Human gingival glycosaminoglycans in cyclosporin-induced overgrowth

Glycosaminoglycans in normal and cyclosporin‐induced gingival overgrowth were extracted by papain digestion and purified by Mono Q‐FPLC chromatography. The purified glycosaminoglycans were analyzed by agarose gel electrophoresis and by the pattern of degradation products formed by chondroitin lyases...

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Published in:Journal of periodontal research Vol. 35; no. 3; pp. 158 - 164
Main Authors: Rocha, Lia A. G., Martins, Rita C. L., Werneck, Claudio C., Feres-Filho, Eduardo J., Silva, Luiz-Claudio F.
Format: Journal Article
Language:English
Published: Copenhagen Munksgaard International Publishers 01-06-2000
Blackwell
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Summary:Glycosaminoglycans in normal and cyclosporin‐induced gingival overgrowth were extracted by papain digestion and purified by Mono Q‐FPLC chromatography. The purified glycosaminoglycans were analyzed by agarose gel electrophoresis and by the pattern of degradation products formed by chondroitin lyases on HPLC chromatography. Our results on the glycosaminoglycan composition showed presence of chondroitin 4‐ and 6‐sulfate, dermatan sulfate, heparan sulfate and hyaluronic acid in both normal gingiva and cyclosporin‐induced gingival overgrowth. The total and relative amounts of glycosaminoglycans were similar between normal and overgrown gingiva. This suggests that the glycosaminoglycan composition is not changed in cyclosporin‐induced gingival overgrowth. Our present biochemical results conflict with histochemical and biosynthetic data previously reported by other groups. Those studies suggested that the affected tissues contained higher levels of glycosaminoglycans and that cyclosporin induced comparably high levels of these compounds in in vitro cultures of gingival fibroblasts. Therefore, these discrepant results suggest that a cyclosporin‐induced increase on gingival glycosaminoglycans still remains an open question. The implications of these conflicting results are discussed.
Bibliography:istex:A6806587E315B06D537A8E615DA335F4AD011334
ark:/67375/WNG-Z81DVKJC-4
ArticleID:pr90009
ISSN:0022-3484
1600-0765
DOI:10.1034/j.1600-0765.2000.035003158.x