| Literature DB >> 27259858 |
Clara Soria-Valles1, Ana Gutiérrez-Fernández1, Fernando G Osorio1, Dido Carrero1, Adolfo A Ferrando2, Enrique Colado3, M Soledad Fernández-García4, Elena Bonzon-Kulichenko5, Jesús Vázquez5, Antonio Fueyo6, Carlos López-Otín7.
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.Entities:
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Year: 2016 PMID: 27259858 DOI: 10.4049/jimmunol.1600094
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422