Lassoued K, Nuñez C A, Billips L, Kubagawa H, Monteiro R C, LeBlen T W, Cooper M D
Department of Medicine, University of Alabama, Birmingham 35294.
Cell. 1993 Apr 9;73(1):73-86. doi: 10.1016/0092-8674(93)90161-i.
Surrogate light chain (psi LC) genes are transcriptionally active in progenitor B (pro-B) cells before immunoglobulin genes are rearranged. Current hypothetical models suggest that the psi LC proteins may couple with surrogate or conventional heavy chain proteins to form cell surface receptors that signal the progressive differentiation of pro-B, precursor B (pre-B), and immature B cells. Monoclonal antibodies were produced and used to examine the synthesis, expression, intermolecular interaction, and function of psi LC during B cell differentiation. The results indicate that, while psi LC production spans several developmental stages, cell surface expression is confined to a relatively late stage in normal pre-B cell differentiation, during which receptor cross-linkage does not impede cell growth or B cell differentiation.
替代轻链(ψLC)基因在免疫球蛋白基因重排之前在祖B(pro-B)细胞中具有转录活性。当前的假设模型表明,ψLC蛋白可能与替代或常规重链蛋白结合,形成细胞表面受体,这些受体发出信号促进pro-B、前体B(pre-B)和未成熟B细胞的逐步分化。制备了单克隆抗体并用于检测B细胞分化过程中ψLC的合成、表达、分子间相互作用和功能。结果表明,虽然ψLC的产生跨越多个发育阶段,但细胞表面表达仅限于正常pre-B细胞分化的相对晚期,在此期间受体交联不会阻碍细胞生长或B细胞分化。