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. 2018 May 29;2(11):1207–1219. doi: 10.1182/bloodadvances.2018017533

Figure 7.

Figure 7.

Stimulation of erythroid progenitor growth by calcitriol is dependent on expression of Vdr. Linneg cKit+CD71lo/neg cells were cultured for 2 days under progenitor conditions (PM) with shRNA lentiviruses targeting Vdr (shRNA1 and shRNA2) or luciferase. Mock treated and untreated cells were included as additional controls. (A) Proliferation of cKit+CD71lo/neg cells cultured in MM with or without calcitriol (n = 3). (B) Analysis of Vdr expression in Linneg cKit+CD71lo/neg cells after 2 days of culture in PM. Vdr expression levels were normalized to Ubb and are presented as percentage expression compared with the luciferase shRNA control (dotted line, 100%). (C-D) Frequency of enucleated (C) and Ter119+ (D) cells after culture for 7 days in MM. Data were analyzed using an unpaired Student t test (B-D) or using a 2-way ANOVA (A; *P < .05, A-B; **P < .01, A; ***P < .001, A). Error bars, ± SEM (n = 3).