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T van den Bos

Publications and source records attributed to T van den Bos.

21 records · Page 2Linked to original sources

Composition and metabolism of the extracellular matrix in the periodontal ligament of impeded and unimpeded rat incisors.

Potential differences were studied in the composition and metabolism of the connective tissue components (collagen, non-collagenous proteins and glycosaminoglycans) of the periodontal ligament (PDL) as a result of alterations in the rate of eruption. The amount of collagen, glycosaminoglycan (GAG) or the water content of the tissue was the same in the unimpeded and impeded situation. The only difference was in the amount of structural non-collagenous proteins: 33 per cent increase in the unimpeded PDL. The rate of turnover of insoluble collagen, structural non-collagenous proteins and the sulphated GAG, studied in vivo by administration of [3H]-proline or [35S]-sulphate, did not differ significantly in both situations: their extremely short half-lives were respectively 9.7, 3.5 and 1.7 days. Increase in the rate of eruption and hence in the remodelling process does not result in alterations in the metabolic activity of the PDL components. Their metabolism is probably already at maximal rate and may permit the more rapid rate of eruption when the opposing force of the antagonists is diminished during the non-occlusional state of the incisors.

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Perichondrium-wrapped collagenous matrices to induce chondroneogenesis: an in vitro study.

OBJECTIVE: To develop a model for cartilage regeneration in vitro, to be used for cartilage reconstruction in vivo. METHODS: Collagenous matrices were wrapped in a perichondrium layer. The matrices served as carriers to allow migration of cells from the perichondrium into the matrix. Culture conditions stimulated cell growth and proliferation. RESULTS: After 4 weeks of culturing, microscopic examination showed an increase of cell layers around the matrices but also of cells migrated into porous matrices. Immunohistochemical staining of these cultured cells expressed type II collagen intracellularly. CONCLUSIONS: This model seems appropriate to culture mucoperichondrial explants in combination with collagenous matrices. Cells migrate into the pores of the matrix, survive, and synthesize matrix components. Actual formation of cartilage has not been shown to occur. Adding growth factors to this model may influence induction of this activity.

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