Hernández-Hoyos Gabriela, Anderson Michele K, Wang Chi, Rothenberg Ellen V, Alberola-Ila Jose
Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125, USA.
Immunity. 2003 Jul;19(1):83-94. doi: 10.1016/s1074-7613(03)00176-6.
GATA-3 is expressed at higher levels in CD4 than in CD8 SP thymocytes. Here we show that upregulation of GATA-3 expression in DP thymocytes is triggered by TCR stimulation, and the extent of upregulation correlates with the strength of the TCR signal. Overexpression of GATA-3 or a partial GATA-3 agonist during positive selection inhibits CD8 SP cell development but is not sufficient to divert class I-restricted T cell precursors to the CD4 lineage. Conversely, expression of the GATA-3 antagonist ROG or of a GATA-3 siRNA hairpin markedly enhances development of CD8 SP cells and reduces CD4 SP development. We propose that GATA-3 contributes to linking the TCR signal strength to the differentiation program of CD4 and CD8 thymocytes.
GATA-3在CD4单阳性胸腺细胞中的表达水平高于CD8单阳性胸腺细胞。我们在此表明,双阳性胸腺细胞中GATA-3表达的上调是由TCR刺激触发的,上调程度与TCR信号强度相关。在阳性选择过程中过表达GATA-3或部分GATA-3激动剂会抑制CD8单阳性细胞的发育,但不足以将I类限制性T细胞前体转向CD4谱系。相反,GATA-3拮抗剂ROG或GATA-3 siRNA发夹的表达显著增强了CD8单阳性细胞的发育并减少了CD4单阳性细胞的发育。我们提出,GATA-3有助于将TCR信号强度与CD4和CD8胸腺细胞的分化程序联系起来。