Epigenetics and rheumatoid arthritis: the role of SENP1 in the regulation of MMP-1 expression.
The aggressive phenotype of RA synovial fibroblasts (RASF) is characterised by the increased expression of matrix metalloproteinase (MMP)-1 as well as the small ubiquitin like modifier (SUMO)-1 and decreased expression of SUMO-specific protease SENP1. Since we showed an increased activity of acetyltransferases in this autoimmune disease, we wanted to analyze ... whether this affects the expression of MMP-1 and can be reversed by the reconstitution of SENP1. In RASF, the acetylation of histone H4 was significantly increased in the distal region of the MMP-1 promoter by 274 +/- 36% compared to OASF. Most interestingly, overexpression of SENP1 in RASF decreased acetylation specifically in this region by 51 +/- 0.5% and globally by 73 +/- 11%. Furthermore, the overexpression of SENP1 resulted in a downregulation of MMP-1 at both the mRNA (58 +/- 7%) and protein levels (28 +/- 6%), significantly reduced the invasiveness of RASF (from 34 +/- 9% to 2 +/- 2%) and led to an accumulation of histone deacetylase 4 (HDAC4) on the MMP-1 promoter (197 +/- 36%). Interestingly, SENP1 failed to modulate the expression of MMP-1 in the cells silenced for HDAC4. This is the first study linking the SUMOylation pathway and the production of MMP-1 to an epigenetic control mechanism mediated through histone acetylation which has a functional consequence for the invasiveness of RASF.
Mesh Terms:
Adenosine Triphosphatases, Antibodies, Archaeal Proteins, Chromatography, Gel, Chromosome Pairing, Cross Reactions, Cross-Linking Reagents, DNA-Binding Proteins, Escherichia coli, Fluorescence, Immunoprecipitation, Models, Biological, Protein Binding, Protein Isoforms, Protein Multimerization, Recombination, Genetic, Sulfolobus solfataricus, Temperature
Adenosine Triphosphatases, Antibodies, Archaeal Proteins, Chromatography, Gel, Chromosome Pairing, Cross Reactions, Cross-Linking Reagents, DNA-Binding Proteins, Escherichia coli, Fluorescence, Immunoprecipitation, Models, Biological, Protein Binding, Protein Isoforms, Protein Multimerization, Recombination, Genetic, Sulfolobus solfataricus, Temperature
J. Autoimmun.
Date: Aug. 01, 2010
PubMed ID: 20079608
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