Tsubata T, Reth M
Max-Planck Institute for Immunobiology, Freiburg, Federal Republic of Germany.
J Exp Med. 1990 Sep 1;172(3):973-6. doi: 10.1084/jem.172.3.973.
We constructed expression vectors coding for the two pre-B-specific genes, VpreB and lambda 5, and transfected them together with a mu vector (mu tm) into Ig- myeloma cells. In a transfectant expressing all three introduced genes, the mu tm chain is transported on the cell surface. A biochemical analysis demonstrated that, in these cells, the mu tm chain is associated noncovalently with an 18-kD protein and covalently with a 22-kD protein, which are most likely the products of VpreB and lambda 5, respectively. Our results, thus, strongly suggest that the products of lambda 5 and VpreB bind to mu chains and have the same capacity as conventional Ig L chains to allow surface expression of mu chains.
我们构建了编码两个前B细胞特异性基因VpreB和λ5的表达载体,并将它们与一个μ载体(μtm)一起转染到Ig-骨髓瘤细胞中。在一个表达所有三个导入基因的转染子中,μtm链被转运到细胞表面。生化分析表明,在这些细胞中,μtm链与一个18-kD蛋白非共价结合,与一个22-kD蛋白共价结合,这两个蛋白很可能分别是VpreB和λ5的产物。因此,我们的结果强烈表明,λ5和VpreB的产物与μ链结合,并且具有与传统Ig轻链相同的能力,能够使μ链在细胞表面表达。