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Mineralization behavior with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold.

Authors :
Manferdini C
Guarino V
Zini N
Raucci MG
Ferrari A
Grassi F
Gabusi E
Squarzoni S
Facchini A
Ambrosio L
Lisignoli G
Source :
Biomaterials [Biomaterials] 2010 May; Vol. 31 (14), pp. 3986-96. Date of Electronic Publication: 2010 Feb 20.
Publication Year :
2010

Abstract

A biomimetic hyaluronic acid (HA)-based polymer scaffold was analysed in vitro for its characteristics and potential to support mineralization as carrier-vehicle. Biomimetic apatite crystal nucleation on the scaffold surface was obtained by a fine control of the pH level that increased ionic solubility thus controlling apatite formation kinetic. Different concentrations of human mesenchymal stromal cells (h-MSCs) were seeded on the scaffold, osteogenesis was induced in the presence or absence of fibroblast growth factor -2 and mineralization was analysed at different time points. We found that only at the highest h-MSCs concentration tested, the cells were uniformly distributed inside and outside the scaffold and proliferation started to decrease from day 7. Electron microscopy analysis evidenced that h-MSCs produced extracellular matrix but did not establish a direct contact with the scaffold. We found mineralized calcium-positive areas mainly present along the backbone of the scaffold starting from day 21 and increasing at day 35. FGF-2 treatment did not accelerate or increase mineralization. Non-biomimetic HA-based control scaffold showed immature mineralized areas only at day 35. Our data demonstrate that the biomimetic treatment of an HA-based scaffold promotes a faster mineralization process suggesting its possible use in clinics as a support for improving bone repair.<br /> (Copyright 2010 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-5905
Volume :
31
Issue :
14
Database :
MEDLINE
Journal :
Biomaterials
Publication Type :
Academic Journal
Accession number :
20172605
Full Text :
https://doi.org/10.1016/j.biomaterials.2010.01.148