Division of Developmental Biology and Basic Research, Department of Pediatrics, University of Illinois at Chicago, Chicago, IL 60612, USA.
BMC Genomics. 2013 Jun 7;14:381. doi: 10.1186/1471-2164-14-381.
The Fra-1/AP-1 transcription factor regulates the expression of genes controlling various processes including migration, invasion, and survival as well as extracellular remodeling. We recently demonstrated that loss of Fra-1 leads to exacerbated bleomycin-induced pulmonary fibrosis, accompanied by enhanced expression of various inflammatory and fibrotic genes. To better understand the molecular mechanisms by which Fra-1 confers protection during bleomycin-induced lung injury, genome-wide mRNA expression profiling was performed.
We found that Fra-1 regulates gene expression programs that include: 1) several cytokines and chemokines involved in inflammation, 2) several genes involved in the extracellular remodeling and cell adhesion, and 3) several genes involved in programmed cell death.
Loss of Fra-1 leads to the enhanced expression of genes regulating inflammation and immune responses and decreased the expression of genes involved in apoptosis, suggesting that this transcription factor distinctly modulates early pro-fibrotic cellular responses.
Fra-1/AP-1 转录因子调节控制各种过程(包括迁移、侵袭和存活以及细胞外重塑)的基因表达。我们最近证明,Fra-1 的缺失会导致博来霉素诱导的肺纤维化加重,同时伴有各种炎症和纤维化基因的表达增强。为了更好地了解 Fra-1 在博来霉素诱导的肺损伤过程中提供保护的分子机制,进行了全基因组 mRNA 表达谱分析。
我们发现 Fra-1 调节包括以下几种基因表达程序:1)几种参与炎症的细胞因子和趋化因子,2)几种参与细胞外重塑和细胞黏附的基因,3)几种参与程序性细胞死亡的基因。
Fra-1 的缺失导致调节炎症和免疫反应的基因表达增强,而参与细胞凋亡的基因表达减少,这表明该转录因子明显调节早期促纤维化的细胞反应。