Drexler K, Burtles S, Hurtenbach U
Preclinical Research, Sandoz Pharma, Basel, Switzerland.
Immunol Lett. 1993 Aug;37(2-3):187-96. doi: 10.1016/0165-2478(93)90030-6.
Non-obese-diabetic (NOD) mice spontaneously develop type I diabetes. The disease starts with T cells infiltrating the islets of Langerhans. We therefore examined the T-cell receptor (TCR) V beta region repertoire in islet infiltrates from individual female NOD mice from 4 to 10 week old by polymerase chain reaction (PCR) using V beta 1-V beta 17 specific oligonucleotides. The study revealed a limited heterogeneity of TCR V beta transcripts with a predominance of V beta 1 at the onset of insulitis, i.e. at 4 weeks of age. The TCR VDJ beta sequences of the V beta 1 PCR fragments were identical in most of the individual mice. Among several different mice, similarities in the beta-junctional regions were detected. In contrast, a large heterogeneity of TCR V beta usage was found in mice with advanced insulitis, i.e., from 6 weeks of age on. Thus, these data suggest a limited heterogeneity of TCR V beta usage with a predominance of V beta 1 at the initiation phase of the disease.
非肥胖糖尿病(NOD)小鼠会自发发展为I型糖尿病。该疾病始于T细胞浸润胰岛。因此,我们通过聚合酶链反应(PCR),使用Vβ1 - Vβ17特异性寡核苷酸,检测了4至10周龄的雌性NOD小鼠个体胰岛浸润物中的T细胞受体(TCR)Vβ区域库。研究发现,在胰岛炎发作时,即4周龄时,TCR Vβ转录本的异质性有限,Vβ1占主导。在大多数个体小鼠中,Vβ1 PCR片段的TCR VDJβ序列相同。在几只不同的小鼠中,检测到β连接区域存在相似性。相比之下,在患有晚期胰岛炎的小鼠中,即从6周龄开始,发现TCR Vβ使用情况存在很大的异质性。因此,这些数据表明,在疾病起始阶段,TCR Vβ使用的异质性有限,Vβ1占主导。