Interferon-gamma upregulates the stromelysin-1 gene expression by human skin fibroblasts in culture.
- Author:
Kyu Suk LEE
1
;
Young Wook RYOO
;
Joon Young SONG
Author Information
1. Department of Dermatology, Keimyung University School of Medicine, Taegu, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
stromelysin-1;
interferon-g;
AP-1;
gene expression
- MeSH:
Cell Nucleus;
Cells, Cultured;
Chloramphenicol O-Acetyltransferase/metabolism;
Chloramphenicol O-Acetyltransferase/genetics;
Collagenases/genetics;
Collagenases/drug effects;
Fibroblasts/metabolism;
Fibroblasts/drug effects*;
Gene Expression Regulation/drug effects;
Human;
Interferon Type II/pharmacology*;
Promoter Regions (Genetics);
Recombinant Proteins/metabolism;
Recombinant Proteins/genetics;
Skin/cytology*;
Stromelysin 1/metabolism*;
Stromelysin 1/genetics*;
Stromelysin 1/drug effects;
Transcription Factor AP-1/metabolism;
Transcription, Genetic;
Transforming Growth Factor beta/pharmacology;
Up-Regulation (Physiology)
- From:Experimental & Molecular Medicine
1998;30(2):59-64
- CountryRepublic of Korea
- Language:English
-
Abstract:
The equilibrium between deposition and degradation of extracellular matrix(ECM) is essential to normal tissue development and repair of wound or inflammatory responses. It has recently become apparent that several cytokines and growth factors are capable of modulating fibroblast proliferation and biosynthetic activity. To understand the role of these factors in connective tissue regulation, we examined the effect of interferon-gamma (IFN-gamma) on stromelysin-1 gene expression in cultured human dermal fibroblasts. The steady-state levels of stromelysin-1 mRNA were increased in IFN-gamma treated cultured dermal fibroblasts. In the CAT assay, the stromelysin-1 promoter activity was increased 2.8-fold compared with untreated control. Therefore IFN-gamma stimulates the stromelysin-1 promoter activity, resulting in transcriptional enhancement of gene expression. Transforming growth factor-beta (TGF-beta) showed the antagonistic action to the effects of IFN-gamma in cultured dermal fibroblasts. Furthermore, gel mobility shift assays demonstrated enhanced AP-1 binding activities in nuclear extracts from cells incubated with IFN-gamma. These data suggest that IFN-gamma is an up-regulator and TGF-beta is a down regulator on the stromelysin-1 gene expression, respectively, and the AP-1 binding site may be necessary for gene response.
