Chang Hua-Chen, Zhang Shangming, Thieu Vivian T, Slee Roger B, Bruns Heather A, Laribee R Nicholas, Klemsz Michael J, Kaplan Mark H
Department of Microbiology and Immunology, and Walther Oncology Center, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Immunity. 2005 Jun;22(6):693-703. doi: 10.1016/j.immuni.2005.03.016.
Primary T helper 2 cells are heterogeneous, expressing subsets of cytokines at varying levels. Mechanisms controlling this spectrum of phenotypes are still unclear. The ETS family transcription factor PU.1 is expressed in Th2 but not Th1 cells. Th2 cytokine production is decreased in cultures transduced with a PU.1-expressing retrovirus and increased in Th2 cells following RNAi that decreases PU.1 expression. In primary cultures, PU.1 expression is restricted to a subpopulation of Th2 cells that express CCL22 and a subset of Th2 cytokines. PU.1 regulates the Th2 phenotype by interfering with GATA-3 DNA binding without altering GATA-3 protein levels. Thus, the expression of PU.1 in subsets of Th2 cells establishes a defined cytokine profile and contributes towards establishing the spectrum of cytokine production observed in Th2 populations.
初始辅助性T2细胞具有异质性,不同水平表达多种细胞因子亚群。控制这种表型谱的机制仍不清楚。ETS家族转录因子PU.1在Th2细胞而非Th1细胞中表达。在用表达PU.1的逆转录病毒转导的培养物中,Th2细胞因子的产生减少,而在RNA干扰降低PU.1表达后的Th2细胞中则增加。在原代培养中,PU.1的表达局限于表达CCL22的Th2细胞亚群和一部分Th2细胞因子。PU.1通过干扰GATA-3与DNA的结合来调节Th2表型,而不改变GATA-3蛋白水平。因此,PU.1在Th2细胞亚群中的表达建立了特定的细胞因子谱,并有助于建立在Th2群体中观察到的细胞因子产生谱。