Koyasu S, Clayton L K, Lerner A, Heiken H, Parkes A, Reinherz E L
Laboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA, USA.
Int Immunol. 1997 Oct;9(10):1475-80. doi: 10.1093/intimm/9.10.1475.
A rearranged TCR alpha transgene remains transcriptionally inactive in rag-2-/- thymocytes but can be induced by CD3-mediated signals with concomitant maturation of double-negative (DN) thymocytes to the CD4+CD8+ double-positive (DP) stage. Reciprocally, the same signals silence pre-TCR alpha (pT alpha) expression. In normal C57BL/6 thymocytes, TCR alpha expression is not detected in DN thymocytes while, in contrast, TCR beta expression is initiated at the most immature c-kit+CD44+CD25- stage and continues throughout thymocyte development. pT alpha expression is first detected at the intermediate c-kit +/- CD44+CD25+ DN stage, increases during transition to the more mature c-kit-CD44-CD25+ stage and is lost at the DP stage. Thus, although TCR beta and pT alpha expression are independent, the pre-TCR complex mediates signals controlling the appearance of alpha beta TCR through selective regulation of TCR alpha and pT alpha genes.
重排的TCRα转基因在rag-2 -/- 胸腺细胞中保持转录沉默,但可被CD3介导的信号诱导,同时双阴性(DN)胸腺细胞成熟至CD4 + CD8 + 双阳性(DP)阶段。相反,相同的信号使前TCRα(pTα)表达沉默。在正常的C57BL/6胸腺细胞中,DN胸腺细胞中未检测到TCRα表达,而相比之下,TCRβ表达在最不成熟的c-kit + CD44 + CD25 - 阶段开始,并在整个胸腺细胞发育过程中持续。pTα表达首先在中间的c-kit +/- CD44 + CD25 + DN阶段检测到,在向更成熟的c-kit - CD44 - CD25 + 阶段转变期间增加,并在DP阶段消失。因此,尽管TCRβ和pTα表达是独立的,但前TCR复合物通过对TCRα和pTα基因的选择性调节介导控制αβTCR出现的信号。