Sci Rep. 2018 Apr 20;8(1):6307. doi: 10.1038/s41598-018-24892-0.

Combining electrical stimulation and tissue engineering to treat large bone defects in a rat model.

Leppik L¹, Zhihua H¹, Mobini S^1,2, Thottakkattumana Parameswaran V^1,3, Eischen-Loges M¹, Slavici A^1,4, Helbing J^1,5, Pindur L^1,6, Oliveira KMC¹, Bhavsar MB¹, Hudak L¹, Henrich D⁷, Barker JH⁸.

Abstract

Bone Tissue engineering (BTE) has recently been introduced as an alternative to conventional treatments for large non-healing bone defects. BTE approaches mimic autologous bone grafts, by combining cells, scaffold, and growth factors, and have the added benefit of being able to manipulate these constituents to optimize healing. Electrical stimulation (ES) has long been used to successfully treat non-healing fractures and has recently been shown to stimulate bone cells to migrate, proliferate, align, differentiate, and adhere to bio compatible scaffolds, all cell behaviors that could improve BTE treatment outcomes. With the above in mind we performed in vitro experiments and demonstrated that exposing Mesenchymal Stem Cells (MSC) + scaffold to ES for 3 weeks resulted in significant increases in osteogenic differentiation. Then in in vivo experiments, for the first time, we demonstrated that exposing BTE treated rat femur large defects to ES for 8 weeks, caused improved healing, as indicated by increased bone formation, strength, vessel density, and osteogenic gene expression. Our results demonstrate that ES significantly increases osteogenic differentiation in vitro and that this effect is translated into improved healing in vivo. These findings support the use of ES to help BTE treatments achieve their full therapeutic potential.