Sonenshein G E, Siekevitz M, Siebert G R, Gefter M L
J Exp Med. 1978 Jul 1;148(1):301-12. doi: 10.1084/jem.148.1.301.
Cells of the 315LV-1 (derived from NP1) variant line of MOPC 315 contain approximately 1% the normal intracellular level of the heavy (alpha) chain of IgA and no detectable light (lambda2) chain. The synthesis rate of alpha-chain in the variant, however, is similar to that in cells of the parent line. Moreover the relative amount of translatable alpha-chain mRNA that can be extracted from 315LV-1 cells is about the same as for parental cells. No light-chain synthesis can be detected either in vivo or in vitro in a wheat germ cell-free system. The 315LV-1 heavy chain synthesized in vivo or in vitro has slightly greater electrophoretic mobility than normal H chain and turns over rapidly intracellularly. The variant fails to secrete any of its heavy chain, despite the fact that its H chain mRNA is bound to membranes, as one would expect for a secretory protein message. Fusion of 315LV-1 cells with cells of a kappa-producing MPC 11 variant line leads to stabilization of the intracellular H chain and also to full recovery of secretion of the H chain as an H2L2 molecule.
MOPC 315的315LV - 1(源自NP1)变异株细胞内IgA重链(α链)的含量约为正常细胞内水平的1%,且未检测到轻链(λ2链)。然而,该变异株中α链的合成速率与亲代细胞中的相似。此外,从315LV - 1细胞中提取的可翻译α链mRNA的相对量与亲代细胞大致相同。在小麦胚芽无细胞系统中,无论是体内还是体外均未检测到轻链合成。在体内或体外合成的315LV - 1重链的电泳迁移率略高于正常重链,且在细胞内周转迅速。尽管其H链mRNA如分泌蛋白信息那样与膜结合,但该变异株仍无法分泌任何重链。将315LV - 1细胞与产生κ链的MPC 11变异株细胞融合,可使细胞内H链稳定,并且H链作为H2L2分子的分泌也能完全恢复。