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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 14 (1975), S. 3573-3580 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    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 purpose of the study was to characterize the noncollagenous acid-soluble proteins of gingiva and to determine their function. Gingival tissues of healthy adult dogs and those with spontaneously occurring advanced periodontitis were studied. The dental laminac from newborn puppies and skin of newborn and adult animals were also analyzed. Tissues were extracted with buffered salt at neutral pH followed by 0.5 M acetic acid. SDS-polyacrylamide gel electrophoresis revealed that salt extracts of all of the tissues contained collagens and several more rapidly migrating components; the latter cross-reacted with an antiserum to whole dog serum and were, therefore, derived from serum and tissue fluids. The acid extracts of normal gingiva contained a family of collagenase-resistant, pepsin-sensitive components ranging in size from about 32 kD to 75 kD. These components did not cross-react with the antiserum and appeared to be components of the connective tissues. They were partially purified by DEAE-cellulose chromarography and shown to be similar to the acidic structural glycoproteins of other connective tissues. These acid-soluble proteins were present in moderate to large amounts in extracts of healthy gingival tissues and in trace amounts in dental lamina. The amount in extracts of regenerated gingiva was much greater than in extracts of normal gingiva. Only traces were found in the extracts of gingivae from animals with spontaneous periodontitis. The data indicate that these proteins may be important structural components of the normal connective tissue matrix, and their loss during the early stages of periodontitis may be an important event in progressive tissue destruction.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 105 (1980), S. 503-512 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The effects of fresh human serum (FHS) and heat-inactivated human serum (HHS) on the DNA synthesis and proliferation of human diploid fibroblasts were assessed. FHS activated significantly more quiescent fibroblasts to undergo DNA synthesis and proliferation than did HHS. The stimulatory effect occurred consistently over a serum concentration range of 0.1-10%. Using bromodeoxyuridine selective killing techniques, it was shown that this FHS stimulatory effect was on a specific subpopulation of fibroblasts unresponsive to HHS. The involvement of the complement system, and specifically of C1, was shown by the inability of Clq-depleted FHS to support enhanced DNA synthesis whereas Clq-depleted serum reconstituted with purified Clq was effective. Purified Clq did not restore activity when added to heated serum, nor was it mitogenic when tested in basal medium without serum. The addition of purified Clq to fresh serum inhibited the enhancement of DNA synthesis, and at Clq concentrations of 4γ/ml and greater, the fresh serum effects were abrogated. Thus, it appears that binding of the assembled C1 complex to the fibroblast surface was required for FHS-mediated enhancement of fibroblast proliferation, with Clq subcomponent serving as the recognition site. The results from several experiments indicated that antibody was not required for the complement-dependent fibroblast activation. FHS was not cytotoxic, and autologous serum was as effective as allogeneic sera. A 20-fold molar excess of Fab' from pooled human IgG did not alter the FHS effects. FHS from which IgG was more than 99% depleted was still effective. These results suggested an antibody-independent role for complement in the activation of a subpopulation of human diploid fibroblasts.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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