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Morphometric Studies of Collagen and Fibrin Lattices Contracted by Human Gingival Fibroblasts; Comparison with Dermal FibroblastsCentre d'Etudes des Biomateriaux et Interfaces, EA 2068, IFR 53 Biomolecules, UFR d'Odontologie, 2, rue du General Koenig, 51100 Reims, France
Laboratoire de Biochimie et Biologie Moleculaire, UPRESA 6021 CNRS, IFR 53 Biomolecules, Faculte de Medecine, 51, rue Cognacq-Jay, 51095 Reims France
Laboratoire de Biochimie, Faculte de Chirurgie Dentaire, Universite Rene Descartes, 1, rue Maurice Arnoux, 92120 Montrouge, France
Laboratoire de Biochimie, Faculte de Chirurgie Dentaire, Universite Rene Descartes, 1, rue Maurice Arnoux, 92120 Montrouge, France
Laboratoire de Biochimie et Biologie Moleculaire, UPRESA 6021 CNRS, IFR 53 Biomolecules, Faculte de Medecine, 51, rue Cognacq-Jay, 51095 Reims France
Laboratoire de Biochimie et Biologie Moleculaire, UPRESA 6021 CNRS, IFR 53 Biomolecules, Faculte de Medecine, 51, rue Cognacq-Jay, 51095 Reims France
Centre d'Etudes des Biomateriaux et Interfaces, EA 2068, IFR 53 Biomolecules, UFR d'Odontologie, 2, rue du General Koenig, 51100 Reims, France Cell shape variations and substratum re-organization during contraction of floating collagen and fibrin lattices seeded with human gingival fibroblasts were determined by computerized image analysis of light and scanning electron microscopic images. Data were compared with those obtained with lattices populated with human dermal fibroblasts. The extent of collagen lattice contraction was similar with both cell types, resulting in a two-fold decrease in the area fractions occupied by collagen fibers. Fibroblasts exhibited a rounded shape (form factors equal to 0.8 and 0.7 for gingival and dermal cells, respectively) at day 1 of culture; they possessed a more elongated appearance (with form factors equal to 0.3 and 0.15 for gingival and dermal cells, respectively) at day 7. Continuous (gingival) and discontinuous (dermal) layers of cells were evidenced at the cortex of lattices. Contractions were associated with a significant reduction of the diameters of collagen fibers. Re-organization of substratum, as analyzed by the "Rose of Directions" technique, was evidenced only at the vicinity of filipodia where fibers ran parallel to these protrusions. Several lvsed matrix cavities were observed when fibrin lattices were populated with gingival but not dermal fibroblasts at day 5 of culture. Although cells in fibrin lattices exhibited morphometric parameters comparable with those in collagen lattices, no fibroblast layers could be demonstrated at gel peripheries. Fibrin matrices consisted of an isotropic network of entangled fibrin filaments from the start of culture, and only a slight reduction of the diameters of fibrin fibers could be evidenced in dermal fibroblast-populated lattices. Fibrinolysis at the vicinity of gingival fibroblasts led to an entire re-organization of substratum toward the formation of larger fibers. The differential behavior of gingival vs. dermal fibroblasts inside fibrin but not collagen matrices could therefore partly explain the increased rate of remodeling of gingiva as compared with dermis.
Key Words: fibroblasts collagen lattices fibrin lattices gingiva skin
Journal of Dental Research, Vol. 77, No. 9,
1717-1729 (1998) This article has been cited by other articles:
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