Journal article
Porphyromonas gingivalis-derived RgpA-Kgp complex activates the macrophage urokinase plasminogen activator system: Implications for periodontitis
AJ Fleetwood, NM O'Brien-Simpson, PD Veith, RS Lam, A Achuthan, AD Cook, W Singleton, IK Lund, EC Reynolds, JA Hamilton
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2015
Open access
Abstract
Urokinase plasminogen activator (uPA) converts plasminogen to plasmin, resulting in a proteolytic cascade that has been implicated in tissue destruction during inflammation. Periodontitis is a highly prevalent chronic inflammatory disease characterized by destruction of the tissue and bone that support the teeth. We demonstrate that stimulation of macrophages with the arginine- and lysine-specific cysteine protease complex (RgpA-Kgp complex), produced by the keystone pathogen Porphyromonas gingivalis, dramatically increased their ability to degrade matrix in a uPA-dependent manner. We show that the RgpA-Kgp complex cleaves the inactive zymogens, pro-uPA (at consensus sites Lys158-Ile159 and ..
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Funding Acknowledgements
This work was supported by grants from the National Health and Medical Research Council of Australia (to J. A. H.). The authors declare that they have no conflicts of interest with the contents of this article.