Tsukada S, Oka Y, Sugiyama H
Third Department of Internal Medicine, Osaka University Medical School, Japan.
Mol Immunol. 1992 Mar;29(3):401-9. doi: 10.1016/0161-5890(92)90028-v.
In SPL2-1-2, a murine B-committed immature cell line transformed with a temperature-sensitive mutant of Abelson virus, T cell receptor (TCR) gamma gene rearrangements, together with IgH gene rearrangements, were induced during culture at a non-permissive temperature (39 degrees C). During 11-12 months of culture, TCR gamma gene rearrangements occurred in all cells. In contrast to TCR gamma genes, neither TCR beta or TCR delta were detected even after 11-12 months of culture at a non-permissive temperature. The majority of the TCR gamma gene rearrangements observed here were V gamma 2 to J gamma 2 joinings and the remaining rearrangements were J gamma 1-linked. V gamma 1 to J gamma 4 and V gamma 3 to J gamma 3 joinings were not detected. Approximately 70% of cells with TCR gamma gene rearrangements produced normal-sized transcripts from the rearranged TCR gamma genes. Cloning and sequencing analysis of a cDNA from the transcripts demonstrated that the whole structure of the cDNA was similar to that of T-lineage cells. These results showed that TCR gene rearrangements were restricted to the gamma genes and that V gamma 2 to J gamma 2 joinings occurred preferentially in this B-committed immature cell line. Furthermore, TCR gamma gene rearrangements also occurred in intracytoplasmic mu-chain producing cells. This indicated that the existence of intracytoplasmic mu-chains did not prevent TCR gamma gene rearrangements, although the existence of mu-chains is known to inhibit further productive IgH gene rearrangements, (allelic exclusion). These results should provide many implications for the mechanism of TCR gene rearrangements, especially that of cross-lineage rearrangements.
在SPL2-1-2(一种用阿贝尔森病毒温度敏感突变体转化的鼠B系未成熟细胞系)中,在非允许温度(39℃)培养期间诱导了T细胞受体(TCR)γ基因重排以及IgH基因重排。在11至12个月的培养过程中,所有细胞均发生了TCRγ基因重排。与TCRγ基因不同,即使在非允许温度下培养11至12个月后,也未检测到TCRβ或TCRδ。这里观察到的大多数TCRγ基因重排是Vγ2与Jγ2连接,其余重排是与Jγ1连锁的。未检测到Vγ1与Jγ4以及Vγ3与Jγ3连接。大约70%具有TCRγ基因重排的细胞从重排的TCRγ基因产生了正常大小的转录本。对转录本的cDNA进行克隆和测序分析表明,该cDNA的整体结构与T系细胞的相似。这些结果表明,TCR基因重排仅限于γ基因,并且在这个B系未成熟细胞系中优先发生Vγ2与Jγ2连接。此外,TCRγ基因重排也发生在产生胞质μ链的细胞中。这表明胞质μ链的存在并不阻止TCRγ基因重排,尽管已知μ链的存在会抑制进一步的有效IgH基因重排(等位基因排斥)。这些结果应为TCR基因重排机制,尤其是跨谱系重排机制提供许多启示。