Henderson A J, Narayanan R, Collins L, Dorshkind K
Division of Biomedical Sciences, University of California, Riverside 92521-0121.
J Immunol. 1992 Sep 15;149(6):1973-9.
Studies from several laboratories have provided evidence that distinct stromal cell-derived signals are involved in the maturation of pre-B cells into surface Ig expressing B lymphocytes. In order to define the stage of development at which these stimuli act, various polymerase chain reaction strategies were used to characterize the status of kappa L chain gene rearrangements in nontransformed, stromal cell dependent pre-B cells. These cells were obtained from lymphoid colonies whose growth was potentiated by factors from a stromal cell line. kappa L chain genes in cells from many of these colonies were rearranged, and analysis of the Jk genes used indicated a bias toward the most 3' loci. However, the use of a reverse transcriptase PCR strategy failed to detect mature kappa transcripts, indicating that stromal cell mediators exist that allow pre-B cells to progress to the stage at which L chain genes are rearranged but not expressed. Reverse transcriptase PCR further revealed that no transcripts for c-kit (the receptor for kit-ligand) and the IL-7R could be detected in these cells. This suggests that these receptors are no longer expressed by the time cells have undergone kappa rearrangements and minimize a role for stromal cell-derived kit-ligand and IL-7 in mediating the pre-B to B cell transition.
来自多个实验室的研究已提供证据表明,不同的基质细胞衍生信号参与前B细胞成熟为表达表面免疫球蛋白的B淋巴细胞的过程。为了确定这些刺激作用的发育阶段,采用了各种聚合酶链反应策略来表征未转化的、依赖基质细胞的前B细胞中κ轻链基因重排的状态。这些细胞取自淋巴集落,其生长因基质细胞系的因子而增强。许多这些集落的细胞中的κ轻链基因发生了重排,对所使用的Jk基因的分析表明偏向于最3'端的基因座。然而,使用逆转录酶PCR策略未能检测到成熟的κ转录本,这表明存在基质细胞介质,可使前B细胞进展到轻链基因重排但未表达的阶段。逆转录酶PCR进一步显示,在这些细胞中未检测到c-kit(kit配体的受体)和IL-7R的转录本。这表明在细胞经历κ重排时这些受体不再表达,并最小化了基质细胞衍生的kit配体和IL-7在前B细胞向B细胞转变中的作用。