Pretreatment of Mesenchymal Stem Cells with Electrical Stimulation as a Strategy to Improve Bone Tissue Engineering Outcomes

被引:8
作者
Bianconi, Santiago [1 ]
Oliveira, Karla M. C. [1 ]
Klein, Kari-Leticia [1 ]
Wolf, Jakob [1 ]
Schaible, Alexander [1 ]
Schroeder, Katrin [2 ]
Barker, John [3 ]
Marzi, Ingo [1 ]
Leppik, Liudmila [1 ]
Henrich, Dirk [1 ]
机构
[1] Goethe Univ Frankfurt, Univ Hosp, Dept Trauma Hand & Reconstruct Surg, D-60590 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Vasc Res Ctr, D-60590 Frankfurt, Germany
[3] Goethe Univ Frankfurt, Frankfurt Initiat Regenerat Med, Expt Orthoped & Trauma Surg, D-60528 Frankfurt, Germany
关键词
electrical stimulation; bone healing; bone tissue engineering; critical size bone defect; bone marrow derived mesenchymal stem cells; beta-tricalcium phosphate; ENDOTHELIAL PROGENITOR CELLS; OSTEOGENIC DIFFERENTIATION; EARLY VASCULARIZATION; STROMAL CELLS; MARROW; POLARIZATION; REGENERATION; ENHANCE; DEFECT; ROLES;
D O I
10.3390/cells12172151
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Electrical stimulation (EStim), whether used alone or in combination with bone tissue engineering (BTE) approaches, has been shown to promote bone healing. In our previous in vitro studies, mesenchymal stem cells (MSCs) were exposed to EStim and a sustained, long-lasting increase in osteogenic activity was observed. Based on these findings, we hypothesized that pretreating MSC with EStim, in 2D or 3D cultures, before using them to treat large bone defects would improve BTE treatments. Critical size femur defects were created in 120 Sprague-Dawley rats and treated with scaffold granules seeded with MSCs that were pre-exposed or not (control group) to EStim 1 h/day for 7 days in 2D (MSCs alone) or 3D culture (MSCs + scaffolds). Bone healing was assessed at 1, 4, and 8 weeks post-surgery. In all groups, the percentage of new bone increased, while fibrous tissue and CD68+ cell count decreased over time. However, these and other healing features, like mineral density, bending stiffness, the amount of new bone and cartilage, and the gene expression of osteogenic markers, did not significantly differ between groups. Based on these findings, it appears that the bone healing environment could counteract the long-term, pro-osteogenic effects of EStim seen in our in vitro studies. Thus, EStim seems to be more effective when administered directly and continuously at the defect site during bone healing, as indicated by our previous studies.
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页数:20
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