Woolf Eilon, Xiao Cuiying, Fainaru Ofer, Lotem Joseph, Rosen Dalia, Negreanu Varda, Bernstein Yael, Goldenberg Dalia, Brenner Ori, Berke Gideon, Levanon Ditsa, Groner Yoram
Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot 76100, Israel.
Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7731-6. doi: 10.1073/pnas.1232420100. Epub 2003 Jun 9.
The RUNX transcription factors are important regulators of lineage-specific gene expression. RUNX are bifunctional, acting both as activators and repressors of tissue-specific target genes. Recently, we have demonstrated that Runx3 is a neurogenic transcription factor, which regulates development and survival of proprioceptive neurons in dorsal root ganglia. Here we report that Runx3 and Runx1 are highly expressed in thymic medulla and cortex, respectively, and function in development of CD8 T cells during thymopoiesis. Runx3-deficient (Runx3 KO) mice display abnormalities in CD4 expression during lineage decisions and impairment of CD8 T cell maturation in the thymus. A large proportion of Runx3 KO peripheral CD8 T cells also expressed CD4, and in contrast to wild-type, their proliferation ability was largely reduced. In addition, the in vitro cytotoxic activity of alloimmunized peritoneal exudate lymphocytes was significantly lower in Runx3 KO compared with WT mice. In a compound mutant mouse, null for Runx3 and heterozygous for Runx1 (Runx3-/-;Runx1+/-), all peripheral CD8 T cells also expressed CD4, resulting in a complete lack of single-positive CD8+ T cells in the spleen. The results provide information on the role of Runx3 and Runx1 in thymopoiesis and suggest that both act as transcriptional repressors of CD4 expression during T cell lineage decisions.
RUNX转录因子是谱系特异性基因表达的重要调节因子。RUNX具有双重功能,既作为组织特异性靶基因的激活因子,又作为其抑制因子。最近,我们证明Runx3是一种神经源性转录因子,可调节背根神经节中本体感觉神经元的发育和存活。在此我们报告,Runx3和Runx1分别在胸腺髓质和皮质中高表达,并在胸腺细胞生成过程中对CD8 T细胞的发育起作用。Runx3缺陷型(Runx3 KO)小鼠在谱系决定过程中CD4表达出现异常,且胸腺中CD8 T细胞成熟受损。很大一部分Runx3 KO外周CD8 T细胞也表达CD4,与野生型相比,它们的增殖能力大幅降低。此外,与野生型小鼠相比,Runx3 KO同种异体免疫腹膜渗出淋巴细胞的体外细胞毒性活性显著降低。在一种复合突变小鼠中,Runx3基因敲除且Runx1基因杂合(Runx3-/-;Runx1+/-),所有外周CD8 T细胞均表达CD4,导致脾脏中完全缺乏单阳性CD8+ T细胞。这些结果提供了关于Runx3和Runx1在胸腺细胞生成中作用的信息,并表明二者在T细胞谱系决定过程中均作为CD4表达的转录抑制因子发挥作用。