Combining electrical stimulation and tissue engineering to treat large bone defects in a rat model.
Liudmila LeppikZhihua HanSahba MobiniVishnu Thottakkattumana ParameswaranMaria Eischen-LogesAndrei SlaviciJudith HelbingLukas PindurKarla Mychellyne Costa OliveiraMit B BhavsarLukasz HudakDirk HenrichJohn H BarkerPublished in: Scientific reports (2018)
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.
Keyphrases
- tissue engineering
- mesenchymal stem cells
- bone mineral density
- bone marrow
- gene expression
- induced apoptosis
- soft tissue
- bone loss
- postmenopausal women
- spinal cord injury
- bone regeneration
- umbilical cord
- cell therapy
- cell cycle arrest
- dna methylation
- oxidative stress
- stem cells
- single cell
- endoplasmic reticulum stress
- cell death
- signaling pathway