Weeks R S, Sibley C H
Department of Genetics, University of Washington, Seattle 98195.
J Immunol. 1988 Feb 15;140(4):1312-20.
The murine B cell lymphoma, 70Z/3, serves as a model for the L chain activation seen when normal B cells develop from pre-B into B cells. 70Z/3 cells can be induced to activate transcription of their endogenous kappa L chain by exposure to exogenous factors in vitro, such as LPS and IFN-gamma. In order to study the interaction of transacting factors with sequences of the kappa gene responsible for their activation, altered kappa genes could be introduced into 70Z/3 cells and their induction patterns studied. As a preliminary step to such studies, we show that wild-type kappa genes stably integrated into 70Z/3 cells can be expressed normally and that their pattern of induction by LPS and IFN-gamma is indistinguishable from wild-type 70Z/3 cells. By using electroporation, gamma genes were co-transfected with either the neo or gpt selectable genes. In all cases, the expression of the kappa genes was autonomous, reflecting neither regulation by the selected markers nor by flanking chromosome sequences. A noninducible variant of 70Z/3, NN12, also increased mRNA levels from transfected kappa genes in response to LPS and IFN-gamma, suggesting that its defect is in its endogenous kappa gene. These results demonstrated the usefulness of this approach for distinguishing between variants that have structural defects in their endogenous kappa gene from variants that have defects in transacting factors or other steps in the induction pathways.
小鼠B细胞淋巴瘤70Z/3可作为正常B细胞从前B细胞发育为B细胞时所见轻链激活的模型。70Z/3细胞在体外暴露于外源性因子(如脂多糖和干扰素-γ)时,可被诱导激活其内源性κ轻链的转录。为了研究反式作用因子与负责激活的κ基因序列之间的相互作用,可将改变的κ基因导入70Z/3细胞并研究其诱导模式。作为此类研究的初步步骤,我们发现稳定整合到70Z/3细胞中的野生型κ基因能够正常表达,并且它们受脂多糖和干扰素-γ诱导的模式与野生型70Z/3细胞没有区别。通过电穿孔法,将κ基因与新霉素或黄嘌呤-鸟嘌呤磷酸核糖转移酶选择基因共转染。在所有情况下,κ基因的表达都是自主的,既不反映所选标记的调控,也不反映侧翼染色体序列的调控。70Z/3的一种非诱导型变体NN12,在脂多糖和干扰素-γ作用下,也会使转染的κ基因的mRNA水平升高,这表明其缺陷在于其内源性κ基因。这些结果证明了这种方法对于区分内源性κ基因存在结构缺陷的变体与反式作用因子或诱导途径中其他步骤存在缺陷的变体的有用性。