Shearer G M, Polisson R P
J Exp Med. 1980 Jan 1;151(1):20-31. doi: 10.1084/jem.151.1.20.
Four different combinations of F1 hybrid mice [(C57BL/10 X B10.A)F1, (C57BL/10 X B10.BR)F1, B6D2F1, and AKD2F1] were injected intravenously with spleen cells from parental strains. The T-cell-mediated cytotoxic potential of spleen cells from the injected F1 mice was assessed from 4 to 21 d later by in vitro sensitization with trinitrophenyl-modified parental or syngeneic F1 spleen cells (TNP-self) or with allogeneic spleen cells. The cytotoxic potential of the F1 mice to TNP-self as well as to alloantigens was abolished or severely depressed throughout this period when the respective H-2k,a,d parental spleen cells were injected. In contrast, the cytotoxic potential was unaffected or only marginally reduced when H-2b parental cells were injected. The induction of depressed cytotoxic activity was shown to be a result of a population of parental radiosensitive T lymphocytes. The results should be discussed with respect to (a) the genetic and mechanistic parameters associated with the differential depressive effects of parental cells expressing H-2b vs. H-2k,a,d antigens, and (b) the use of this system for investigating allogeneic receptors on T-lymphocyte populations.
将四种不同组合的F1杂交小鼠[(C57BL/10×B10.A)F1、(C57BL/10×B10.BR)F1、B6D2F1和AKD2F1]静脉注射亲本品系的脾细胞。在注射后4至21天,通过用三硝基苯基修饰的亲代或同基因F1脾细胞(TNP-自身)或异基因脾细胞进行体外致敏,评估注射的F1小鼠脾细胞的T细胞介导的细胞毒性潜力。当注射相应的H-2k、a、d亲代脾细胞时,在此期间F1小鼠对TNP-自身以及同种异体抗原的细胞毒性潜力被消除或严重降低。相比之下,当注射H-2b亲代细胞时,细胞毒性潜力未受影响或仅略有降低。已证明细胞毒性活性降低的诱导是亲代放射敏感T淋巴细胞群体的结果。应从以下方面讨论这些结果:(a)与表达H-2b与H-2k、a、d抗原的亲代细胞的差异抑制作用相关的遗传和机制参数,以及(b)使用该系统研究T淋巴细胞群体上的同种异体受体。