4 research outputs found

    SDF-1β increases the number of surviving BMSCs following exposure to H<sub>2</sub>O<sub>2</sub>.

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    <p>Cell number of trypan blue-stained A) Tet-Off-SDF-1β BMSCs and B) Tet-Off-EV control BMSCs after vehicle control or H<sub>2</sub>O<sub>2</sub> treatment. SDF-1β significantly increased the number of surviving cells (trypan blue negative) and decreased the number of dying cells (trypan blue positive) in response to H<sub>2</sub>O<sub>2</sub> treatment compared to Dox-suppressed and Tet-Off-EV controls (6 h, ±100 ng/ml Dox, ±1.0 mM H<sub>2</sub>O<sub>2</sub>, ***p<0.0001, −Dox; H<sub>2</sub>O<sub>2</sub> vs. +Dox; H<sub>2</sub>O<sub>2</sub>, n = 3, 3 independent experiments).</p

    SDF-1β preserves BMSC nuclear morphology following exposure to H<sub>2</sub>O<sub>2</sub>.

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    <p>Representative fluorescence micrographs of Hoechst 33342-stained A) Tet-Off-SDF-1β BMSCs and B) Tet-Off-EV control BMSCs after vehicle control or H<sub>2</sub>O<sub>2</sub> treatment. Overexpression of SDF-1β in Tet-Off-SDF-1β BMSCs allows for a greater number of surviving cells and cells with preserved nuclear morphology after H<sub>2</sub>O<sub>2</sub> treatment compared to Dox-suppressed and Tet-Off-EV controls (6 h, ±100 ng/ml Dox, ±1.0 mM H<sub>2</sub>O<sub>2</sub>, 20×, 40×, bar 100 µm, n = 3, 3 independent experiments).</p

    SDF-1β does not affect BMSC proliferation.

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    <p>Colorimetric quantification of DMSO-solubilized MTT formazan at 540 nm showed no differences in proliferation of Tet-Off-SDF-1β compared to Dox-suppressed and Tet-Off-EV controls (1,3, and 7 d, ±100 ng/ml Dox, n = 6, 3 independent experiments).</p

    SDF-1β preserves BMSC morphology following exposure to H<sub>2</sub>O<sub>2</sub>.

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    <p>Representative phase contrast micrographs of A) Tet-Off-SDF-1β BMSCs and B) Tet-Off-EV control BMSCs after vehicle control or H<sub>2</sub>O<sub>2</sub> treatment. Overexpression of SDF-1β in Tet-Off-SDF-1β BMSCs allows for a greater number of cells with preserved morphology after H<sub>2</sub>O<sub>2</sub> treatment relative to Dox-suppressed and Tet-Off-EV controls (6 h, ±100 ng/ml Dox, ±1.0 mM H<sub>2</sub>O<sub>2</sub>, 20×, 40×, bar 100 µm, n = 3, 3 independent experiments).</p
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