Rogge L, Bianchi E, Biffi M, Bono E, Chang S Y, Alexander H, Santini C, Ferrari G, Sinigaglia L, Seiler M, Neeb M, Mous J, Sinigaglia F, Certa U
Roche Milano Ricerche, Milano, Italy.
Nat Genet. 2000 May;25(1):96-101. doi: 10.1038/75671.
Many pathological processes, including those causing allergies and autoimmune diseases, are associated with the presence of specialized subsets of T helper cells at the site of inflammation. Understanding the genetic program that controls the functional properties of T helper type 1 (Th1) versus T helper type 2 (Th2) cells may provide insight into the pathophysiology of inflammatory diseases. We compared the gene-expression profiles of human Th1 and Th2 cells using high-density oligonucleotide arrays with the capacity to display transcript levels of 6,000 human genes. Here we analyse the data sets derived from five independent experiments using statistical algorithms. This approach resulted in the identification of 215 differentially expressed genes, encoding proteins involved in transcriptional regulation, apoptosis, proteolysis, and cell adhesion and migration. A subset of these genes was further upregulated by exposure of differentiated Th1 cells to interleukin-12 (IL-12), as confirmed by kinetic PCR analysis, indicating that IL-12 modulates the effector functions of Th1 cells in the absence of antigenic stimulation. Functional assays and in vivo expression of selected genes have validated the biological relevance of our study. Our results provide new insight into the transcriptional program controlling the functional diversity of subsets of T helper cells.
许多病理过程,包括那些引发过敏和自身免疫性疾病的过程,都与炎症部位存在特定的辅助性T细胞亚群有关。了解控制1型辅助性T细胞(Th1)与2型辅助性T细胞(Th2)功能特性的基因程序,可能有助于深入了解炎症性疾病的病理生理学。我们使用能够显示6000个人类基因转录水平的高密度寡核苷酸阵列,比较了人类Th1和Th2细胞的基因表达谱。在此,我们使用统计算法分析了来自五个独立实验的数据集。这种方法导致鉴定出215个差异表达基因,这些基因编码参与转录调控、凋亡、蛋白水解以及细胞黏附和迁移的蛋白质。通过实时定量PCR分析证实,分化的Th1细胞暴露于白细胞介素-12(IL-12)后,这些基因中的一部分进一步上调,这表明在没有抗原刺激的情况下,IL-12调节Th1细胞的效应功能。功能测定和所选基因的体内表达验证了我们研究的生物学相关性。我们的结果为控制辅助性T细胞亚群功能多样性的转录程序提供了新的见解。