Ochi A, Hozumi N
J Immunol. 1986 Apr 1;136(7):2705-8.
The transducing vector, pSV2-neo, carrying the rearranged immunoglobulin (Ig) heavy (mu) and light (kappa) chain genes specific for the hapten 2,4,6-trinitrophenyl (TNP) was introduced into a pre-B cell line. The transformants expressed the TNP-specific IgM receptor on the surface. Furthermore, the addition of TNP-bovine serum albumin (hapten-carrier conjugate) to the culture media activated the expression of the transferred Ig genes and several endogenous genes such as v-abl and beta-tubulin. However, expression of the beta2-microglobulin gene was not affected. The results presented in this paper show that transfection of cloned Ig genes into B cells is a useful system for establishing monoclonal B cell lines expressing functional Ig receptor molecules with defined hapten specificity.
携带针对半抗原2,4,6-三硝基苯(TNP)的重排免疫球蛋白(Ig)重链(μ)和轻链(κ)基因的转导载体pSV2-neo被导入一个前B细胞系。转化体在表面表达TNP特异性IgM受体。此外,向培养基中添加TNP-牛血清白蛋白(半抗原-载体偶联物)可激活转移的Ig基因以及一些内源性基因如v-abl和β-微管蛋白的表达。然而,β2-微球蛋白基因的表达不受影响。本文给出的结果表明,将克隆的Ig基因转染到B细胞中是建立表达具有明确半抗原特异性的功能性Ig受体分子的单克隆B细胞系的有用系统。