2011 Volume No 22  pages 344-358
|  Title: Directed migration of human bone marrow mesenchymal stem cells in a physiological direct current electric field | 
| Author: Z Zhao, C Watt, A Karystinou, AJ Roelofs, CD McCaig, IR Gibson, C De Bari | 
|  Address: Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK | 
| E-mail: c.debari at abdn.ac.uk or i.r.gibson at abdn.ac.uk | 
|  Key Words: Adult human bone marrow; mesenchymal stem cells; cell migration; tissue regeneration; direct-current electric fields; osteogenesis. | 
| Publication date: November 29th 2011 | 
|  Abstract: At  sites of bone fracture, naturally-occurring electric fields (EFs) exist during  healing and may guide cell migration. In this study, we investigated whether  EFs could direct the migration of bone marrow mesenchymal stem cells (BM-MSCs),  which are known to be key players in bone formation. Human BM-MSCs were  cultured in direct current EFs of 10 to 600 mV/mm. Using time-lapse microscopy,  we demonstrated that an EF directed migration of BM-MSCs mainly to the anode. Directional migration occurred at a low threshold and with a physiological EF of ~25 mV/mm.  Increasing the EF enhanced the MSC migratory response. The migration speed  peaked at 300 mV/mm, at a rate of 42 ±1 µm/h, around double the control (no EF)  migration rate. MSCs showed sustained response to prolonged EF application in vitro up to at least 8 h. The  electrotaxis of MSCs with either early (P3-P5) or late (P7-P10) passage was  also investigated. Migration was passage-dependent with higher passage number  showing reduced directed migration, within the range of passages examined. An  EF of 200 mV/mm for 2 h did not affect cell senescence, phenotype, or  osteogenic potential of MSCs, regardless of passage number within the range  tested (P3-P10). Our findings indicate that EFs are a powerful cue in directing  migration of human MSCs in vitro. An  applied EF may be useful to control or enhance migration of MSCs during bone  healing. | 
| Article download: Pages 
                344-358 (PDF file) Supplementary file: Video 1 
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