Granzyme B promotes matrix metalloproteinase‐1 (MMP‐1) release from gingival fibroblasts in a PAR1‐ and Erk1/2‐dependent manner: A novel role in periodontal inflammation

Author:

Ben‐Eltriki Mohamed12,Ahmadi Amir Reza12,Nakao Yuya12,Golla Kalyan12,Lakschevitz Flavia2,Häkkinen Lari2,Granville David J.3,Kim Hugh124

Affiliation:

1. Centre for Blood Research University of British Columbia Vancouver British Columbia Canada

2. Department of Oral Biological and Medical Sciences University of British Columbia Vancouver British Columbia Canada

3. ICORD Centre and Department of Pathology and Laboratory Medicine, Vancouver Coastal Health Research Institute University of British Columbia Vancouver British Columbia Canada

4. Department of Biochemistry and Molecular Biology University of British Columbia Vancouver British Columbia Canada

Abstract

AbstractObjectiveTo gain insights into how proteases signal to connective tissues cells in the periodontium.BackgroundThe connective tissue degradation observed in periodontitis is largely due to matrix metalloproteinase (MMP) release by gingival fibroblasts. Granzyme B (GzmB) is a serine protease whose role in periodontitis is undefined.MethodsHuman gingival crevicular fluid (GCF) samples were obtained from sites with periodontal disease and healthy control sites. GzmB was quantified in the GCF ([GzmB]GCF) by ELISA. Gingival fibroblasts (GF) were cultured in the presence or absence of recombinant GzmB. Culture supernatants were analyzed by ELISA to quantify GzmB‐induced release of interstitial collagenase (MMP‐1). In some experiments, cells were pre‐treated with the inhibitor PD98059 to block MEK/ERK signaling. The protease‐activated receptor‐1 (PAR‐1) was blocked with ATAP‐2 neutralizing antibody prior to GzmB stimulation. Systemic MMP‐1 levels were measured in plasma from wild‐type (WT) and granzyme‐B‐knockout (GzmB−/−) mice.ResultsThe [GzmB]GCF in human samples was ~4–5 fold higher at sites of periodontal disease (gingivitis/periodontitis) compared to healthy control sites, suggesting an association between GzmB and localized matrix degradation. GzmB induced a ~4–5‐fold increase in MMP‐1 secretion by cultured fibroblasts. GzmB induced phosphorylation of Erk1/2, which was abrogated by PD98059. GzmB‐induced upregulation of MMP‐1 secretion was also reduced by PD98059. Blockade of PAR‐1 function by ATAP‐2 abrogated the increase in MMP‐1 secretion by GF. Circulating MMP‐1 was similar in WT and GzmB−/− mice, suggesting that GzmB's effects on MMP‐1 release are not reflected systemically.ConclusionThese data point to a novel GzmB‐driven signaling pathway in fibroblasts in which MMP‐1 secretion is upregulated in a PAR1‐ and Erk1/2‐dependent manner.

Funder

Canadian Institutes of Health Research

Michael Smith Foundation for Health Research

Publisher

Wiley

Subject

Periodontics

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