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Zinc-binding protein-89 (ZBP-89) cooperates with NF-κB to regulate expression of matrix metalloproteinases (MMPs) in
Ruth C Borghaei1, Grzegorz Gorski1, Sara Seutter1
1Department of Biomedical Sciences, Philadelphia College of Osteopathic Medicine, 4170 City Ave., Philadelphia, PA 19131, USA.
Abstract:
Matrix metalloproteinases (MMPs) have both protective and pathological roles in inflammation, and transcriptional mechanisms are important in regulating physiological levels to maintain health. Zinc-binding protein-89 (ZBP-89) is a transcription factor with roles in regulating vital cellular processes, acting through complex interactions with other proteins to ensure appropriate expression of tightly regulated genes. ZBP-89 binds the MMP-3 promoter at a polymorphic (5A/6A) site along with NF-κB. This polymorphism affects MMP-3 protein levels in tissues. In disease association studies, both over- and under-expression has negative consequences to health, and this promoter element is important in maintaining balanced expression. There is evidence that effects of the polymorphism vary under different conditions, but the role of ZBP-89 in these differences is not known. ZBP-89 was stably knocked-down in MG-63 osteosarcoma cells in order to study its role in regulation of MMP-3 expression in response to cytokines, and evaluate the functionality of a putative binding site in the MMP-1 promoter. Results show ZBP-89 is needed for maximal induction of both genes by IL-1β and TNFα. Binding of both ZBP-89 and NF-κB to both promoters was decreased in the knock-down cells under basal and TNF-induced conditions, and protein interactions between ZBP-89 and NF-κB were suggested. These data provide the first evidence of a role for ZBP-89 in regulation of MMP-1 expression, and suggest the possibility of a larger role for ZBP-89 in inflammation through interactions with NF-κB.
Insights
Zinc-binding protein-89 (ZBP-89) is crucial for regulating matrix metalloproteinase (MMP) gene expression, particularly MMP-3 and MMP-1, in response to inflammatory signals. This transcription factor interacts with NF-κB, influencing gene induction and potentially impacting inflammatory diseases.
Area of Science:
- Molecular Biology
- Cellular Biology
- Genetics
Background:
- Matrix metalloproteinases (MMPs) play dual roles in inflammation, with transcriptional regulation vital for maintaining health.
- Zinc-binding protein-89 (ZBP-89) is a transcription factor involved in regulating gene expression through protein interactions.
- ZBP-89 binds the MMP-3 promoter, and its interaction with NF-κB at a polymorphic site influences MMP-3 levels.
Purpose of the Study:
- To investigate the role of ZBP-89 in the regulation of MMP-3 and MMP-1 expression.
- To determine ZBP-89's function in cytokine-induced gene expression.
- To explore ZBP-89's interaction with NF-κB in regulating MMP promoters.
Main Methods:
- Stable knockdown of ZBP-89 in MG-63 osteosarcoma cells.
- Analysis of MMP-3 and MMP-1 gene expression in response to IL-1β and TNFα.
- Assessment of ZBP-89 and NF-κB binding to MMP promoters via chromatin immunoprecipitation assays.
Main Results:
- ZBP-89 knockdown significantly reduced the induction of MMP-3 and MMP-1 by IL-1β and TNFα.
- Binding of both ZBP-89 and NF-κB to the MMP-3 and MMP-1 promoters was diminished in ZBP-89 knockdown cells.
- Evidence suggests protein-protein interactions between ZBP-89 and NF-κB.
Conclusions:
- ZBP-89 is essential for the maximal induction of MMP-3 and MMP-1 by inflammatory cytokines.
- ZBP-89 interacts with NF-κB, suggesting a collaborative role in regulating MMP gene expression.
- This study reveals a novel role for ZBP-89 in MMP-1 regulation and highlights its broader potential involvement in inflammation.
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