevertheless, early enzyme administration prior to long-term storage deteriorates islet graft function.
胰岛从胰腺中释放由胶原酶和中性蛋白酶(NP)介导,NP是胰岛完整性的关键效应因子。为了验证调整NP可减少长时间缺血后胰岛损伤这一假说,采用由胶原酶NB - 8和NP组成的双组分酶混合物,通过两层法(TLM)对成年猪胰腺进行7小时保存后进行消化。
经导管灌注威斯康星大学(UW)液后,切除的胰腺在冷藏前(TLM预加载组,n = 7)或冷藏后(TLM后加载组,n = 10),用4.4 PZ - U/g的UW溶解的Serva胶原酶充盈,或立即进行处理(n = 6)。经过初步实验后,将未储存、TLM预加载或后加载器官的NP分别调整为1.1、0.2或0.8 DMC - U/g。
纯化的胰岛产量从未储存胰腺的3670±730胰岛当量(IEQ)/g分别降至TLM预加载或后加载器官的1800±180和2080±290 IEQ/g(P <.05)。尽管纯度始终>90%,但TLM预加载胰腺的IEQ回收率显著降低。质量控制显示,使用台盼蓝排斥法(>95%)或甲臜生成法测定,活力始终很高。与未储存器官(2.47±0.36;P <.05)相比,TLM预加载(1.48±0.15)和TLM后加载胰腺(1.81±0.20)的葡萄糖刺激指数降低。移植来自TLM预加载胰腺的胰岛的糖尿病裸鼠的正常血糖是短暂的,而其他组则具有持续功能。
通过降低NP活性,长时间TLM保存后可分离出大量有活力的猪胰岛。然而,长期储存前早期给予酶会使胰岛移植功能恶化。