Hypoxia Alters Progression of the Erythroid Program

Hypoxia can induce erythropoiesis through regulated increase of erythropoietin (Epo) production. We investigated the direct influence of oxygen tension (pO 2 ) in the physiologic range (2–8%) on erythroid progenitor cell differentiation using cultures of adult human hematopoietic progenitor cells exposed to decreasing (20% to 2%) pO 2 and independent of variation in Epo levels. Decreases in hemoglobin (Hb)-containing cells were observed at the end of the culture period with decreasing pO 2 . This is due, in part, to a reduction in cell growth and, at 2% O 2 , a marked increase in cell toxicity. Analysis of the kinetics of cell differentiation showed an increase in the proportion of cells with glycophorin-A expression and Hb accumulation at physiologic pO 2 . Cells were characterized by an early induction of γ-globin expression and a delay and reduction in peak levels of β-globin expression. Overall, fetal Hb and γ-globin expression were increased at physiologic pO 2 , but these increases were reduced at 2% O 2 as cultures become cytotoxic. At reduced pO 2 , induction of Epo-receptor (Epo-R) by Epo was decreased and delayed, analogous to the delay in β-globin induction. The oxygen-dependent reduction of Epo-R can account for the associated cytotoxicity at 2% O 2 . Epo induction of erythroid transcription factors, EKLF, GATA-1, and SCL/Tal-1, was also delayed and decreased at reduced pO 2 , consistent with lower levels of Epo-R and resultant Epo signaling. These changes in Epo-R and globin gene expression raise the possibility that the early increase of γ-globin is a consequence of reduced Epo signaling and a delay in induction of erythroid transcription factors.