4.5 Article

Conditioned media from mesenchymal stromal cells and periodontal ligament fibroblasts under cyclic stretch stimulation promote bone healing in mouse calvarial defects

期刊

CYTOTHERAPY
卷 22, 期 10, 页码 543-551

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jcyt.2020.05.008

关键词

bone regeneration; conditioned media; mechanotransduction; mesenchymal stem cells

资金

  1. Japan Society for the Promotion of Science KAKENHI [18K09635]
  2. Grants-in-Aid for Scientific Research [18K09635] Funding Source: KAKEN

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Background aims: When cells are exposed to stresses such as mechanical stimuli, they release growth factors and adapt to the surrounding environment Here, we demonstrated that mechanical stimulation during culture affects the production of osteogenic and angiogenic factors. Methods: Human bone marrow derived mesenchymal stromal cells (hMSCs) and human periodontal ligament fibroblasts (HPLFs ) were cultured under cyclic stretch stimulation for 24 h. Collected of the cells and conditioned media (CM), the gene and protein expression levels of osteogenic and angiogenic factors were evaluated. CM was also evaluated for angiogenic activity and calcification ability. In in vivo study, CM was administered to a mouse calvarial defect model and histologically and radiologically evaluated. Results: Quantitative real time polymerase chain reaction results showed that the expression of bone morphogenetic protein 2, 4 (BMP 2, 4), vascular endothelial growth factor A (VEGF A), and platelet derived growth factor AA (PDGF AA) was upregulated in the cyclic stretch stimulation group in comparison with the non stretch group in each cell type. Enzyme linked immunosor bent assay results revealed that the expression of BMP 2,4, VEGF A was upregulated in the cyclic stretch group in comparison with the non stretch group in each cell type. Only HPLFs showed significant difference in PDGF AA expression between the cyclic stretch and the non stretch group. Tube formation assay and Alizarin Red S staining results showed that angiogenic activity and calcification ability of CM was upregulated in the cyclic stretch stimulation group in comparison with the non stretch group in each cell type. CM was administered to the mouse calvarial defect model. Histological and radiological examination showed that the bone healing was promoted by CM from the cyclic stretch culture group. Immunohistological staining revealed that CM from cyclic stretch group have greater angiogenic effect than CM from the non stretch group. Conclusions: These results indicate that osteogenesis was promoted by CM obtained under cyclic stretch stimulation through the increase of angiogenesis in the mouse calvarial defect model. (C) 2020 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.

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