Literature DB >> 9777595

Dissolution of type I collagen fibrils by gingival fibroblasts isolated from patients of various periodontitis categories.

A Havemose-Poulsen1, P Holmstrup, K Stoltze, H Birkedal-Hansen.   

Abstract

The classification of periodontitis in various disease categories, including juvenile periodontitis, rapidly progressive adult periodontitis and slowly progressive adult periodontitis is based mainly on differences in disease progression and age group susceptibility. Because dissolution of collagen fibers is an integral part of periodontal attachment loss, we investigated whether the clinical differences among these periodontitis/control groups are reflected in the collagen-degrading activity of gingival fibroblasts isolated from affected tissues. All fibroblast strains isolated from the 4 groups (n = 48) displayed cell-associated collagenolytic activity when seeded in contact with a reconstituted film of type I collagen fibrils. Cells from the control group (n = 14) dissolved the collagen fibril film twice as fast as those from each of the 3 disease groups (juvenile periodontitis (n = 13), rapidly progressive adult periodontitis (n = 7), and slowly progressive adult periodontitis (n = 14)). Both interleukin-1 beta and phorbolester accelerated the rate of dissolution 2-4-fold, but even after cytokine or phorbolester stimulation control cells were still considerably more effective in dissolving the collagen fibrils than cells from the disease groups. The observation made in this study, that dissolution of collagen fibrils by gingival fibroblasts from periodontally diseased individuals is significantly slower than by cells from healthy control subjects, challenges disease paradigms based on a direct relationship between collagenolytic potential and disease activity.

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Year:  1998        PMID: 9777595     DOI: 10.1111/j.1600-0765.1998.tb02201.x

Source DB:  PubMed          Journal:  J Periodontal Res        ISSN: 0022-3484            Impact factor:   4.419


  5 in total

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Journal:  J Cell Biol       Date:  2004-11-22       Impact factor: 10.539

4.  Matrix metalloproteinases (MMPs) regulate fibrin-invasive activity via MT1-MMP-dependent and -independent processes.

Authors:  Kevin B Hotary; Ikuo Yana; Farideh Sabeh; Xiao-Yan Li; Kenn Holmbeck; Henning Birkedal-Hansen; Edward D Allen; Nobuaki Hiraoka; Stephen J Weiss
Journal:  J Exp Med       Date:  2002-02-04       Impact factor: 14.307

5.  Uncovering mediators of collagen degradation in the tumor microenvironment.

Authors:  Marie-Louise Thorseth; Marco Carretta; Christina Jensen; Kasper Mølgaard; Henrik J Jürgensen; Lars H Engelholm; Niels Behrendt; Nicholas Willumsen; Daniel H Madsen
Journal:  Matrix Biol Plus       Date:  2022-01-28
  5 in total

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