Gibbons D, Douglas N C, Barber D F, Liu Q, Sullo R, Geng L, Fehling H J, von Boehmer H, Hayday A C
Guy's King's St. Thomas' Medical School, Guy's Hospital, London Bridge, London SE1 9RT, United Kingdom.
J Exp Med. 2001 Sep 3;194(5):695-703. doi: 10.1084/jem.194.5.695.
beta selection is a major checkpoint in early thymocyte differentiation, mediated by successful expression of the pre-T cell receptor (TCR) comprising the TCRbeta chain, CD3 proteins, and a surrogate TCRalpha chain, pTalpha. The mechanism of action of the pre-TCR is unresolved. In humans and mice, the pTalpha gene encodes two RNAs, pTalpha(a), and a substantially truncated form, pTalpha(b). This study shows that both are biologically active in their capacity to rescue multiple thymocyte defects in pTalpha(-/-) mice. Further active alleles of pTalpha include one that lacks both the major ectodomain and much of the long cytoplasmic tail (which is unique among antigen receptor chains), and another in which the cytoplasmic tail is substituted with the short tail of TCR Calpha. Thus, very little of the pTalpha chain is required for function. These data support a hypothesis that the primary role of pTalpha is to stabilize the pre-TCR, and that much of the conserved structure of pTalpha probably plays a critical regulatory role.
β选择是早期胸腺细胞分化中的一个主要检查点,由前T细胞受体(TCR)的成功表达介导,该受体由TCRβ链、CD3蛋白和替代TCRα链pTα组成。前TCR的作用机制尚未明确。在人类和小鼠中,pTα基因编码两种RNA,pTα(a)和一种大幅截短的形式pTα(b)。本研究表明,二者在挽救pTα(-/-)小鼠多种胸腺细胞缺陷的能力方面均具有生物学活性。pTα的其他活性等位基因包括一个既缺少主要胞外结构域又缺少大部分长细胞质尾巴(这在抗原受体链中是独特的)的等位基因,以及另一个细胞质尾巴被TCRα的短尾巴替代的等位基因。因此,pTα链发挥功能所需极少。这些数据支持了一个假说,即pTα的主要作用是稳定前TCR,并且pTα的许多保守结构可能起着关键的调节作用。