Osteostatin-coated porous titanium can improve early bone regeneration of cortical bone defects in rats

Publication date

2015-05-01

Authors

Van Der Stok, Johan
Lozano, Daniel
Chai, Yoke Chin
Yavari, Saber AminORCID 0000-0003-1677-5751ISNI 0000000419548674
Bastidas Coral, Angela P.
Verhaar, Jan A N
Gómez-Barrena, Enrique
Schrooten, Jan
Jahr, Holger
Zadpoor, Amir A.

Editors

Advisors

Supervisors

Document Type

Article

Collections

Open Access logo

License

taverne

Abstract

A promising bone graft substitute is porous titanium. Porous titanium, produced by selective laser melting (SLM), can be made as a completely open porous and load-bearing scaffold that facilitates bone regeneration through osteoconduction. In this study, the bone regenerative capacity of porous titanium is improved with a coating of osteostatin, an osteoinductive peptide that consists of the 107-111 domain of the parathyroid hormone (PTH)-related protein (PTHrP), and the effects of this osteostatin coating on bone regeneration were evaluated in vitro and in vivo. SLM-produced porous titanium received an alkali-acid-heat treatment and was coated with osteostatin through soaking in a 100? nM solution for 24? h or left uncoated. Osteostatin-coated scaffolds contained ∼0.1? μg peptide/g titanium, and in vitro 81% was released within 24? h. Human periosteum-derived osteoprogenitor cells cultured on osteostatin-coated scaffolds did not induce significant changes in osteogenic (alkaline phosphatase [ALP], collagen type 1 [Col1], osteocalcin [OCN], runt-related transcription factor 2 [Runx2]), or angiogenic (vascular endothelial growth factor [VEGF]) gene expression; however, it resulted in an upregulation of osteoprotegerin (OPG) gene expression after 24? h and a lower receptor activator of nuclear factor kappa-B ligand (RankL):OPG mRNA ratio. In vivo, osteostatin-coated, porous titanium implants increased bone regeneration in critical-sized cortical bone defects (p=0.005). Bone regeneration proceeded until 12 weeks, and femurs grafted with osteostatin-coated implants and uncoated implants recovered, respectively, 66% and 53% of the original femur torque strength (97±31 and 77±53? N·mm, not significant). In conclusion, the osteostatin coating improved bone regeneration of porous titanium. This effect was initiated after a short burst release and might be related to the observed in vitro upregulation of OPG gene expression by osteostatin in osteoprogenitor cells. Long-term beneficial effects of osteostatin-coated, porous titanium implants on bone regeneration or mechanical strength were not established here and may require optimization of the pace and dose of osteostatin release.

Keywords

Taverne, Bioengineering, Biochemistry, Biomedical Engineering, Biomaterials, General Medicine, Journal Article, Research Support, Non-U.S. Gov't

Citation

Van Der Stok, J, Lozano, D, Chai, Y C, Amin Yavari, S, Bastidas Coral, A P, Verhaar, J A N, Gómez-Barrena, E, Schrooten, J, Jahr, H, Zadpoor, A A, Esbrit, P & Weinans, H 2015, 'Osteostatin-coated porous titanium can improve early bone regeneration of cortical bone defects in rats', Tissue Engineering. Part A, vol. 21, no. 9-10, pp. 1495-1506. https://doi.org/10.1089/ten.tea.2014.0476