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  • 1
    ISSN: 1468-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Computed morphometric analysis of elastic skin fibres in patients with cutis laxa, anetoderma, Williams–Beuren syndrome, pseudoxanthoma elasticum (PXE), and Buschke–Ollendorff syndrome, all clinically ascertained, was performed and compared with data obtained from healthy individuals of the same age. The diameters, area fractions (AA%) and volume fractions (VV%) occupied by pre-elastic fibres and dermal elastic fibres were determined. Irrespective of age the diameter of dermal elastic fibres followed a Gaussian distribution for all groups studied. These diameters were taken into consideration for VV% determinations. Compared with data from skin of healthy subjects of similar age range, VV% of pre-elastic fibres was significantly decreased in patients with cutis laxa, anetoderma, Williams–Beuren syndrome, and PXE and undetectable in Buschke–Ollendorff patients. VV% of dermal elastic fibres was four- to fivefold increased in Buschke–Ollendorff syndrome, two- to threefold increased in PXE skin, four- to fivefold decreased in cutis laxa and anetoderma skin and about twofold decreased in Williams–Beuren skin. The diameter of oxytalan fibres was decreased in anetoderma and Williams–Beuren syndrome while oxytalan fibre diameter was unchanged in PXE and cutis laxa. The diameter of dermal elastic fibres was increased in PXE and Buschke–Ollendorff syndrome, but was decreased in anetoderma and Williams–Beuren syndrome and unchanged in cutis laxa. We demonstrated that cutis laxa, anetoderma, Williams–Beuren syndrome, PXE, and Buschke–Ollendorff syndrome could be easily differentiated by morphometric analysis of elastic skin fibres. Thus we propose that morphometric analyses together with skin biopsies are a valuable tool for distinguishing between inherited and/or acquired skin diseases known to display alterations of elastic fibres.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cell Biology International 18 (1994), S. 111-118 
    ISSN: 1065-6995
    Keywords: [abr] human skin fibroblasts = HSF ; [abr] insoluble elastin = iE ; [abr] recombinant TIMP"1 = Ree TIMP"1 ; [abr] succinyl-alanine-alanine-alanine-p-nitroanilide = Sue (Ala)"3 NA ; [abr] κ-elastin = κE ; fibroblasts, elastase activity, gelatinase(s), elastin-derived peptides
    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 : Blackwell Publishing Ltd
    British journal of dermatology 137 (1997), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The extent of alterations to the elastic fibre network in lesional skin areas of three patients with anetoderma was assessed by quantitative image analysis of tissue sections and compared with morphometric parameters from unaffected sites of the same individuals. In the anetodermic skins pre-elastic fibres were undetectable or extremely rare; the volume fraction (Vv%) occupied by these pre-elastic fibres was 0–0·3%, while in unaffected skins the Vv% occupied by pre-elastic fibres was 0·5–0·8%. A nearly complete absence of dermal elastic fibres in lesional skins from the three patients was evidenced (Vv%= 0·2–0·3%).Organ cultures were performed using explants from skin with or without anetodermic lesions to quantify the expressions of elastase-type proteinases. All tissues from anetodermic lesions expressed proforms of gelatinases A and B and the activated form of gelatinase A: their levels increased with the culture time. In comparison, enzymatic activities on oligopeptide substrates specific for leucocyte elastase and fibroblast plasma membrane-associated metalloelastase were not detected in the conditioned media of any explants at any time of culture from 1 to 5 days. Increased production of progelatinases A and B and activation of progelatinase A could be mainly responsible for the degradation of skin elastic fibres demonstrated in anetodermic skins.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The morphometric parameters of mid-dermal elastic fibres from the skin of four patients with Marfan syndrome, four patients with Ehlers-Danlos syndrome type IV (EDS IV), and two patients with pseudoxanthoma elasticum (PXE) were determined, and compared with those of healthy individuals of a similar age range.The volume fraction occupied by elastic fibres was significantly reduced in Marfan patients compared with normal controls, and this was independent of age. In contrast, it was significantly increased in PXE patients, whereas the volume fraction occupied by skin elastic fibres varied within the EDS IV group.Dermal elastic fibres from patients with Marfan syndrome. EDS IV and PXE are hydrolysed by human neutrophil elastase in a qualitatively and quantitatively different fashion from those from healthy individuals. Marfan syndrome and EDS IV dermal elastic fibres were found to be more resistant to hydrolysis by human neutrophil elastase, but PXE elastic fibres were hydrolysed at a rate similar to elastic fibres from control skin.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1600-0625
