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

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Bleomycin / pharmacology*
  • Cell Adhesion Molecules / genetics
  • Chemokines / genetics
  • Extracellular Matrix Proteins / genetics
  • Gene Deletion
  • Gene Expression Profiling*
  • Inflammation / chemically induced
  • Inflammation / genetics
  • Inflammation / immunology
  • Mice
  • Proto-Oncogene Proteins c-fos / deficiency
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / metabolism*
  • Pulmonary Fibrosis / chemically induced*
  • Pulmonary Fibrosis / genetics*
  • Pulmonary Fibrosis / immunology
  • Receptors, Chemokine / genetics
  • Time Factors
  • Transcription Factor AP-1 / metabolism*

Substances

  • Cell Adhesion Molecules
  • Chemokines
  • Extracellular Matrix Proteins
  • Proto-Oncogene Proteins c-fos
  • Receptors, Chemokine
  • Transcription Factor AP-1
  • fos-related antigen 1
  • Bleomycin