Kishihara K, Yoshikai Y, Matsuzaki G, Mak T W, Nomoto K
Eur J Immunol. 1987 Apr;17(4):477-82. doi: 10.1002/eji.1830170407.
The expression and sequences of T cell antigen receptor (TcR) alpha and beta-chain genes were investigated in the spleens from congenitally athymic (nude) mice. A small number of Thy-1+ cells (approximately 7.0%) was found in nylon wool-enriched spleen cells from young (8 weeks old) nude mice but no L3T4 or Lyt-2 surface antigens were detected. These nude mice expressed only a low level of 1.0-kb beta-chain mRNA and little or no alpha-gene transcripts. On the other hand the number of Thy-1+ spleen cells increased slightly (to 24%) in old (20 weeks old) nude mice and a small number of L3T4+ (10%) and/or Lyt-2+ (5%) cells were detectable. "Full length" 1.7-kb alpha-chain and 1.3-kb beta-chain messages could be found in nylon wool-enriched spleen cells from old nude mice. Sequence analysis of the cDNA revealed that no functional alpha and beta-chain genes can be detected in the spleen cells of young athymic mice while some of the old mice with nu/nu genotype are composed of completely rearranged V-(D)-J-C-gene segments which encode potentially functional proteins. Interestingly, two of three independent cDNA clones encoding the alpha chain used the same V alpha and J alpha-gene segments. These results suggest that extrathymic TcR alpha and beta-chain gene rearrangements do occur, though slowly, to some extent, in nude mice and may be responsible for the limited antigen and/or H-2-related T cell functions in these old athymic mice. The data further suggests that the TcR repertoire in athymic mice may also be limited.
对先天性无胸腺(裸)小鼠脾脏中T细胞抗原受体(TcR)α和β链基因的表达及序列进行了研究。在幼年(8周龄)裸小鼠经尼龙毛富集的脾细胞中发现少量Thy-1+细胞(约7.0%),但未检测到L3T4或Lyt-2表面抗原。这些裸小鼠仅表达低水平的1.0 kbβ链mRNA,几乎没有或没有α基因转录本。另一方面,老年(20周龄)裸小鼠中Thy-1+脾细胞数量略有增加(至24%),可检测到少量L3T4+(10%)和/或Lyt-2+(5%)细胞。在老年裸小鼠经尼龙毛富集的脾细胞中可发现“全长”1.7 kbα链和1.3 kbβ链信息。cDNA序列分析显示,在幼年无胸腺小鼠的脾细胞中未检测到功能性α和β链基因,而一些nu/nu基因型的老年小鼠由完全重排的V-(D)-J-C基因片段组成,这些片段编码潜在的功能性蛋白质。有趣的是,编码α链的三个独立cDNA克隆中有两个使用相同的Vα和Jα基因片段。这些结果表明,在裸小鼠中,胸腺外TcRα和β链基因重排确实会在一定程度上缓慢发生,这可能是这些老年无胸腺小鼠中有限的抗原和/或H-2相关T细胞功能的原因。数据进一步表明,无胸腺小鼠中的TcR库也可能有限。