Robijn R J, Bloemendal H, Jainandunsing S, Wiegman L J, VanBerge-Henegouwen G P, Logtenberg T, Koningsberger J C
Department of Gastroenterology, University Hospital Utrecht, The Netherlands.
Scand J Immunol. 1993 Sep;38(3):247-53. doi: 10.1111/j.1365-3083.1993.tb01721.x.
We have performed a phenotypic and molecular analysis of monoclonal TCR gamma/delta T-cell lines derived from jejunal and colonic biopsies of healthy individuals. Flow cytometric analysis employing a panel of 24 monoclonal antibodies (MoAbs) demonstrated that intestinal TCR gamma/delta intraepithelial lymphocytes (IEL) constitute a phenotypically heterogeneous population. Nucleotide sequence analysis of expressed TCR delta variable (V) regions revealed the dominant utilization of the V delta 2 and D delta 3 gene segments and frequent rearrangement of J delta 3. IEL V delta regions displayed extensive junctional diversity as a result of N and P insertion and the utilization of D delta 3 in all three reading frames. The results demonstrate that intestinal TCR gamma/delta T cells from healthy individuals constitute a phenotypically heterogeneous population expressing V delta regions that differ from their systemic counterparts.
我们对从健康个体的空肠和结肠活检组织中获得的单克隆TCRγ/δ T细胞系进行了表型和分子分析。使用一组24种单克隆抗体(MoAbs)进行的流式细胞术分析表明,肠道TCRγ/δ上皮内淋巴细胞(IEL)构成了一个表型异质性群体。对表达的TCRδ可变(V)区进行核苷酸序列分析,结果显示Vδ2和Dδ3基因片段占主导地位,且Jδ3频繁重排。由于N和P插入以及在所有三个阅读框中对Dδ3的利用,IEL Vδ区表现出广泛的连接多样性。结果表明,来自健康个体的肠道TCRγ/δ T细胞构成了一个表型异质性群体,其表达的Vδ区与其全身对应物不同。