Wohlrab F, Schmidt S, Kloeting I, Wilke B, Cossel L
Institut für Pathologische Anatomie des Bereiches Medizin, Karl-Max-Universität, Leipzig.
Acta Histochem Suppl. 1990;39:291-5.
Syngeneic transplantation of cultured and functionally characterized neonatal islet into the spleen of streptozotocin diabetic Lewis rats resulted in long time survival up to 200 days and in plasma glucose levels lower than 9 mmol/l. The daily plasma glucose profile of transplanted rats had shown significantly above that of non diabetic control rats. 200 days after transplantation morphologically intact, insulin containing beta-cells were demonstrable in the spleen, thus demonstrating the long-term survival of functioning islet cells. Proliferation of beta-cells was shown in the transplanted islets. In addition, beta-cell clusters were found which derived from pancreatic ductules transplanted together with the isolated islets into the spleen. Mitose were visible within ductular epithelial cells. The proliferative response of islets after intrasplenic transplantation is probably the result of a long-term stimulation by slightly enhanced plasma glucose values of the transplanted acceptors compared to control animals.
将培养并经功能鉴定的新生胰岛同基因移植到链脲佐菌素诱导的糖尿病Lewis大鼠脾脏中,可使大鼠存活长达200天,且血浆葡萄糖水平低于9 mmol/L。移植大鼠的每日血浆葡萄糖曲线显著高于非糖尿病对照大鼠。移植后200天,在脾脏中可检测到形态完整、含胰岛素的β细胞,从而证明了有功能的胰岛细胞能长期存活。移植的胰岛中显示出β细胞增殖。此外,还发现了β细胞簇,其源自与分离的胰岛一起移植到脾脏中的胰腺小导管。在小导管上皮细胞内可见有丝分裂。与对照动物相比,脾内移植后胰岛的增殖反应可能是由于移植受体的血浆葡萄糖值略有升高而长期刺激所致。