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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 31 (1996), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In previous studies it was noted that alkaline phosphatase (ALP) activity in periodontal ligament does not only seem to be related to cells but may also be associated with the extracellular matrix. In an attempt to clarify this we studied the distribution of the enzyme at the electron microscopic level. In addition, ALPactivity was assessed biochemically following extraction of the ligament with (i) agents dissolving the membrane or splitting the phosphatidylinositol anchor (Triton X-100 or phosphatidylinositol-phospholipase C, respectively), and (ii) a matrix-degrading enzyme cocktail (collagenase, hyaluronidase and elastase). Histochemical observations revealed (a) a heterogeneous distribution of ALP-activity, with highest activity adjacent to the alveolar bone and (b) two pools of activity; one bound to cells and one associated with the collagenous extracelluJar matrix. In line with this were the biochemical data indicating that approximately 10% of the enzyme activity was firmly bound to the extracellular matrix and 90% to plasma membranes. Isoelectric focusing did not reveal differences between the two fractions, both samples yielding a single broad band corresponding with an isoelectric point of about 4.4.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 17 (1982), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: During eruption of the mouse incisor part of the periodontal ligament moves along with the tooth in the occlusal direction and is degraded in the supra-alveolar region.In the present study stereologic analysis at the ultrastructural level has shown that significant reduction of the amount of extracellular collagen is confined to the most occlusal region of the ligament, just apically to the functional epithelium. In connection herewith a relatively high amount of homogeneous material of moderate electron density was found in the intercellular space, suggesting a process of extracellular collagen breakdown near the epithelium-connective tissue interface.With respect to the distribution of collagen phagocytosis by fibroblasts, it appeared that the volume density of cytoplasmic vacuoles containing collagen fibrils was considerably higher in the supra-alveolar region of the ligament than in its subcrestal part, particularly in the zone along the tooth surface. This phenomenon is interpreted as being indicative of increased phagocytic activity of fibroblasts leading to the detachment of the periodontal ligament from the cemeatum before it enters the region of final degradation near the apical termination of the junctional epithelium.In an attempt to identify the cells involved in the degradation of (fragments of) periodontal fibroblasts in the supra-alveolar region, periodontal ligament cells were labelled with tritiated thymidine at their site of origin. By means of both autoradiography and electron microscopy, it was shown that, following the arrival of Jabelled fibroblasts in the supra-alveolar region, at least part of the degradation of cellular constituents is accomplished via a process of heterophagocytosis among fibroblasts.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The capacity of the periodontal ligament to alter its structure and mass in response to mechanical loading has long been recognized. However, the mechanism by which periodontal cells can detect physical forces and respond to them is largely unknown. Besides transmission of forces via cell-matrix or cell-cell interactions, the strain-derived flow of interstitial fluid through the periodontal ligament may mechanically activate the periodontal cells, as well as ensure transport of cell signaling molecules, nutrients and waste products. Mechanosensory cells, such as endothelial and bone cells, are reported to respond to a flow of fluid with stimulated prostaglandin E2(PGE2) and nitric oxide production. Therefore, we examined the PGE2 and nitric oxide response of human periodontal ligament and gingival fibroblasts to pulsating fluid flow and assessed the expression of tissue non-specific alkaline phosphatase activity. Periodontal ligament and gingival fibroblasts were subjected to a pulsating fluid flow (0.7±0.02 Pa, 5 Hz) for 60 min. PGE2 and nitric oxide concentrations were determined in the conditioned medium after 5, 10, 30 and 60 min of flowing. After fluid flow the cells were cultured for another 60 min without mechanical stress. Periodontal ligament fibroblasts, but not gingival fibroblasts, responded to fluid flow with significantly elevated release of nitric oxide and decreased expression of tissue non-specific alkaline phosphatase activity. In both periodontal ligament and gingival fibroblasts, PGE2 production was significantly increased after 60 min of flowing. Periodontal ligament fibroblasts, but not gingival fibroblasts, produced significantly higher levels of PGE2 during the postflow culture period. We conclude that human periodontal ligament fibroblasts are more responsive to pulsating fluid flow than gingival fibroblasts. The similarity of the early nitric oxide and PGE2 responses to fluid flow in periodontal fibroblasts with bone cells and endothelial cells suggests that these three cell types possess a similar sensor system for fluid shear stress.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 31 (1996), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Alkaline phosphatase (ALP) has been suggested to play a role in acellular cementum formation and maintenance of periodontal attachment. In an attempt to determine whether changes in attachment level are associated with altered expression of ALP-activity in the periodontium we induced natural loss of attachment in rats by pinning the lower incisor to the jaw bone. Previous studies have shown that this procedure results in regressive changes in the marginal periodontium without any inflammatory response. Six months after blockage of eruption the attachment level on the experimental (right) side had shifted about 700 μ in the apical direction. On the control (left) side the apical termination of the junctional epithelium had remained stationary with respect to the alveolar crest. Our observations have shown that during the first few weeks of the experiment loss of attachment is accompanied by considerable reduction of ALP-activity in the supracrestal part of the periodontium. At later time intervals, however, no distinct relation was found between apical migration of junctional epithelium and loss of ALP-activity in the supracrestal region, indicating that the two phenomena are not directly related to each other. The domain of the ALP-positive fibroblasts in the supracrestal extension of the periodontal ligament decreased in size and was replaced by ALP-negative connective tissue cells probably coming from the outer gingival domain. Since at all time intervals a distinct demarcation could be observed between the ALP-positive and ALP-negative areas, we interpret our data as indicating that ligament and gingival cells do not mix.