Functionalization of 3D-Printed Titanium Scaffolds with Elastin-like Recombinamers to Improve Cell Colonization and Osteoinduction

Author:

Guillem-Marti Jordi12ORCID,Vidal Elia12,Girotti Alessandra34ORCID,Heras-Parets Aina12,Torres Diego12,Arias Francisco Javier34ORCID,Ginebra Maria-Pau125ORCID,Rodriguez-Cabello Jose Carlos6,Manero Jose Maria12

Affiliation:

1. Biomaterials, Biomechanics and Tissue Engineering (BBT), Department of Materials Science and Engineering (CEM), Universitat Politècnica de Catalunya—BarcelonaTech (UPC), 08019 Barcelona, Spain

2. Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya—BarcelonaTech (UPC), 08019 Barcelona, Spain

3. Smart Devices for NanoMedicine Group, Department of Biochemistry and Molecular Biology and Physiology, University of Valladolid, 47011 Valladolid, Spain

4. Unidad de Excelencia Instituto de Biomedicina y Genetica Molecular (IBGM), Universidad de Valladolid and Consejo Superior de Investigaciones Cientificas (CSIC), 47003 Valladolid, Spain

5. Institute for Bioengineering of Catalonia (IBEC), Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, Spain

6. BIOFORGE (Group for Advanced Materials and Nanobiotechnology), Centro de Investigación Biomédica en Red—Bioingeniería, Biomedicina y Nanomedicina (CIBER-BBN), University of Valladolid, 47011 Valladolid, Spain

Abstract

The 3D printing of titanium (Ti) offers countless possibilities for the development of personalized implants with suitable mechanical properties for different medical applications. However, the poor bioactivity of Ti is still a challenge that needs to be addressed to promote scaffold osseointegration. The aim of the present study was to functionalize Ti scaffolds with genetically modified elastin-like recombinamers (ELRs), synthetic polymeric proteins containing the elastin epitopes responsible for their mechanical properties and for promoting mesenchymal stem cell (MSC) recruitment, proliferation, and differentiation to ultimately increase scaffold osseointegration. To this end, ELRs containing specific cell-adhesive (RGD) and/or osteoinductive (SNA15) moieties were covalently attached to Ti scaffolds. Cell adhesion, proliferation, and colonization were enhanced on those scaffolds functionalized with RGD-ELR, while differentiation was promoted on those with SNA15-ELR. The combination of both RGD and SNA15 into the same ELR stimulated cell adhesion, proliferation, and differentiation, although at lower levels than those for every single moiety. These results suggest that biofunctionalization with SNA15-ELRs could modulate the cellular response to improve the osseointegration of Ti implants. Further investigation on the amount and distribution of RGD and SNA15 moieties in ELRs could improve cell adhesion, proliferation, and differentiation compared to the present study.

Funder

Ministry of Science and Innovation of Spain

EU through the European Regional Development Funds

Publisher

MDPI AG

Subject

Pharmaceutical Science

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