Figure 5.
Effects of ELT on cell proliferation and apoptosis. The effects of ELT on cell proliferation and apoptosis were assessed on day 7 of culture using EdU incorporation and TUNEL assays, respectively. (A) Representative FACS density plots showing EdU incorporation in different cell populations. (B) Representative FACS density plots showing the TUNEL+ fraction in different cell populations. (C) In EdU incorporation assays, 30 µM of ELT significantly suppressed the proliferation of CD34+CD41+ and CD34−CD41+ cells cultured in iron-depleted conditions, a finding that was reversed by increased iron availability in culture. In contrast, CD34+/CD41− cells cultured with TPO only had significantly higher EdU incorporation when cultured in iron-depleted conditions. (D) Thirty µM of ELT also induced apoptosis in all 3 cell populations, but increased iron availability did not significantly reduce the level of apoptosis. Data reflect the mean ± SD of 5 independent experiments. *P < .05; ***P < .001.

Effects of ELT on cell proliferation and apoptosis. The effects of ELT on cell proliferation and apoptosis were assessed on day 7 of culture using EdU incorporation and TUNEL assays, respectively. (A) Representative FACS density plots showing EdU incorporation in different cell populations. (B) Representative FACS density plots showing the TUNEL+ fraction in different cell populations. (C) In EdU incorporation assays, 30 µM of ELT significantly suppressed the proliferation of CD34+CD41+ and CD34CD41+ cells cultured in iron-depleted conditions, a finding that was reversed by increased iron availability in culture. In contrast, CD34+/CD41 cells cultured with TPO only had significantly higher EdU incorporation when cultured in iron-depleted conditions. (D) Thirty µM of ELT also induced apoptosis in all 3 cell populations, but increased iron availability did not significantly reduce the level of apoptosis. Data reflect the mean ± SD of 5 independent experiments. *P < .05; ***P < .001.

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