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A role for matrix metalloproteinase-9 in pathogenesis of urogenital Chlamydia muridarum infection in mice
Authors:Muhammad T. Imtiaz   John T. Distelhorst   Justin H. Schripsema   Ira M. Sigar   John N. Kasimos   Shanon R. Lacy  Kyle H. Ramsey  
Affiliation:aDepartment of Microbiology and Immunology, Chicago College of Osteopathic Medicine, Midwestern University, 555 31st Street, Downers Grove, IL 60515, USA;bDepartment of Pathology, Chicago College of Osteopathic Medicine, Midwestern University, 555 31st Street, Downers Grove, IL 60515, USA;cDepartment of Pathology and Laboratory Medicine, Van Nuys Medical Science Building, Room 128, 635 Barnhill Drive, Indianapolis, IN 46202-5120, USA
Abstract:Matrix metalloproteinases (MMPs) are a family of host-derived enzymes involved in the turnover of extracellular matrix (ECM) molecules and the processing of cytokines, chemokines and growth factors. We have previously reported that global inhibition of MMP in Chlamydia muridarum urogenital tract infection of susceptible strains of female mice impeded ascension of C. muridarum into the upper genital tract, blunted acute inflammatory responses and reduced the rate of formation of chronic disease. Because we have also observed that MMP-9 (also known as gelatinase B) is expressed in relatively large quantities in susceptible strains of mice in response to infection during acute phases of infection, we explored this further in a more selected fashion. We infected MMP-9 gene knockout mice and wild type controls intravaginally with C. muridarum. Both groups of mice had similar isolation rates from the lower urogenital tract but the absence of MMP-9 resulted in a slightly lower isolation rate in the upper genital tract, blunted acute inflammatory indices in the affected tissues and a reduced rate of formation of hydrosalpinx–a surrogate marker of infertility. These results imply that MMP-9 is involved in pathogenesis of chlamydial infection in this model possibly by amplifying inflammatory responses.
Keywords:Chlamydia   Matrix metalloproteinase-9   Mice   Inflammation
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