Küppers R, Roers A, Kanzler H
Institute for Genetics, University of Cologne, Germany.
Cancer Surv. 1997;30:45-58.
The polymerase chain reaction allows the characterization of RNA and DNA sequences from single cells. Methods were established to analyse single cells isolated from suspension or by multicolour flow cytometry. We established a method to isolate single immunostained cells from frozen tissue sections and to analyse those cells for immunoglobulin gene rearrangements. This method was first used to study B cell differentiation within human germinal centres. In another series of experiments, Hodgkin and Reed-Sternberg (HRS) cells from a total of 14 cases of HD were analysed for B lineage derivation and clonality. In 13 of the 14 cases, clonal V gene rearrangements were identified. This shows that HRS cells generally represent the outgrowth of a clonal population of B cells. The detection of somatic mutations in all VH gene rearrangements amplified from HRS cells and the nature of those mutations identifies a GC B cell as the HRS precursor.
聚合酶链反应可对单细胞的RNA和DNA序列进行特征分析。已建立了从悬浮液中分离或通过多色流式细胞术分析单细胞的方法。我们建立了一种从冷冻组织切片中分离单个免疫染色细胞并分析这些细胞免疫球蛋白基因重排的方法。该方法首先用于研究人类生发中心内的B细胞分化。在另一系列实验中,对总共14例霍奇金淋巴瘤(HD)患者的霍奇金和里德-斯腾伯格(HRS)细胞进行了B系起源和克隆性分析。在14例中的13例中,鉴定出克隆性V基因重排。这表明HRS细胞通常代表B细胞克隆群体的增殖。从HRS细胞扩增的所有VH基因重排中体细胞突变的检测以及这些突变的性质确定GC B细胞为HRS前体。