4.5 Article

Peripheral nerve regeneration using autologous porcine skin-derived mesenchymal stem cells

Journal

Publisher

WILEY
DOI: 10.1002/term.404

Keywords

mesenchymal stem cells; skin; in vitro neuronal differentiation; in vivo peripheral nerve regeneration

Funding

  1. Korean Research Foundation
  2. Korean Government [NRF 2009-0071566]
  3. Gyeongsang National University Hospital Research Foundation [GNUHCRF-2009-005]
  4. National Research Foundation of Korea [전09A1117] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Porcine skin-derived mesenchymal stem cells (pSMSCs) were evaluated on their biological MSC characterizations and differentiation into mesenchymal lineages, along with in vitro and in vivo neural inductions. Isolated pSMSCs showed plate-adherent growth, expression of various MSC-marker proteins and transcriptional factors, and differentiation potential into mesenchymal lineages. Neuron-like cell morphology and various neural markers were highly detected at 6 h and 24 h after in vitro neural induction of pSMSCs, but their neuron-like characteristics disappeared as induction time extended to 48 and 72 h. To evaluate the in vivo peripheral nerve regeneration potential of pSMSCs, a total of 5 x 106 autologous pSMSCs labelled with tracking dye, supplemented with fibrin glue scaffold and collagen tubulization, were transplanted into the peripheral nerve defected miniature pigs. At 2 and 4 weeks after cell transplantation, well-preserved transplanted cells and remarkable in vivo nerve regeneration, including histologically complete nerve bundles, were observed in the regenerated nerve tissues. Moreover, S-100 protein and p75 nerve growth factor receptor were more highly detected in regenerated nerve fibres compared to non-cell grafted control fibres. These results suggest that autologous pSMSCs transplanted with fibrin glue scaffold can induce prominent nerve regeneration in porcine peripheral nerve defect sites. Copyright (C) 2011 John Wiley & Sons, Ltd.

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