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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 199 (1963), S. 604-605 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The biological activity of pigment I has now been examined. The pigment used was extracted from the fermentation medium with liquid phenol as described previously1. It was purified by paper electrophoresis in 1ST acetic acid containing 0-01 per cent potassium cyanide followed by paper ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    BBA Section Nucleic Acids And Protein Synthesis 145 (1967), S. 214-217 
    ISSN: 0005-2787
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Munksgaard International Publishers
    Journal of clinical periodontology 31 (2004), S. 0 
    ISSN: 1600-051X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Limited attention has been given to the role mast cells may play in periodontal diseases.〈section xml:id="abs1-3"〉〈title type="main"〉Background: Mast cells are indeed found abundantly below and within several types of mucosal epithelia. On the basis of their proteinase content, mast cells are divided into connective tissue (CT) and mucosal phenotypes. The CT phenotype contains both tryptase and chymase (MCTC), while the mucosal phenotype contains only tryptase (MCT). The in vivo significance of different mast cell phenotypes has not yet been fully established. Mast cells are able to phagocytose, process and present antigens as effectively as macrophages.〈section xml:id="abs1-4"〉〈title type="main"〉Results: Recently mast cells were found in high numbers in chronically inflamed gingival tissue taken from patients with chronic marginal periodontitis (CMP). The number of mast cells was found to be even higher in HIV+ patients with CMP. Furthermore, mast cells also express strongly matrix metalloproteinases (MMPs), which are key enzymes in degradation of gingival extracellular matrix. Mast cells may release preformed cytokines directing local innate and adaptive immune responses. The present review will focus on possible roles for mast cells in periodontal diseases.〈section xml:id="abs1-5"〉〈title type="main"〉Conclusions: We certainly feel that this is a key cell in inflamed periodontal tissue and its role in periodontitis needs to be revisited.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Actinobacillus actinomycetemcomitans (A. actinomycetemcomitans) is supposed to be an important etiological agent in localized juvenile periodontitis (LJP). We have studied the effect of lipopolysaccharide (LPS) extracted from these periodontopathogenic bacteria on synthesis of the proinflammatory cytokities, interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and the anti-inflammatory cytokine IL-1 receptor antagonist (IL-lra) in human whole blood. LPS from A. actinomycetemcomitans in concentrations ≥ 1 ng/ml induced a significant production of all these proinflammatory cytokines, whereas LPS from Escherichia coli (E. coli), strain 026:B6 had to be added in concentrations ≥1 μg/ml to obtain a similar effect. Similarly, LPS from A. actinomycetemcomitans≥0.1 ng/ml resulted in production of IL-1ra, while LPS from E. coli 026:B6 had to be added at ≥10 ng/ml to obtain similar effects. It has been suggested that the ratio between production of proinflammatory and anti-inflammatory cytokines may influence the outcome of periodontal diseases. Other in vitro and in vivo studies have, however, indicated that very large excesses (100-1000 times) of IL-1ra compared to IL-1β are required to shift the IL-1ra:IL-1β ratio in favor of an inhibition of IL-1 bioactivity. In our ex vivo system, we found that stimulation with extremely low doses of A. actinomycetemcomitans LPS (0.1-1 ng/ml) resulted in IL-1ra production solely, without concomitant production of IL-1β, the excess of IL-1ra over IL-1β peaking at 1 ng/ml, which accordingly should suggest that LPS from A. actinomycetemcomitans primarily has proinflammatory effects.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 18 (1983), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The in vitro lymphocyte blastogenic responses of renal allograft recipients treated with immunosuppressive agents were compared with those of systemically healthy subjects with varying degrees of periodontal disease. The healthy subjects were divided into three groups; Group I showed no bleeding gingival units on gentle probing, Group II comprised persons with gingivitis, while Group III consisted of those with periodontitis. The target group (IS) comprised 11 renal allograft recipients maintained on an azathioprine and corticosteroid regimen. Two other such patients (Group CY) treated with cyclophosphamide and corticosteroids were also evaluated. Total and differential peripheral blood leukocyte counts from the IS group gave mean values within normal ranges. The mononuclear cells from peripheral blood were cultured for five days in a medium supplemented with foetal bovine serum. Triplicate cultures were stimulated with phytohemagglutinin and pokeweed mitogen. The responses of the IS patients and the systemically healthy subjects were not significantly different, whereas cells from the patients treated with cyclophosphamide showed impaired proliferative activity. When cultures were stimulated with a sonicate of dental plaque (DP), cells from the Groups II and III showed a statistically significant higher 3H-thymidine uptake than did those from the Groups I and IS (p〈0.05). The difference between the latter two groups was not statistically significant. The weak blastogenic responses of IS cells to DP antigens may be part of the explanation for the mild gingivitis observed in these patients.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Munksgaard International Publishers
    Journal of periodontal research 38 (2003), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background:  Mast cells are a prominent cell type in the gingival infiltrate in periodontitis. In this study we examined the expression by gingival mast cells of matrix metalloproteinases, MMP-1, MMP-2, MMP-8 and the tissue inhibitors of metalloproteinases, TIMP-1 and TIMP-2.Methods:  Gingival specimens from 12 human immunodeficiency virus-negative (HIV–) and 15 HIV-positive (HIV+) patients with chronic marginal periodontitis (CMP), and from 10 HIV– and four HIV+ controls with clinically healthy gingiva (HG) were examined after double immunofluorescence staining for mast cell tryptase, combined with antibodies for MMP-1, MMP-2, MMP-8 or their inhibitors TIMP-1 and TIMP-2.Results:  In the HIV+CMP, HIV+HG and HIV–CMP groups, all mast cells expressed MMP-1 and MMP-8, whereas a smaller proportion (40–60%) in the HIV–HG controls displayed such staining. The former groups also displayed a significantly higher proportion (39–64%) of mast cells expressing MMP-2 as compared with the HIV–HG group (21–31%). All groups displayed similar proportions of TIMP-1 expressing mast cells (86–100%), whereas significantly increased proportions of TIMP-2+ mast cells were seen in the HIV+CMP, HIV+HG and HIV–CMP groups (18–25%) as compared with the HIV–HG group (8–13%). Mast cells were the cell type that most prominently expressed MMP-1 and MMP-8. MMP-2 expression was also strong in mast cells, but was also similarly expressed in other cell types.Conclusion:  The chronically inflamed periodontal lesions in the present study appeared with little evidence of mast cell degranulation. The results show, however, that mast cells in inflamed gingiva have the potential to degrade extracellular matrix if appropriately triggered.
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