posted on 2014-01-06, 00:00authored bySubbiah Rajasekaran, Wei Zhang, Narsa M. Reddy, Sekhar P. Reddy
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.
Funding
This study was supported by grants from
the NIH (RO1 ES11863, RO1 HL66109, and R21 ES18998) and Flight
Attendents Medical Research Institute (FAMRI) to SPR.