Makino Y, Yamagata N, Sasho T, Adachi Y, Kanno R, Koseki H, Kanno M, Taniguchi M
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
J Exp Med. 1993 May 1;177(5):1399-408. doi: 10.1084/jem.177.5.1399.
It is known that rearrangement of the T cell antigen receptor (TCR) gene occurs in the thymus during T cell development and consequently results both in the deletion of DNA between the variable (V) and diversity/joining segments and in the formation of a circular DNA with recombination signal sequences. Here, we provide evidence that V alpha 14+ TCR gene rearrangements take place in extrathymic sites, such as bone marrow, liver, and intestine, but not in spleen, because we were able to detect frequent productive and nonproductive V alpha 14+ coding and signal sequences as a result of TCR rearrangements in extrathymic sites. Similar findings were also detected in athymic mice. Quantitative analysis shows that the relative amounts of V alpha 14 gene-mediated signal sequences in extrathymic tissues are higher than those in thymus. On the contrary, TCR rearrangements of V alpha 1.1 T cells, which are known to develop in the thymus, were mainly detected in the thymus, Peyer's patch, and spleen, but not in other extrathymic tissues, showing patterns distinct from V alpha 14 TCR rearrangements. These findings are evidence of extrathymic development of V alpha 14+ T cells. Differential characteristic TCR rearrangement patterns also indicate that distinct TCR repertoires are generated in different lymphoid tissues.
已知T细胞抗原受体(TCR)基因重排在胸腺中T细胞发育过程中发生,从而导致可变区(V)与多样性/连接区之间的DNA缺失,并形成带有重组信号序列的环状DNA。在此,我们提供证据表明Vα14⁺ TCR基因重排在胸腺外部位发生,如骨髓、肝脏和肠道,但不在脾脏中发生,因为我们能够在胸腺外部位检测到由于TCR重排而频繁出现的有功能和无功能的Vα14⁺编码序列和信号序列。在无胸腺小鼠中也检测到了类似的结果。定量分析表明,胸腺外组织中Vα14基因介导的信号序列的相对量高于胸腺中的相对量。相反,已知在胸腺中发育的Vα1.1 T细胞的TCR重排主要在胸腺、派氏结和脾脏中检测到,而不在其他胸腺外组织中,显示出与Vα14 TCR重排不同的模式。这些发现证明了Vα14⁺ T细胞的胸腺外发育。不同特征的TCR重排模式还表明,在不同的淋巴组织中产生了不同的TCR库。