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Angiogenic activity of an enamel matrix derivative (EMD) and EMD-derived proteins: an experimental study in mice


Thoma, D S; Villar, C C; Carnes, D L; Dard, M; Chun, Y H P; Cochran, D L (2011). Angiogenic activity of an enamel matrix derivative (EMD) and EMD-derived proteins: an experimental study in mice. Journal of Clinical Periodontology, 38(3):253-260.

Abstract

OBJECTIVES:

To determine whether all or only certain proteins in an enamel matrix derivative (EMD) are angiogenic.
MATERIALS AND METHODS:

The angiogenic effect was analysed using an in vivo angiogenesis assay. Silicon tubes were filled with or without potential and known angiogenic-modulating factors: (i) an EMD parent, (ii) nine pools of EMD proteins, (iii) fibroblast growth factor/vascular endothelial growth factor and (iv) amelogenin. Silicon tubes were implanted subcutaneously in mice. Dextran-fluorescein isothiocyanate (FITC) was injected via the tail vein, mice were euthanized and tubes were retrieved. Neovascularization was determined by measuring the amount of dextran-FITC within the tubes.
RESULTS:

The greatest angiogenic potential of the EMD parent was at a weight of 125 ng, resulting in a 4.3-fold increase compared with the negative control. Five pools of EMD proteins showed a stronger angiogenic activity than the EMD parent. Pool 5 showed the greatest angiogenic activity, when compared with the negative control (8.1-fold increase) and with 125 ng of the EMD parent (4.2-fold increase). Amelogenin demonstrated a significantly higher angiogenic activity than the negative control (increase up to 4.0-fold) and the EMD parent (increase up to 1.6-fold).
CONCLUSIONS:

EMD parent, recombinant porcine amelogenin and certain pools of EMD proteins induced significant angiogenesis compared with the controls using a standardized in vivo assay.

© 2010 John Wiley & Sons A/S.

Abstract

OBJECTIVES:

To determine whether all or only certain proteins in an enamel matrix derivative (EMD) are angiogenic.
MATERIALS AND METHODS:

The angiogenic effect was analysed using an in vivo angiogenesis assay. Silicon tubes were filled with or without potential and known angiogenic-modulating factors: (i) an EMD parent, (ii) nine pools of EMD proteins, (iii) fibroblast growth factor/vascular endothelial growth factor and (iv) amelogenin. Silicon tubes were implanted subcutaneously in mice. Dextran-fluorescein isothiocyanate (FITC) was injected via the tail vein, mice were euthanized and tubes were retrieved. Neovascularization was determined by measuring the amount of dextran-FITC within the tubes.
RESULTS:

The greatest angiogenic potential of the EMD parent was at a weight of 125 ng, resulting in a 4.3-fold increase compared with the negative control. Five pools of EMD proteins showed a stronger angiogenic activity than the EMD parent. Pool 5 showed the greatest angiogenic activity, when compared with the negative control (8.1-fold increase) and with 125 ng of the EMD parent (4.2-fold increase). Amelogenin demonstrated a significantly higher angiogenic activity than the negative control (increase up to 4.0-fold) and the EMD parent (increase up to 1.6-fold).
CONCLUSIONS:

EMD parent, recombinant porcine amelogenin and certain pools of EMD proteins induced significant angiogenesis compared with the controls using a standardized in vivo assay.

© 2010 John Wiley & Sons A/S.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Center for Dental Medicine > Clinic for Fixed and Removable Prosthodontics
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:2011
Deposited On:30 Jan 2012 07:48
Last Modified:05 Apr 2016 15:29
Publisher:Wiley-Blackwell
ISSN:0303-6979
Publisher DOI:https://doi.org/10.1111/j.1600-051X.2010.01656.x
PubMed ID:21198764

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