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Fig. 7 | Stem Cell Research & Therapy

Fig. 7

From: Human decidua basalis mesenchymal stem/stromal cells protect endothelial cell functions from oxidative stress induced by hydrogen peroxide and monocytes

Fig. 7

The proliferation of monocytes (THP-1) and HUVEC evaluated by the MTS assay. After 24 h and as compared to untreated THP-1, the proliferation of THP-1 in the presence of H2O2 and DBMSCs (THP-1/DBMSC + H2O2) significantly increased at different THP-1 and DBMSC ratios (20:1, 10:1, 5:1, and 2.5:1) (a). After 24 h and as compared with untreated HUVEC, the proliferation of H2O2-treated HUVEC (HUVEC + H2O2) and H2O2-treated HUVEC in the presence of THP-1 pretreated with H2O2 (THP-1 + H2O2) at 1:10 HUVEC:THP-1 ratio significantly increased (b). The proliferation of H2O2-treated HUVEC in the presence of THP-1 pretreated with H2O2 and DBMSCs (THP-1/DBMSC + H2O2) significantly reduced as compared with H2O2-treated HUVEC cultured with THP-1 pretreated with H2O2 (b). After 24 h culture with DBMSCs and as compared to monocytes cultured alone, the proliferation of THP-1 significantly increased at all examined ratios of monocytes and DBMSCs (a). As compared to monocytes cultured with H2O2 alone, the proliferation of monocyte cultured with DBMSCs did not significantly change, P > 0.05 (a). Each experiment was performed in triplicate and repeated for five times with five independent preparations of DBMSCs and HUVEC. *P < 0.05. Bars represent standard errors

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