Efficacy of copolymer scaffolds delivering human demineralised dentine matrix for bone regeneration

Poly(L-lactide-co-ε-caprolactone) scaffolds were functionalised by 10 or 20 µg/mL of human demineralised dentine matrix. Release kinetics up to 21 days and their osteogenic potential on human bone marrow stromal cells after 7 and 21 days were studied. A total of 390 proteins were identified by mass...

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Published in:Journal of tissue engineering Vol. 10; p. 2041731419852703
Main Authors: Munir, Arooj, Døskeland, Anne, Avery, Steven J, Fuoco, Tiziana, Mohamed-Ahmed, Samih, Lygre, Henning, Finne-Wistrand, Anna, Sloan, Alastair J, Waddington, Rachel J, Mustafa, Kamal, Suliman, Salwa
Format: Journal Article
Language:English
Published: London, England SAGE Publications 2019
Sage Publications Ltd
SAGE Publishing
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Summary:Poly(L-lactide-co-ε-caprolactone) scaffolds were functionalised by 10 or 20 µg/mL of human demineralised dentine matrix. Release kinetics up to 21 days and their osteogenic potential on human bone marrow stromal cells after 7 and 21 days were studied. A total of 390 proteins were identified by mass spectrometry. Bone regeneration proteins showed initial burst of release. Human bone marrow stromal cells were cultured on scaffolds physisorbed with 20 µg/mL and cultured in basal medium (DDM group) or physisorbed and cultured in osteogenic medium or cultured on non-functionalised scaffolds in osteogenic medium. The human bone marrow stromal cells proliferated less in demineralised dentine matrix group and activated ERK/1/2 after both time points. Cells on DDM group showed highest expression of IL-6 and IL-8 at 7 days and expressed higher collagen type 1 alpha 2, SPP1 and bone morphogenetic protein-2 until 21 days. Extracellular protein revealed higher collagen type 1 and bone morphogenetic protein-2 at 21 days in demineralised dentine matrix group. Cells on DDM group showed signs of mineralisation. The functionalised scaffolds were able to stimulate osteogenic differentiation of human bone marrow stromal cells.
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ISSN:2041-7314
2041-7314
DOI:10.1177/2041731419852703