Cao Wuxiong, Chen Yangde, Alkan Sefik, Subramaniam Arun, Long Fan, Liu Hong, Diao Rong, Delohery Thomas, McCormick Jason, Chen Rong, Ni Donghui, Wright Paul S, Zhang Xin, Busch Steve, Zilberstein Asher
Aventis Pharmaceuticals, Bridgewater, NJ 07059, USA.
Eur J Immunol. 2005 Sep;35(9):2709-17. doi: 10.1002/eji.200425957.
Upon activation in vitro, only a fraction of the bulk human T helper cell cultures secret the hallmark Th1/2 cytokines (IFN-gamma for Th1 and IL-4 for Th2, respectively). It is uncertain whether these IFN-gamma-/IL-4- cells are differentiated Th1 or Th2 cells. Here, we have characterized live IFN-gamma+, IL-4+ and IFN-gamma-/IL-4- cells isolated from Th cell cultures treated under Th1 or Th2 polarizing conditions by employing affinity matrix capture technology. RNA samples from the sorted cells were analyzed by real time RT-PCR and microarrays. The double negative cells from either Th1 or Th2 cultures expressed lower levels of Th1/Th2 marker cytokine genes (IFNgamma, IL4, and IL5). However, they were comparable with the IFN-gamma+ or IL-4+ cells in the expression levels of other Th1/Th2 marker genes (GATA3, Tbet, and IL12Rbeta2). Most importantly, these double negative cells were already committed in their Th1/Th2 lineages. Gene expression profiling analysis showed that very few previously identified Th1/Th2 marker genes were differentially expressed between the IFN-gamma or IL-4 producers and the non-producers, further underscoring the similarity between these two groups.
在体外激活后,大量人类辅助性T细胞培养物中只有一小部分分泌标志性的Th1/Th2细胞因子(分别为Th1的IFN-γ和Th2的IL-4)。这些IFN-γ-/IL-4-细胞是否为分化的Th1或Th2细胞尚不确定。在此,我们利用亲和基质捕获技术对在Th1或Th2极化条件下处理的Th细胞培养物中分离出的活的IFN-γ+、IL-4+和IFN-γ-/IL-4-细胞进行了表征。通过实时RT-PCR和微阵列分析分选细胞的RNA样本。来自Th1或Th2培养物的双阴性细胞表达较低水平的Th1/Th2标记细胞因子基因(IFNγ、IL4和IL5)。然而,它们在其他Th1/Th2标记基因(GATA3、Tbet和IL12Rβ2)的表达水平上与IFN-γ+或IL-4+细胞相当。最重要的是,这些双阴性细胞已经确定了它们的Th1/Th2谱系。基因表达谱分析表明,在IFN-γ或IL-4产生细胞与非产生细胞之间,很少有先前确定的Th1/Th2标记基因存在差异表达,这进一步强调了这两组细胞之间的相似性。