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract:  The aim of this work was to validate an image analysis method, based on cell nuclei form factor determination, for counting fibroblasts within human dermis. We first used reconstructed dermal equivalents in which fibroblasts can also be counted directly after lysis of the collagen matrix. We found a good correlation between the results of direct counting and those of image analysis from day 10 to day 28 of culture. When applied to young normal donors' skin biopsies fixed in Bouin's solution and embedded in paraffin, the image analysis method yielded mid-dermis fibroblast counts of between 2100 and 4100 per mm3 of fresh tissue. A nuclear form factor (FF) comprised between 0.35 and 0.84 was found to be a biologic marker of fibroblasts. This was confirmed after fibroblast discrimination from other cell types, which had rounder nuclei (FF ≥ 0.85) and were identified either by their location (e.g. endothelial cells) or by labeling with specific antibodies (e.g. lymphocytes and monocytes/macrophages). Similar results were obtained with seven healthy donors' skin biopsies that had been frozen in nitrogen liquid and cryostat-sectioned, showing that this counting method is independent of the histologic procedure. Finally, analysis of samples of hypertrophic scars from two patients revealed that fibroblast density in some parts of the dermis was more than twice the value found in other parts presenting a fibroblast density almost normal, showing that this cell counting method can also be used to assess fibroblast heterogeneity within a given tissue.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1436-3771
    Keywords: Key words Gingiva ; Skin ; Elastic fibers ; Collagen fibers ; Aging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The morphometric parameters of the human gingival elastic fiber network were determined by image analysis and compared with human skin elastic fibers in relation to age. Similarly, collagen fibers were also investigated in both tissues. In this study, 47 healthy patients, 10 – 75 years old were studied for gingiva and another 50 patients in the same age range were included for skin biopsies. Three groups were compared: group 1 from the age of 10 – 24 years, group 2 from 25 to 49 years, and group 3 from 50 to 75 years. The diameters of the oxytalan fibers were invariable in both tissues, whatever the age considered. On the other hand, the diameters of elastic fibers increased regularly with age in the gingiva (P〈0.01) and in the skin (P〈0.01) between each age group. The area fraction occupied by the oxytalan fibers decreased significantly in both tissues (P〈0.01) for the skin and (P〈0.001) for the gingiva. The area fraction occupied by the gingival elastic fibers remained constant with age while the skin elastic fibers increased significantly with age between groups 2 and 1 (P〈0.01) and between groups 3 and 2 (P〈0.001). In the mid-dermis and in the mid-gingiva, the diameters of the collagen fibers increased strongly with age, between groups 2 and 1 (P〈0.01) and between groups 3 and 2 (P〈0.001). The area fraction occupied by the collagen bundles increased regularly with age in the mid-gingival (P〈0.05 between each age group), while a significant decrease was observed in the mid-dermis from the age of 50 – 75 years (P〈0.05). The results obtained contribute to a better understanding of some modifications which dermis and gingiva undergo with aging and provide data to perfect diagnosis and therapy in odontology and dermatology.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 40 (1998), S. 164-169 
    ISSN: 0021-9304
    Keywords: gingiva ; collagen ; polysaccharides ; heparin ; dextran ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Gingival fibroblasts are particularly involved in the physiologic maintenance and repair of periodontium. During these processes, cell proliferation and synthesis of a collagen-rich gingival matrix should be controlled. A dextran derivative, namely, carboxy methyl dextran benzylamide sulfonate (CMDBS), considered to be a functional analog of heparin, was previously described to regulate proliferation of different types of cells and independently to modulate the expression of collagen biosynthesis. In this report, we demonstrate that CMDBS and heparin inhibited gingival fibroblast proliferation. We then analyzed collagen biosynthesis by measuring the incorporation of the radiolabeled [3H]proline precursor into collagen by postconfluent gingival fibroblasts. Our results showed CMDBS did not alter total collagen synthesis; it induced the preferential accumulation of newly synthesized collagen into the pericellular matrix; and it decreased the expression of type III collagen, particularly in the cell layer. Taken together, our results suggest that by inhibiting cell proliferation, CMDBS could induce the synthesis of an extracellular collagenous matrix which forms a network between gingival fibroblasts. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 40, 164-169, 1998.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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