4.7 Article

Human dental pulp pluripotent-like stem cells promote wound healing and muscle regeneration

期刊

STEM CELL RESEARCH & THERAPY
卷 8, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/s13287-017-0621-3

关键词

Dental pulp; Stem cells; Revascularisation; Angiogenesis; Wound healing; Muscular dystrophy; Growth factors; Cytokines

资金

  1. Opening The Future Campaign grant [[EJJ-OPTFUT-02010] CARIPLO 2015_0634]
  2. FWO grant [G088715N, G060612N, G0A8813N]
  3. GOA grant [EJJ-C2161-GOA/11/012, IUAP-VII/07 (EJJ-C4851-17/07-P)]
  4. Project Financiering Stem Cells grant [PFO3 10/019]
  5. KU Leuven Program Financing grant [PF10/014]
  6. Universitat International de Catalunya (UIC)
  7. Agencia de Gestio d'ajuts Universitaris i de Recerca, Generalitat de Catalunya [2014 SGR 1060]
  8. predoctoral grant Junior Faculty - Obra Social La Caixa
  9. UIC
  10. PhD travel grant - Boehringer Ingelheim Fonds

向作者/读者索取更多资源

Background: Dental pulp represents an easily accessible autologous source of adult stem cells. A subset of these cells, named dental pulp pluripotent-like stem cells (DPPSC), shows high plasticity and can undergo multiple population doublings, making DPPSC an appealing tool for tissue repair or maintenance. Methods: DPPSC were harvested from the dental pulp of third molars extracted from young patients. Growth factors released by DPPSC were analysed using antibody arrays. Cells were cultured in specific differentiation media and their endothelial, smooth and skeletal muscle differentiation potential was evaluated. The therapeutic potential of DPPSC was tested in a wound healing mouse model and in two genetic mouse models of muscular dystrophy (Scid/mdx and Sgcb-null Rag2-null gamma c-null). Results: DPPSC secreted several growth factors involved in angiogenesis and extracellular matrix deposition and improved vascularisation in all three murine models. Moreover, DPPSC stimulated re-epithelialisation and ameliorated collagen deposition and organisation in healing wounds. In dystrophic mice, DPPSC engrafted in the skeletal muscle of both dystrophic murine models and showed integration in muscular fibres and vessels. In addition, DPPSC treatment resulted in reduced fibrosis and collagen content, larger cross-sectional area of type II fast-glycolytic fibres and infiltration of higher numbers of proangiogenic CD206(+) macrophages. Conclusions: Overall, DPPSC represent a potential source of stem cells to enhance the wound healing process and slow down dystrophic muscle degeneration.

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