4.5 Article

Trophic Effects of Dental Pulp Stem Cells on Schwann Cells in Peripheral Nerve Regeneration

期刊

CELL TRANSPLANTATION
卷 25, 期 1, 页码 183-193

出版社

COGNIZANT COMMUNICATION CORP
DOI: 10.3727/096368915X688074

关键词

Mobilized dental pulp stem cells (MDPSCs); Peripheral nerve regeneration; Cell transplantation; Schwann cells; Trophic effect; Sciatic nerve

资金

  1. Research Grant for Longevity Sciences from the Ministry of Health, Labour and Welfare [23-10]
  2. Ministry of Education, Science, Sports and Culture, Japan [23593007]
  3. Grants-in-Aid for Scientific Research [23593007, 25861906] Funding Source: KAKEN

向作者/读者索取更多资源

Recently, mesenchymal stem cells have demonstrated a potential for neurotrophy and neurodifferentiation. We have recently isolated mobilized dental pulp stem cells (MDPSCs) using granulocyte-colony stimulating factor (G-CSF) gradient, which has high neurotrophic/angiogenic potential. The aim of this study is to investigate the effects of MDPSC transplantation on peripheral nerve regeneration. Effects of MDPSC transplantation were examined in a rat sciatic nerve defect model and compared with autografts and control conduits containing collagen scaffold. Effects of conditioned medium of MDPSCs were also evaluated in vitro. Transplantation of MDPSCs in the defect demonstrated regeneration of myelinated fibers, whose axons were significantly higher in density compared with those in autografts and control conduits only. Enhanced revascularization was also observed in the MDPSC transplants. The MDPSCs did not directly differentiate into Schwann cell phenotype; localization of these cells near Schwann cells induced several neurotrophic factors. Immunofluorescence labeling demonstrated reduced apoptosis and increased proliferation in resident Schwann cells in the MDPSC transplant compared with control conduits. These trophic effects of MDPSCs on proliferation, migration, and antiapoptosis in Schwann cells were further elucidated in vitro. The results demonstrate that MDPSCs promote axon regeneration through trophic functions, acting on Schwann cells, and promoting angiogenesis.

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