Spiess S, Kuhröber A, Schirmbeck R, Arden B, Reimann J
Institute of Microbiology, University of Ulm, Germany.
Immunology. 1993 Feb;78(2):252-9.
CD3+ cells are detectable in bone marrow of athymic mice homozygous for the nude mutation. As previously shown, cells expressing the gamma delta T-cell receptor (TcR) represent 30-40% of this T-cell population. Using V delta-specific, V alpha 4-specific, and C delta-specific primers, TcR delta-chain transcripts were reverse transcribed and polymerase chain reaction (PCR)-amplified from total RNA prepared from bone marrow cells (BMC) of 6-month-old NMRI nu/nu mice. Amplified TcR delta-chain cDNA was cloned, and 49 randomly selected clones derived from seven amplification reactions were sequenced. Sequence analyses showed: (1) more than 80% of the sequenced clones represented in-frame transcripts of the TcR delta-chain; (2) in-frame transcripts containing V delta 1-, V delta 2-, V delta 3-, V delta 4-, V delta 5-, V delta 6- and V alpha 4-gene segments were detectable in nude BMC; (3) V delta 2-, V delta 4- and V delta 5-containing transcripts were more abundant and more diverse than V delta 1- and V delta 3-containing transcripts; (4) extensive N-region diversity was present in the V delta-D delta 2 (N1), D delta 2-D delta 1 (N2) and D delta 1-J delta 1 (N3) junctional regions; (5) P nucleotide additions were present in many transcripts; and (6) unusual truncated, in-frame transcripts with deleted D- and J-region genes were detected. A large potential TcR delta-chain repertoire is thus present in nude BMC.
在纯合裸突变的无胸腺小鼠的骨髓中可检测到CD3 +细胞。如先前所示,表达γδ T细胞受体(TcR)的细胞占该T细胞群体的30-40%。使用Vδ特异性、Vα4特异性和Cδ特异性引物,从6个月大的NMRI nu/nu小鼠的骨髓细胞(BMC)制备的总RNA中逆转录TcRδ链转录本并进行聚合酶链反应(PCR)扩增。扩增的TcRδ链cDNA被克隆,并对来自七个扩增反应的49个随机选择的克隆进行测序。序列分析表明:(1)超过80%的测序克隆代表TcRδ链的框内转录本;(2)在裸BMC中可检测到含有Vδ1- Vδ2-、Vδ3-、Vδ4-、Vδ5-、Vδ6-和Vα4基因片段的框内转录本;(3)含有Vδ2-、Vδ4-和Vδ5的转录本比含有Vδ1-和Vδ3的转录本更丰富、更多样化;(4)在Vδ-Dδ2(N1)、Dδ2-Dδ1(N2)和Dδ1-Jδ1(N3)连接区域存在广泛的N区域多样性;(5)许多转录本中存在P核苷酸添加;(6)检测到具有缺失D和J区域基因的异常截短的框内转录本。因此,裸BMC中存在大量潜在的TcRδ链库。