Regulation of matrixmetalloproteinase-3 and matrixmetalloproteinase-13 by SUMO-2/3 through the transcription factor NF-κB

Autor: Svetlana Frank, Marvin A Peters, Corinna Wehmeyer, Simon Strietholt, Christina Koers-Wunrau, Jessica Bertrand, Marianne Heitzmann, Anja Hillmann, Joanna Sherwood, Christine Seyfert, Steffen Gay, Thomas Pap
Přispěvatelé: University of Zurich, Frank, Svetlana
Rok vydání: 2013
Předmět:
Small interfering RNA
2745 Rheumatology
Immunology
Mice
Transgenic

610 Medicine & health
Biology
environment and public health
General Biochemistry
Genetics and Molecular Biology

Arthritis
Rheumatoid

Mice
chemistry.chemical_compound
Rheumatology
Western blot
1300 General Biochemistry
Genetics and Molecular Biology

Matrix Metalloproteinase 13
Osteoarthritis
medicine
Animals
Humans
Immunology and Allergy
Ubiquitins
Transcription factor
2403 Immunology
Gene knockdown
medicine.diagnostic_test
Tumor Necrosis Factor-alpha
Synovial Membrane
NF-kappa B
10051 Rheumatology Clinic and Institute of Physical Medicine
Wild type
Interleukin
NF-κB
Fibroblasts
Molecular biology
chemistry
Small Ubiquitin-Related Modifier Proteins
2723 Immunology and Allergy
Matrix Metalloproteinase 3
Tumor necrosis factor alpha
Signal Transduction
Zdroj: Annals of the Rheumatic Diseases. 72:1874-1881
ISSN: 1468-2060
0003-4967
Popis: Objective Based on previous data that have linked the small ubiquitin-like modifier-1 (SUMO-1) to the pathogenesis of rheumatoid arthritis (RA), we have investigated the expression of the highly homologous SUMO family members SUMO-2/3 in human RA and in the human tumour necrosis factor α transgenic (hTNFtg) mouse model of RA and studied their role in regulating disease specific matrixmetalloproteinases (MMPs). Methods Synovial tissue was obtained from RA and osteoarthritis (OA) patients and used for histological analyses as well as for the isolation of synovial fibroblasts (SFs). The expression of SUMO-2/3 in RA and OA patients as well as in hTNFtg and wild type mice was studied by PCR, western blot and immunostaining. SUMO-2/3 was knocked down using small interfering RNA in SFs, and TNF-α induced MMP production was determined by ELISA. Activation of nuclear factor-κB (NF-κB) was determined by a luciferase activity assay and a transcription factor assay in the presence of the NF-κB inhibitor BAY 11-7082. Results Expression of SUMO-2 and to a lesser extent of SUMO-3 was higher in RA tissues and RASFs compared with OA controls. Similarly, there was increased expression of SUMO-2 in the synovium and in SFs of hTNFtg mice compared with wild type animals. In vitro, the expression of SUMO-2 but not of SUMO-3 was induced by TNF-α. The knockdown of SUMO-2/3 significantly increased the TNF-α and interleukin (IL)-1β induced expression of MMP-3 and MMP-13, accompanied by increased NF-κB activity. Induction of MMP-3 and MMP-13 was inhibited by blockade of the NF-κB pathway. TNF-α and IL-1β mediated MMP-1 expression was not regulated by SUMO-2/3. Conclusions Collectively, we show that despite their high homology, SUMO-2/3 are differentially regulated by TNF-α and selectively control TNF-α mediated MMP expression via the NF-κB pathway. Therefore, we hypothesise that SUMO-2 contributes to the specific activation of RASF.
Databáze: OpenAIRE