| Literature DB >> 24704694 |
Daniel Lozano1, Sandra Sánchez-Salcedo2, Sergio Portal-Núñez3, Mercedes Vila2, Ana López-Herradón3, Juan Antonio Ardura3, Francisca Mulero4, Enrique Gómez-Barrena5, María Vallet-Regí6, Pedro Esbrit3.
Abstract
Biopolymer-coated nanocrystalline hydroxyapatite (HA) made as macroporous foams which are degradable and flexible are promising candidates as orthopaedic implants. The C-terminal (107-111) epitope of parathyroid hormone-related protein (PTHrP) exhibits osteogenic properties. The main aim of this study was to evaluate whether PTHrP (107-111) loading into gelatin-glutaraldehyde biopolymer-coated HA (HAGlu) scaffolds would produce an optimal biomaterial for tissue engineering applications. HAGlu scaffolds with and without PTHrP (107-111) were implanted into a cavitary defect performed in both distal tibial metaphysis of adult rats. Animals were sacrificed after 4 weeks for histological, microcomputerized tomography and gene expression analysis of the callus. At this time, bone healing occurred only in the presence of PTHrP (107-111)-containing HAGlu implant, related to an increase in bone volume/tissue volume and trabecular thickness, cortical thickness and gene expression of osteocalcin and vascular cell adhesion molecule 1, but a decreased gene expression of Wnt inhibitors, SOST and dickkopf homolog 1. The autonomous osteogenic effect of the PTHrP (107-111)-loaded HAGlu scaffolds was confirmed in mouse and human osteoblastic cell cultures. Our findings demonstrate the advantage of loading PTHrP (107-111) into degradable HAGlu scaffolds for achieving an optimal biomaterial that is promising for low load bearing clinical applications.Entities:
Keywords: Hydroxyapatite; In vivo bone regeneration; Macroporous scaffolds; PTHrP (107-111); Rat
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Year: 2014 PMID: 24704694 DOI: 10.1016/j.actbio.2014.03.025
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947