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Cysteine protease inhibitory activity and levels of salivary cystatins in whole saliva of periodontally diseased patients
Author(s) -
Baron A. C.,
Gansky S. A.,
Ryder M. I.,
Featherstone J. D. B.
Publication year - 1999
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.1999.tb02279.x
Subject(s) - cystatin , cystatin c , cysteine protease , saliva , protease , cathepsin , cysteine proteinase inhibitors , chemistry , porphyromonas gingivalis , proteases , cysteine , microbiology and biotechnology , antibacterial activity , pharmacology , biochemistry , periodontitis , biology , enzyme , bacteria , medicine , apoptosis , genetics , programmed cell death , renal function , caspase
The 3 human salivary cystatins S, SA and SN are multifunctional proteins that possess a cysteine protease inhibitory property, but their ability to act as such is very different (SN > SA ≫ S). One form, S, also appears to possess antibacterial properties towards the bacterium Porphyromonas gingivalis , often associated with periodontal diseases. In this study we measured the total cystatin inhibitory activity and the levels of each salivary cystatin in the whole saliva of 8 periodontally diseased patients and 2 groups of control subjects ( n = 6 and n = 10). The total cystatin inhibitory activity and the total salivary cystatin concentration in the periodontally diseased patients were found to be lower than the controls ( p ≤ 0.005). The concentration of S was depleted to levels that would not allow it to be an effective antibacterial agent, and the concentration of SA, although depleted in some cases, was still present at sufficient levels to allow it to act as an effective physiological inhibitor of cathepsin L. The concentration of cystatin SN was also depleted in the periodontally diseased patients, but was still present in sufficient quantities to act as an effective physiological cysteine protease inhibitor of cathepsins H and L. In comparison, the concentration of all 3 salivary cystatins in the control subjects were sufficient to enable these proteins to be both effective physiological cysteine protease inhibitors and antibacterial agents.