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Fra-1/AP-1 转录因子调控的基因在博来霉素诱导肺纤维化过程中的表达谱。

Expression profiling of genes regulated by Fra-1/AP-1 transcription factor during bleomycin-induced pulmonary fibrosis.

机构信息

Division of Developmental Biology and Basic Research, Department of Pediatrics, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

BMC Genomics. 2013 Jun 7;14:381. doi: 10.1186/1471-2164-14-381.

Abstract

BACKGROUND

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

结果

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。

结论

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。

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