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 19 (1984), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The effects of the anti-microlubular drug colchicine on the eruption of the continuously growing mouse incisor and the structure of its periodontal ligament, which is thought to be responsible for generating the eruptive force were studied. It was observed that both the eruptive process and the microtubular apparatus in the cells of the ligament are affected by the drug in a dose-dependent fashion, thereby lending support to the view that eruption is related to the functioning of microtubules in periodontal ligament cells. Since colchicine did not seem to interfere with collagen degradation. as measured in terms of collagen phagocytosis by fibroblasts and loss of connective tissue attachment in the supra-alveolar region, the inhibition of eruption is not likely to be due to an increased resistance force in the periodontal ligament as a result of decreased collagen breakdown.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 15 (1980), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Quantitative evaluation of the distribution of intercellular junctions between fibroblasts in the incisor and molar periodontal ligament of the mouse indicated that structures resembling gap junctions are more frequent on the tooth side of this tissue than on the bone side. The difference was particularly evident for the ligament of the continuously erupting incisor. Here, the numerical density of gap junction-like structures was estimated to be approximately 20 per fibroblast in the connective tissue adjacent to the cementum and 4 per fibroblast in the tissue along the alveolar bone. With regard to the distribution of adhaerens-type junctions less variation was observed between the various zones of the incisor and molar ligament. For the incisor the average number of adhaerens-type junctions was calculated to be in the order of 30 junctions per cell in the tooth-related compartment and 20 junctions per cell in the alveolar compartment.Although in the molar intercellular junctions were observed throughout the entire width of the ligament, in the incisor they were confined to the two main connective tissue compartments, i.e. the one of the tooth side which moves with the erupting tooth in the direction of the oral cavity, and the one of the bone side which remains stationary with respect to the alveolar wall. In the transitional area between the two latter compartments junctions were very sparse. It is suggested that the distribution pattern of intercellular junctions between fibroblasts in mouse periodontal ligament reflects functional differences among the cells in the various regions of the tissue, differences that are possibly related to processes involving the movement of cells and the metabolism of collagen.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 16 (1981), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In this study we investigated the possible role of the junctional epithelium of the mouse incisor in the degradation of collagen fibers carried during eruption from the periodontal ligament into the gingiva. To eliminate the contribution of fibroblasts to collagen breakdown the periodontal ligament was frozen in the sub-crestal region by local application of liquid nitrogen. As a result of this treatment the fibroblasts were disrupted and, with ongoing eruption, the ligament was split into two separate sets of collagen fibers, one attached to the incisor and the other to the alveolar bone. The injured connective tissue in the tooth-related compartment continued to move in the occlusal direction and made contact with the intact gingiva. Following its arrival in the sub-epithelial region, the collagen fibers were not degraded but carried further towards the incisal edge, a process resulting in a forward shift of the level of connective tissue attachment. The degree to which this occurred was inversely proportional to the number of fibroblasts which had repopulated the connective tissue adjacent to the incisor. The data suggest that degradation of collagen and maintenance of connective tissue attachment in mouse incisor gingiva cannot solely be performed by cells of the junctional epithelium but require primarily the degradative activity of fibroblasts.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Munksgaard International Publishers
    Journal of periodontal research 37 (2002), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: We showed recently that human periodontal ligament (PDL) and gingival fibroblasts adhere and spread on enamel matrix protein (EMP) coatings (1). In the present study, we investigated whether this interaction can be attributed to integrin expression. Human PDL and gingival fibroblasts were cultured for periods up to 24 h on EMP coatings, in the presence of synthetic RGD-containing peptide or an antibody against the β1 integrin subunit. The cells were first cultured for 24 h under serum-free conditions and then cultured on EMP coatings for 48 h. Integrin expression levels were assessed by flow cytometry analysis. It was found that attachment and spreading on EMP was inhibited by the synthetic RGD-containing peptide, but not by a synthetic RGE-peptide. Both PDL and gingival fibroblasts showed expression of the integrin subunits, α2, α5, β1, and the integrin, αvβ3. Incubation with an antibody against the β1 subunit significantly inhibited the attachment and spreading of PDL and gingival fibroblasts on EMP coatings. We conclude that integrins are involved in the interaction of PDL and gingival fibroblasts with EMP.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 178 (1991), S. 178-184 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Biology International Reports 11 (1987), S. 496 
    ISSN: 0309-1651
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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