4.7 Article

Administration of allogeneic mesenchymal stem cells in lengthening phase accelerates early bone consolidation in rat distraction osteogenesis model

Journal

STEM CELL RESEARCH & THERAPY
Volume 11, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13287-020-01635-5

Keywords

Distraction osteogenesis; Mesenchymal stem cells; Bone consolidation; Cytokines

Funding

  1. Hong Kong Government Research Grant Council, General Research Fund [14160917, 14120118, 9054014 N_CityU102/15, T13-402/17-N]
  2. National Natural Science Foundation of China [81874000, 81430049, 81772322]
  3. Hong Kong Innovation Technology Commission Funds [ITS/UIM-305]
  4. Health and Medical Research Fund [16170951]
  5. Natural Science Funding of Guangdong Province, China [2018A030313374]
  6. Peaking Plan for the construction of high-level hospital at the Affiliated Hospital of Guangdong Medical University
  7. SMART program, Lui Che Woo Institute of Innovative Medicine, The Chinese University of Hong Kong

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BackgroundDistraction osteogenesis (DO) is a surgical technique to promote bone regeneration which may require long duration for bone consolidation. Bone marrow-derived mesenchymal stem cells (MSCs) have been applied to accelerate bone formation in DO. However, the optimal time point for cell therapy in DO remains unknown. This study sought to determine the optimal time point of cell administration to achieve early bone consolidation in DO. We hypothesized that the ratio of circulating MSCs to peripheral mononuclear cells and the level of cytokines in serum might be indicators for cell administration in DO.MethodsUnilateral tibial osteotomy with an external fixator was performed in adult Sprague Dawley rats. Three days after osteotomy, the tibia was lengthened at 0.5mm/12h for 5days. At first, 5 rats were used to analyze the blood components at 6 different time points (3days before lengthening, on the day lengthening began, or 3, 6, 10, or 14days after lengthening began) by sorting circulating MSCs and measuring serum levels of stromal cell-derived factor 1 (SDF-1) and interleukin 1 beta. Then, 40 rats were used for cell therapy study. A single dose of 5x10(5) allogeneic MSCs was locally injected at the lengthening site on day 3, 6, or 10 after lengthening began, or 3 doses of MSCs were injected at the three time points. Sequential X-ray radiographs were taken weekly. Endpoint examinations included micro-computed tomography analysis, mechanical testing, histomorphometry, and histology.ResultsThe number of circulating MSCs and serum level of SDF-1 were significantly increased during lengthening, and then decreased afterwards. Single injection of MSCs during lengthening phase (on day 3, but not day 6 or 10) significantly increased bone volume fraction, mechanical maximum loading, and bone mineralization of the regenerate. Triple injections of MSCs at three time points also significantly increased bone volume and maximum loading of the regenerates.ConclusionThis study demonstrated that bone consolidation could be accelerated by a single injection of MSCs during lengthening when the ratio of peripheral MSCs to mononuclear cells and the serum SDF-1 presented at peak levels concurrently, suggesting that day 3 after lengthening began may be the optimal time point for cell therapy to promote early bone consolidation.

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