Kiesel U, Kolb H, Freytag G
Clin Exp Immunol. 1981 Feb;43(2):430-3.
Multiple treatment with low doses of streptozotocin induces hyperglycaemia with concomitant lymphocytic infiltrations into pancreatic islets (insulitis) in several mouse strains. The transfer of cellular immune reactions against islet cells by means of spleen cells was tested in two congeneic and five allogeneic strain combinations. Donor mice were treated on 5 consecutive days with 40 mg streptozotocin per kg body weight. Three weeks later, 5 x 10(7) live spleen cells were transferred into thymusless recipient mice. Insulitis which had developed in about 70% of the donors was only transferable from C57B1/6J to congeneic thymusless mice. In a second congeneic and in all allogeneic strain combinations, cellular immune reactions against pancreatic islets could not be transferred. In none of the recipients of spleen cells from diabetic donors was hyperglycaemia observed. As streptozotocin-induced cellular immune reactions against pancreatic islet cells were only transferable in one congeneic and in no allogeneic strain combinations, it is concluded that there is a genetic restriction both on the levels of donor and recipient mice.
低剂量链脲佐菌素多次给药可在多种小鼠品系中诱发高血糖症,并伴有淋巴细胞浸润胰腺胰岛(胰岛炎)。通过脾细胞测试了两种同基因和五种异基因品系组合中针对胰岛细胞的细胞免疫反应的转移情况。供体小鼠连续5天接受每千克体重40毫克链脲佐菌素的治疗。三周后,将5×10⁷个活脾细胞转移到无胸腺受体小鼠体内。约70%的供体中出现的胰岛炎仅能从C57B1/6J转移到同基因无胸腺小鼠体内。在第二种同基因和所有异基因品系组合中,针对胰腺胰岛的细胞免疫反应无法转移。在接受糖尿病供体脾细胞的受体中,均未观察到高血糖症。由于链脲佐菌素诱导的针对胰腺胰岛细胞的细胞免疫反应仅在一种同基因品系组合中可转移,而在任何异基因品系组合中均不可转移,因此得出结论,供体和受体小鼠的水平均存在遗传限制。