• Wiesław Marcol, Wojciech Ślusarczyk, Magdalena Larysz-Brysz, Tomasz Francuz, Halina Jędrzejowska-Szypułka, Krzysztof Łabuzek, and Joanna Lewin-Kowalik.
• Department of Physiology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland. Electronic address: wmarcol@tlen.pl.
• World Neurosurg. 2015 Aug 1;84(2):511-9.

Background And ObjectiveThe influence of cultured Schwann cells on injured spinal cord in rats is examined.MethodsFocal injury of spinal cord white matter at the T10 level was produced using our original non-laminectomy method with a high-pressure air stream. Schwann cells from 7-day predegenerated rat sciatic nerves were cultured, transducted with green fluorescent protein and injected into the cisterna magna (experimental group) 3 times: immediately after spinal cord injury and 3 and 7 days later. Neurons in the brainstem and motor cortex were labeled with FluoroGold (FG) delivered caudally from the injury site a week before the end of the experiment. The functional outcome and morphologic features of neuronal survival were analyzed during a 12-week follow-up. The lesions were visualized and analyzed using magnetic resonance imaging. The maximal distance of expansion of implanted cells in the spinal cord was measured and the number of FG-positive neurons in the brain was counted.ResultsRats treated with Schwann cells presented significant improvement of locomotor performance and spinal cord morphology compared with the control group. The distance covered by Schwann cells was 7 mm from the epicenter of the injury. The number of brainstem and motor cortex FG-positive neurons in the experimental group was significantly higher than in the control group.ConclusionsThe data show that activated Schwann cells are able to induce the repair of injured spinal cord white matter. The route of application of cells via the cisterna magna seemed to be useful for their delivery in spinal cord injury therapy.Copyright © 2015 Elsevier Inc. All rights reserved.

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