Expression of cathepsins B, D and L in mouse corneas infected withPseudomonas aeruginosa
Open Access
- 15 December 2001
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 268 (24) , 6408-6416
- https://doi.org/10.1046/j.0014-2956.2001.02607.x
Abstract
C57BL/6J naïve and immunized mice were intracorneally infected withPseudomonas aeruginosa. Semi‐quantitative RT‐PCR was performed to detect cathepsin gene expression and the results were further confirmed by immunoblot analysis. The enzymatic activities of cathepsins B, D and L were measured by peptidase assays. Immunohistochemical staining was carried out to localize the expression of the cathepsins. Cathepsins B, D and L were detected in the normal cornea by RT‐PCR. A peptidase assay revealed activities of all three cathepsins under normal physiological conditions. In naïve mice, enzymatic activities of cathepsins B, D and L were all significantly enhanced when the corneas were infected withP. aeruginosaand the peak of the induction appeared around day 6 postinfection. Immunoblot analysis showed increased expression of cathepsins B, D and L. The infected corneal samples from immunized mice exhibited much lower induction of enzymatic activities compared to those from naïve mice. Immunohistochemistry showed that the expression of cathepsins in the normal cornea was restricted to the epithelial tissue while the induced expression of cathepsins was predominantly in the substantia propria. Our data revealed up‐regulated enzymatic activities of cathepsins B, D and L in the naïve corneas infected withP. aeruginosa, which correlated well with the inflammatory response. Immunization of mice againstP. aeruginosaattenuated the inducing effect on cathepsin expression caused by infection. The time sequence for induction of cathepsin proteins and enzymatic activities suggests a mechanism of host proteolytic degradation of the extracellular matrix resulting in corneal destruction afterP. aeruginosainfection.Keywords
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