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MMP-25 Metalloprotease Regulates Innate Immune Response through NF-κB Signaling.
- Source :
-
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2016 Jul 01; Vol. 197 (1), pp. 296-302. Date of Electronic Publication: 2016 Jun 03. - Publication Year :
- 2016
-
Abstract
- Matrix metalloproteases (MMPs) regulate innate immunity acting over proinflammatory cytokines, chemokines, and other immune-related proteins. MMP-25 (membrane-type 6-MMP) is a membrane-bound enzyme predominantly expressed in leukocytes whose biological function has remained largely unknown. We have generated Mmp25-deficient mice to elucidate the in vivo function of this protease. These mutant mice are viable and fertile and do not show any spontaneous phenotype. However, Mmp25-null mice exhibit a defective innate immune response characterized by low sensitivity to bacterial LPS, hypergammaglobulinemia, and reduced secretion of proinflammatory molecules. Moreover, these immune defects can be tracked to a defective NF-κB activation observed in Mmp25-deficient leukocytes. Globally, our findings provide new mechanistic insights into innate immunity through the activity of MMP-25, suggesting that this proteinase could be a potential therapeutic target for immune-related diseases.<br /> (Copyright © 2016 by The American Association of Immunologists, Inc.)
- Subjects :
- Animals
Cells, Cultured
Cytokines metabolism
GPI-Linked Proteins genetics
GPI-Linked Proteins metabolism
Immunity, Innate genetics
Inflammation Mediators metabolism
Lipopolysaccharides immunology
Matrix Metalloproteinases, Membrane-Associated genetics
Mice
Mice, Inbred C57BL
Mice, Knockout
NF-kappa B metabolism
Protein Binding
Signal Transduction
Hypergammaglobulinemia immunology
Leukocytes immunology
Matrix Metalloproteinases, Membrane-Associated metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1550-6606
- Volume :
- 197
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of immunology (Baltimore, Md. : 1950)
- Publication Type :
- Academic Journal
- Accession number :
- 27259858
- Full Text :
- https://doi.org/10.4049/jimmunol.1600094