Back to Search Start Over

Synchronous delivery of hydroxyapatite and connective tissue growth factor derived osteoinductive peptide enhanced osteogenesis

Authors :
Anne Christine Møller
Mette Steen Toftdal
Mingdong Dong
Menglin Chen
Ruodan Xu
Annemarie Brüel
Jesper Skovhus Thomsen
Zhongyang Zhang
Frederik Dagnæs-Hansen
Source :
Xu, R, Zhang, Z, Toftdal, M S, Møller, A C, Dagnaes-Hansen, F, Dong, M, Thomsen, J S, Brüel, A & Chen, M 2019, ' Synchronous delivery of hydroxyapatite and connective tissue growth factor derived osteoinductive peptide enhanced osteogenesis ', Journal of Controlled Release, vol. 301, pp. 129-139 . https://doi.org/10.1016/j.jconrel.2019.02.037
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

In bone tissue engineering, electrospun fibrous scaffolds can provide excellent mechanical support, extracellular matrix mimicking components, such as 3D spacial fibrous environment for cell growth and controlled release of signaling molecules for osteogenesis. Here, a facile strategy comprising the incorporation of an osteogenic inductive peptide H1, derived from the cysteine knot (CT) domain of connective tissue growth factor (CTGF), in the core of Silk Fibroin (SF) was developed for osteogenic induction, synergistically with co-delivering hydroxyapatite (HA) from the shell of poly( l -lactic acid-co-e-caprolactone) (PLCL). The core-shell nanofibrous structure was confirmed by transmission electron microscopy (TEM). Furthermore, the sustained released H1 has effectively promoted proliferation and osteoblastic differentiation of human induced pluripotent stem cells-derived mesenchymal stem cells (hiPS-MSCs). Moreover, after 8 weeks implantation in mice, this SF-H1/PLCL-HA composite induced bone tissue formation significantly faster than SF/PLCL as indicated by μCT. The present study is the first to demonstrate that release of short hydrophilic peptides derived from CTGF combined with HA potentiated the regenerative capacity for healing critical sized calvarial defect in vivo.

Details

ISSN :
01683659
Volume :
301
Database :
OpenAIRE
Journal :
Journal of Controlled Release
Accession number :
edsair.doi.dedup.....c933a4838b5b72fde8edfef48d2b884b