Held W, Mueller C, MacDonald H R
Department of Pathology, University of Bern, Switzerland.
Eur J Immunol. 1990 Sep;20(9):2133-6. doi: 10.1002/eji.1830200936.
We have analyzed the expression of T cell receptor (TcR) genes in the thymus using in situ RNA hybridizations with probes to the constant regions of the TcR alpha, beta, gamma and delta chains. Localization of transcripts revealed low TcR alpha mRNA levels in the thymus cortex and very low levels in the subcapsular region. In contrast, TcR beta message was very abundant in the cortex. TcR gamma or delta mRNA+ thymocytes showed a scattered, predominantly cortical localization. In contrast to gamma, TcR delta transcripts were abundant in the subcapsular region. Control experiments with sorted TcR alpha/beta or gamma/delta cells revealed a detection efficiency of 75%-85% for the respective TcR mRNA and data on TcR gene expression in mature, CD3+ thymocytes were consistent with previous reports. The analysis of immature, CD3- thymocyte subsets, however, revealed a virtual absence of TcR alpha transcripts and an unexpectedly high proportion of cells (14%-29%) expressing the gene for the TcR delta chain. The data are discussed in view of current models of lineage relationships in the thymus.
我们使用针对T细胞受体(TcR)α、β、γ和δ链恒定区的探针,通过原位RNA杂交分析了胸腺中TcR基因的表达。转录本的定位显示,胸腺皮质中TcRα mRNA水平较低,而在被膜下区域水平极低。相比之下,TcRβ信息在皮质中非常丰富。TcRγ或δ mRNA + 胸腺细胞呈散在分布,主要位于皮质。与γ不同,TcRδ转录本在被膜下区域丰富。对分选的TcRα/β或γ/δ细胞进行的对照实验显示,相应TcR mRNA的检测效率为75%-85%,成熟CD3 + 胸腺细胞中TcR基因表达的数据与先前报道一致。然而,对未成熟CD3 - 胸腺细胞亚群的分析显示,几乎没有TcRα转录本,而表达TcRδ链基因的细胞比例意外地高(14%-29%)。我们根据目前胸腺中谱系关系的模型对这些数据进行了讨论。