Mononuclear cells (MC) are important regulators of the fibrotic response, in part through their elaboration of inflammatory cytokines. It is known that fibroblast proliferation is regulated by a complex cascade of cytokine interactions with the interferons (IFN), interleukin-1 family of proteins (IL-1), tumor necrosis factor (TNF), interleukin-6 (IL-6) and transforming growth factor-beta (TGF-beta) playing important roles. Mononuclear cells are also known to elaborate soluble factors that stimulate and inhibit fibroblast collagen production and degradation. However, little has been done to define the interactions of these cytokines that are important in regulating collagen accumulation and to determine the molecular mechanisms of these effects. Thus, we plan: 1. To characterize further the effects of recombinant (r) IFNs (gamma and beta), rTNF, rIL-1 (alpha and beta), rIL-6 and TGF-B on lung fibroblast collagen production. The cytokines will be tested individually and in combination to define cytokine-cytokine synergy. Their effect on types I, III, IV and V collagen synthesis will be assessed and compared to their effects on fibronectin synthesis. 2. To characterize the human gene for the tissue inhibitor of mettalloproteinase (TIMP). The initial and rate limiting step in the degradation of collagen is cleavage by collagenase. Collagenase activity is modulated by inhibitors such as TIMP. We have obtained clones encompassing the 5' portion, which probably includes the promoter region, of the human TIMP gene. The gene needs to be characterized in order to define elements which control expression of the gene, including those responsive to cytokines. 3. To charcterize the effect of IFNs (gamma and beta), rTNF, rIL-1 (alpha and beta) rIL-6 and TGF-B on fibroblast production of collagenase and TIMP. The cytokines will be tested individually and in combination. 4. To characterize the molecular mechanisms of the regulatory effects of cytokines on matrix production. Molecular biology techniques will be used to define whether these regulatory events are acting at the level of transcription, mRNA stability or translation and investigate how these processes are altered.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL041216-06
Application #
3358827
Study Section
Special Emphasis Panel (SRC (17))
Project Start
1991-01-01
Project End
1993-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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