Malissen B, Price M P, Goverman J M, McMillan M, White J, Kappler J, Marrack P, Pierres A, Pierres M, Hood L
Cell. 1984 Feb;36(2):319-27. doi: 10.1016/0092-8674(84)90225-3.
We have transferred the mouse Ak alpha and Ak beta genes, which encode the class II I-Ak molecule, into mouse L-cell fibroblasts and hamster B cells. I-Ak molecules are expressed on the surface of both cell types. The L-cell and hamster B-cell I-Ak molecules appear normal by serological analyses and two-dimensional gel electrophoresis. Furthermore, the I-Ak molecules on L cells can act as targets for the allogenic T-cell killing of the transformed L cells. The I-Ak molecules in both mouse fibroblasts and hamster B cells can present certain antigens to T-cell helper hybridomas. Thus only class II molecules are required to convert the nonantigen-presenting cell. Accordingly, it will be possible to dissect the structure-function relationships existing between Ia molecules, foreign antigen, and T-cell receptor molecules by in vitro site-directed mutagenesis and gene transfer.
我们已将编码II类I-Ak分子的小鼠Akα和Akβ基因转入小鼠L细胞成纤维细胞和仓鼠B细胞中。I-Ak分子在这两种细胞类型的表面均有表达。通过血清学分析和二维凝胶电泳,L细胞和仓鼠B细胞上的I-Ak分子看起来是正常的。此外,L细胞上的I-Ak分子可作为转化L细胞异体T细胞杀伤的靶标。小鼠成纤维细胞和仓鼠B细胞中的I-Ak分子均可将某些抗原呈递给T细胞辅助性杂交瘤。因此,只需II类分子就能使非抗原呈递细胞发生转化。相应地,通过体外定点诱变和基因转移,剖析Ia分子、外来抗原和T细胞受体分子之间存在的结构-功能关系将成为可能。