Rothenberg Ellen V
Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125, USA.
Semin Immunol. 2002 Dec;14(6):431-40. doi: 10.1016/s1044532302000787.
T lymphocytes originate from pluripotent precursors and undergo lasting commitment to the T cell developmental fate during their processing in the thymus. Commitment includes both the acquisition of essential T cell characteristics and the foreclosing of other developmental options. Gain of T cell characteristics is probably mediated by separate mechanisms, at least in detail, from loss of alternative developmental potentials. Programmed shifts in survival requirements make changes irreversible. Here we review the current evidence identifying the regulatory components of this commitment pathway, and the first hints of how they work together. Roles for PU.1, GATA-3, and their target genes are highlighted.
T淋巴细胞起源于多能前体细胞,并在胸腺中发育过程中对T细胞的发育命运做出持久的定向决定。定向决定包括获得基本的T细胞特征以及排除其他发育选择。获得T细胞特征可能至少在细节上是由与丧失其他发育潜能不同的机制介导的。生存需求的程序性转变使变化不可逆转。在这里,我们综述了目前确定这一定向决定途径调控成分的证据,以及它们如何协同作用的初步线索。重点介绍了PU.1、GATA-3及其靶基因的作用。