Monticelli Silvia, Rao Anjana
Department of Pathology, Harvard Medical School, and The Center for Blood Research, Alpert Building Rm. 152, 200 Longwood Avenue, Boston, MA 02115, USA.
Eur J Immunol. 2002 Oct;32(10):2971-8. doi: 10.1002/1521-4141(2002010)32:10<2971::AID-IMMU2971>3.0.CO;2-G.
The nuclear factor of activated T cells (NFAT) plays a key role in gene transcription in both immune and non-immune cell types. Genetic ablation of individual NFAT proteins produces complex phenotypes in mice; in particular, NFAT1(-/-) and NFAT2(-/-) T cells show overproduction and underproduction of IL-4, respectively. We have taken a positive approach to the question of whether these two NFAT family members differentially regulate IL-4 gene transcription. Using constitutively-active NFAT proteins with alanine substitutions instead of phosphorylated serine residues in the regulatory domain, we find that NFAT1 and NFAT2 are both positive regulators of IL-4 gene transcription, intrinsically very similar in their ability to induce and sustain transcription of the IL-4 gene. Thus the disparate phenotypes of NFAT1(-/-) and NFAT2(-/-) T cells do not reflect differences in DNA-binding or transcriptional activity at the IL-4 gene, but most likely arise from differential regulation of the two proteins or other indirect effects.
活化T细胞核因子(NFAT)在免疫细胞和非免疫细胞类型的基因转录中起关键作用。单个NFAT蛋白的基因敲除在小鼠中产生复杂的表型;特别是,NFAT1(-/-)和NFAT2(-/-) T细胞分别显示出IL-4的过量产生和产生不足。我们采用了一种积极的方法来研究这两个NFAT家族成员是否差异调节IL-4基因转录的问题。使用在调节域中具有丙氨酸取代而非磷酸化丝氨酸残基的组成型活性NFAT蛋白,我们发现NFAT1和NFAT2都是IL-4基因转录的正调节因子,在诱导和维持IL-4基因转录的能力上本质上非常相似。因此,NFAT1(-/-)和NFAT2(-/-) T细胞的不同表型并不反映IL-4基因在DNA结合或转录活性上的差异,而很可能源于这两种蛋白的差异调节或其他间接效应。