Optimizing combination of vascular endothelial growth factor and mesenchymal stem cells on ectopic bone formation in SCID mice

C.H Dreyer, Kristian Kjærgaard, Nicholas Ditzel, Niklas Rye Jørgensen, Søren Overgaard, Ming Ding

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review

    Abstrakt

    Introduction: Insufficient blood supply may limit bone regeneration in bone defects. Vascular endothelial growth factor (VEGF) promotes angiogenesis by increasing endothelial migration. This outcome, however, could depend on time of application. Sheep mesenchymal stem cells (MSCs) in severe combined immunodeficient (SCID) mice were used in this study to evaluate optimal time points for VEGF stimulation to increase bone formation. Methods: Twenty-eight SCID (NOD.CB17-Prkdc scid/J) mice had hydroxyapatite granules seeded with 5 × 10 5 MSCs inserted subcutaneous. Pellets released VEGF on days 1–7, days 1–14, days 1–21, days 1–42, days 7–14, and days 21–42. After 8 weeks, the implant-bone-blocks were harvested, paraffin embedded, sectioned, and stained with both hematoxylin and eosin (HE) and immunohistochemistry for human vimentin (hVim) staining. Blood samples were collected for determination of bone-related biomarkers in serum. Results: The groups with 5 × 10 5 MSCs and VEGF stimulation on days 1–14 and days 1–21 showed more bone formation when compared to the control group of 5 × 10 5 MSCs alone (p < 0.01). Serum biomarkers had no significant values. The hVim staining confirmed the ovine origin of the observed ectopic bone formation. Conclusion: Optimal bone formation of MSCs was reached when stimulating with VEGF during the first 14 or 21 days after surgery.

    OriginalsprogEngelsk
    Sider (fra-til)3326-3332
    Antal sider7
    TidsskriftJournal of Biomedical Materials Research. Part A
    Vol/bind105
    Udgave nummer12
    DOI
    StatusUdgivet - dec. 2017

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    Udforsk hvilke forskningsemner 'Optimizing combination of vascular endothelial growth factor and mesenchymal stem cells on ectopic bone formation in SCID mice' indeholder.

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