King L B, Corley R B
Department of Microbiology and Immunology, Duke University Medical Center, Durham, NC 27710.
Proc Natl Acad Sci U S A. 1989 Apr;86(8):2814-8. doi: 10.1073/pnas.86.8.2814.
We have identified and characterized an inducible in vitro subclone of the CH12 B-cell lymphoma, CH12-LBK, which appears to represent a transitional phase in the B-cell differentiation pathway. This phase, which we call the "presecretory" phase, falls between replicating B cells that are not secreting antibodies and B cells that secrete antibody at a high rate. Presecretory cells are characterized by abundant steady-state levels of immunoglobulin and joining (J) chain transcripts and of protein but low levels of mouse mammary tumor virus envelope transcripts and low rates of immunoglobulin secretion. Additional stimulation is required for presecretory cells to differentiate into cells that secrete antibodies at a high rate. The existence of cells with this phenotype suggests that high-level expression of immunoglobulin and J-chain protein does not necessarily commit a B cell to polymerize and secrete multimeric immunoglobulin. Rather, other gene products, expressed after immunoglobulin and J-chain transcripts have been upregulated late in B-cell differentiation, appear responsible for inducing high rates of antibody secretion.
我们已经鉴定并表征了CH12 B细胞淋巴瘤的一种可诱导的体外亚克隆CH12-LBK,它似乎代表了B细胞分化途径中的一个过渡阶段。这个阶段,我们称之为“分泌前”阶段,介于不分泌抗体的增殖B细胞和高速分泌抗体的B细胞之间。分泌前细胞的特征是免疫球蛋白和连接(J)链转录本以及蛋白质的稳态水平丰富,但小鼠乳腺肿瘤病毒包膜转录本水平低,免疫球蛋白分泌率也低。分泌前细胞需要额外的刺激才能分化成高速分泌抗体的细胞。具有这种表型的细胞的存在表明,免疫球蛋白和J链蛋白的高水平表达不一定会使B细胞聚合并分泌多聚体免疫球蛋白。相反,在B细胞分化后期免疫球蛋白和J链转录本上调后表达的其他基因产物,似乎负责诱导高抗体分泌率。