Yasui D H, Genetta T, Kadesch T, Williams T M, Swain S L, Tsui L V, Huber B T
Department of Pathology, Tufts University School of Medicine, Boston, MA 02111, USA.
J Immunol. 1998 May 1;160(9):4433-40.
Th1- and Th2-type cells mediate distinct effector functions via cytokine secretion in response to immunologic challenge. Precursor Th cells transcribe IFN-gamma, IL-2, and IL-4 upon activation. Repeated stimulation of Th precursor cells in the presence of IL-4 leads to terminally differentiated Th2 cells that have lost the ability to transcribe the IL-2 gene. We provide evidence that repression of IL-2 gene expression in Th2 cells and partial repression in Th1 cells are mediated by ZEB, a zinc finger, E box-binding transcription factor. This factor binds to a negative regulatory element, NRE-A, in the IL-2 promoter, thereby acting as a potent repressor of IL-2 transcription.
Th1型和Th2型细胞通过分泌细胞因子介导不同的效应功能,以应对免疫挑战。前体Th细胞在激活后转录干扰素-γ、白细胞介素-2和白细胞介素-4。在白细胞介素-4存在的情况下反复刺激Th前体细胞会导致终末分化的Th2细胞,这些细胞失去了转录白细胞介素-2基因的能力。我们提供的证据表明,Th2细胞中白细胞介素-2基因表达的抑制以及Th1细胞中的部分抑制是由ZEB介导的,ZEB是一种锌指、E盒结合转录因子。该因子与白细胞介素-2启动子中的负调控元件NRE-A结合,从而作为白细胞介素-2转录的有效抑制因子。