Figure 4.
Figure 4. In vitro treatment with atorvastatin and NAC demonstrated superior effects on the number, proliferation, apoptosis, and ROS levels of cultivated BM EPCs from corticosteroid-resistant ITP patients compared with corticosteroid-sensitive ITP patients. The cultivated BM EPCs from corticosteroid-resistant ITP and corticosteroid-sensitive ITP patients were incubated with atorvastatin (ST; 500 nM) or NAC (1 mM). The effects of the different treatments on representative images (left panel) and quantification (right panel) of (A) double-positive–stained (merged in yellow) with DiI–Ac-LDL (red) and FITC–UEA-I (green) (per well) (original magnification ×10), (B) tube formation inspected on an inverted light microscope (original magnification ×4), and (C) the migrated cells (blue) which were fixed and stained with crystal violet (original magnification ×10) of cultivated BM EPCs from corticosteroid-resistant ITP patients and corticosteroid-sensitive ITP patients were compared at day 7 in culture. In addition, the (D) cell number (per well), (E) ROS levels, (F) cell proliferation, and (G) apoptosis of cultivated BM EPCs from corticosteroid-resistant ITP patients and corticosteroid-sensitive ITP patients were compared at day 7 in culture. The data were expressed as fold-change relative to corticosteroid-resistant ITP. The Wilcoxon test for paired data was used to identify the drug effects. All P values <.05 were considered significant and were provided in the figure. OD, optical density.

In vitro treatment with atorvastatin and NAC demonstrated superior effects on the number, proliferation, apoptosis, and ROS levels of cultivated BM EPCs from corticosteroid-resistant ITP patients compared with corticosteroid-sensitive ITP patients. The cultivated BM EPCs from corticosteroid-resistant ITP and corticosteroid-sensitive ITP patients were incubated with atorvastatin (ST; 500 nM) or NAC (1 mM). The effects of the different treatments on representative images (left panel) and quantification (right panel) of (A) double-positive–stained (merged in yellow) with DiI–Ac-LDL (red) and FITC–UEA-I (green) (per well) (original magnification ×10), (B) tube formation inspected on an inverted light microscope (original magnification ×4), and (C) the migrated cells (blue) which were fixed and stained with crystal violet (original magnification ×10) of cultivated BM EPCs from corticosteroid-resistant ITP patients and corticosteroid-sensitive ITP patients were compared at day 7 in culture. In addition, the (D) cell number (per well), (E) ROS levels, (F) cell proliferation, and (G) apoptosis of cultivated BM EPCs from corticosteroid-resistant ITP patients and corticosteroid-sensitive ITP patients were compared at day 7 in culture. The data were expressed as fold-change relative to corticosteroid-resistant ITP. The Wilcoxon test for paired data was used to identify the drug effects. All P values <.05 were considered significant and were provided in the figure. OD, optical density.

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