The excessive accumulation of collagen is the hallmark of idiopathic pulmonary fibrosis (IPF). The knowledge of the factors and mechanisms that limit the production of collagen are central to our understanding of the normal balance of matrix deposition and pathologic fibrosis. We demonstrated that interleukin 1beta, (IL-1beta) tumor necrosis factor alpha (TNFalpha) and prostaglandins (PG) reduce the production of type I collagen by normal (NL) human lung fibroblasts by transcriptional regulation. We have preliminary evidence of an altered response of lung fibroblasts from patients with IPF to these cytokines in terms of collagen and PG production. The elements involved in the inhibition of the transcription of the type I procollagen genes by IL-1beta, TNFalpha, and PG have not been defined. The hypothesis to be tested here is that there is a defective regulation of the expression of the alpha(I) procollagen gene by IL-1beta, TNFalpha, and PG in IPF fibroblasts. To test this hypothesis we will pursue 3 main objectives: First, we will further define the participation of endogenous PG on IL-1beta, TNFalpha: and transforming growth factor beta1 (TGFbeta1) effects on collagen gene expression in IPF fibroblasts at the protein, mRNA, and transcriptional levels; second, we will identify cis- and trans-acting elements involved IL-1beta, TNFalpha and PG down-regulation of transcription of the alpha1(I) procollagen gene promoter by transfections with promoter-reporter constructs and reporter assays, and identify DNA binding proteins and confirm the functionality of the cis-elements by site directed mutagenesis; and third, we will identify alterations of the cis- and trans-acting elements involved in PGE2, IL- 1beta and TNFalpha inhibition of transcription of the alpha1(I) procollagen promoter in IPF fibroblasts. We expect that the application of advanced methods of molecular biology will allow the elucidation of the role that PG, IL-1beta, and TNFalpha may play in the pathogenesis of the severe fibrotic process occurring in the lung in patients with IPF.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Minority School Faculty Development Awards (K14)
Project #
1K14HL003159-01
Application #
2211244
Study Section
Special Emphasis Panel (ZHL1-CCT-L (F1))
Project Start
1994-08-01
Project End
1999-06-30
Budget Start
1994-08-01
Budget End
1995-06-30
Support Year
1
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
061197161
City
Philadelphia
State
PA
Country
United States
Zip Code
19107