Kiessling R, Petranyi G, Klein G, Wigzel H
Int J Cancer. 1975 Jun 15;15(6):933-40. doi: 10.1002/ijc.2910150608.
Spleens of normal young mice of certain genotypes contain lymphocytes that can kill strain A-derived YAC-1 and some other in vitro-grown Moloney lymphoma lines in a 51Cr-release cytotoxic test. We have previously shown that mouse strains can be classified as high or low reactors in this test. F(1) hybrids between low- and high-reactive strains are high-reactive. In the present study, strain-A mice and eight different A F(1) hybrids were tested in parallel for their spleen-cell-mediated killing effect in vitro and their ability to reject graded numbers of YAC ascites or in vitro cultivated cells in vivo. There was a clear correlation between in vitro cytotoxicity and in vivo rejection in all tested genotypes. In segregating (A times C57Bl) times A backcross mice, in vivo rejection of YAC cells was H-2 linked. This is in line with the earlier backcross analysis of the in vitro cytotoxicity, suggesting a polygenic control with at least one H-2 linked factor.
某些基因型的正常幼鼠脾脏中含有淋巴细胞,在51Cr释放细胞毒性试验中,这些淋巴细胞能够杀死A品系来源的YAC - 1细胞以及其他一些体外培养的莫洛尼淋巴瘤细胞系。我们之前已经表明,在该试验中,小鼠品系可分为高反应型或低反应型。低反应型和高反应型品系之间的F(1)杂种是高反应型。在本研究中,同时测试了A品系小鼠和8种不同的A F(1)杂种的脾细胞介导的体外杀伤作用,以及它们在体内排斥不同数量YAC腹水或体外培养细胞的能力。在所有测试的基因型中,体外细胞毒性和体内排斥之间存在明显的相关性。在(A×C57Bl)×A回交小鼠中,YAC细胞的体内排斥与H - 2连锁。这与早期对体外细胞毒性的回交分析一致,表明存在多基因控制,其中至少有一个与H - 2连锁的因子。