Steiniger B, Hiller W F, Klempnauer J
Center of Anatomy, Hanover Medical School, West Germany.
Am J Pathol. 1990 Jul;137(1):93-102.
The course of acute rejection of major histocompatibility complex (MHC)-incompatible isolated rat pancreatic islets transplanted under the kidney capsule was monitored functionally and histologically from day 1 to 10. The patterns observed were compared to those of vascularized whole-pancreas transplants with preserved and suppressed exocrine secretion. In addition the morphologic reactions after isogenic transplantation of islets or whole-pancreas transplants are described. The sequential patterns of acute rejection were found to be essentially identical in isolated islet and whole-pancreas allografts. This was also true for the process of I-A-like class II MHC antigen induction. Endocrine cell necrosis and reduced insulin content of beta cells were detected in isolated islets but not in whole-organ isografts. Thus ischemic damage may have occurred to be transplanted islets on days 1 and 2 because connections to the renal vasculature were not demonstrated before day 3. Islet cell loss was, however, functionally compensated by beta cell proliferation beginning on day 4. From the first day after transplantation, an altered spacial distribution of insulin- and glucagon-containing cells was present in islet isografts. This phenomenon was, however, not unique to islets, but also occurred in duct-ligated whole-organ isografts on days 6 to 10.
从第1天至第10天,对在肾被膜下移植的主要组织相容性复合体(MHC)不相容的离体大鼠胰岛急性排斥反应的过程进行了功能和组织学监测。将观察到的模式与保留和抑制外分泌的血管化全胰腺移植的模式进行比较。此外,还描述了胰岛或全胰腺移植的同基因移植后的形态学反应。发现离体胰岛和全胰腺同种异体移植中急性排斥反应的顺序模式基本相同。I-A样II类MHC抗原诱导过程也是如此。在离体胰岛中检测到内分泌细胞坏死和β细胞胰岛素含量降低,但在全器官同基因移植中未检测到。因此,在第1天和第2天,移植的胰岛可能发生了缺血损伤,因为在第3天之前未显示与肾血管系统的连接。然而,从第4天开始,胰岛细胞损失通过β细胞增殖在功能上得到了补偿。从移植后的第一天起,胰岛同基因移植中就出现了含胰岛素和胰高血糖素细胞的空间分布改变。然而,这种现象并非胰岛所特有,在第6至10天的导管结扎全器官同基因移植中也会出现。