Volume 24, Issue 9 p. 685-692

In vitro studies on periodontal ligament cells and enamel matrix derivative

Stina Gestrelius

Corresponding Author

Stina Gestrelius

BIORA AB, Malmö, Sweden

Stina Gestrelius, B10RA AB, Ideon/Malmö, S-205 12 Malmö, Sweden. Tel.: +46 40 32 13 30, Fax: +46 40 32 13 55, e-mail: [email protected]Search for more papers by this author
Christer Andersson

Christer Andersson

BIORA AB, Malmö, Sweden

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Dagny Lidström

Dagny Lidström

BIORA AB, Malmö, Sweden

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Lars Hammarström

Lars Hammarström

Center for Oral Biology, Karolinska institute, Stockholm, Sweden

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Martha Somerman

Martha Somerman

Department of Periodontics/Prevention/Geriatrics and Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA

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First published: 13 December 2005
Citations: 331

Abstract

Abstract The recognition that periodontal regeneration can be achieved has resulted in increased efforts focused on understanding the mechanisms and factors required for restoring periodontal tissues so that clinical outcomes of such therapies are more predictable than those currently being used. In vitro models provide an excellent procedure for providing clues as to the mechanisms that may be required for regeneration of tissues. The investigations here were targeted at determining the ability of enamel matrix derivative (EMD) to influence specific properties of periodontal ligament cells in vitro. Properties of cells examined included migration, attachment, proliferation, biosynthetic activity and mineral nodule formation. Immunoassays were done to determine whether or not EMD retained known polypeptide factors. Results demonstrated that EMD under in vitro conditions formed protein aggregates, thereby providing a unique environment for cell-matrix interaction. Under these conditions, EMD: (a) enhanced proliferation of PDL cells, but not of epithelial cells; (b) increased total protein production by PDL cells; (c) promoted mineral nodule formation of PDL cells, as assayed by von Kossa staining; (d) had no significant effect on migration or attachment and spreading of cells within the limits of the assay systems used here. Next, EMD was screened for possible presence of specific molecules including: GM-CSF, calbindin D, EOF, fibronectin, bFGF, γ-interferon. IL-1β, 2, 3, 6; IGF-1,2; NGF, PDGF, TNF, TGFβ. With immunoassays used, none of these molecules were identified in EMD. These in vitro studies support the concept that EMD can act as a positive matrix for cells at a regenerative site.

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