Stopka T, Zivny J H, Stopkova P, Prchal J F, Prchal J T
Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Blood. 1998 May 15;91(10):3766-72.
Erythropoietin (EPO) is a factor essential for erythroid cell proliferation, differentiation, and survival. The production of EPO by the kidneys in response to hypoxia and anemia is well documented. To determine whether EPO is also produced by hematopoietic cells, we analyzed the expression of EPO in normal human hematopoietic progenitors and in their progeny. Undifferentiated CD34(+)lin- hematopoietic progenitors do not have detectable EPO mRNA. Differentiating CD34(+) cells that are stimulated with recombinant human EPO in serum-free liquid cultures express both EPO and EPO receptor (EPOR). Because CD34(+) cells represent a heterogeneous cell population, we analyzed individual burst-forming units-erythroid (BFU-E) and nonerythroid colony-forming unit-granulocyte-macrophage colonies for EPO mRNA. Only BFU-E colonies were positive for EPO mRNA. Lysates from pooled BFU-E colonies stained positively for EPO by immunoblotting. To further confirm the intrinsic nature of erythroid EPO, we replaced extrinsic EPO in erythroid colony cultures with EPO-mimicking peptide (EMP). We show EPO expression in the EMP-stimulated BFU-Es at both mRNA and protein levels. Stimulation of bone marrow mononuclear cells (BMMCs) with EMP upregulated EPO expression. Furthermore, we found EPO and EPOR mRNAs as well as EPO protein in K562 cells, a human erythroleukemia cell line. Stimulation of K562 cells with EMP upregulated EPO expression. We suggest that EPO of erythroid origin may have a role in the regulation of erythropoiesis.
促红细胞生成素(EPO)是红系细胞增殖、分化和存活所必需的因子。肾脏在缺氧和贫血状态下产生EPO已有充分的文献记载。为了确定造血细胞是否也能产生EPO,我们分析了正常人类造血祖细胞及其子代中EPO的表达情况。未分化的CD34(+)lin-造血祖细胞检测不到EPO mRNA。在无血清液体培养中用重组人EPO刺激分化的CD34(+)细胞,可同时表达EPO和EPO受体(EPOR)。由于CD34(+)细胞代表异质性细胞群体,我们分析了单个红系爆式集落形成单位(BFU-E)和非红系集落形成单位-粒细胞-巨噬细胞集落中的EPO mRNA。只有BFU-E集落的EPO mRNA呈阳性。合并的BFU-E集落裂解物经免疫印迹检测EPO呈阳性染色。为了进一步证实红系EPO的内在性质,我们用EPO模拟肽(EMP)替代红系集落培养中的外源性EPO。我们在mRNA和蛋白水平均显示EMP刺激的BFU-E中有EPO表达。用EMP刺激骨髓单个核细胞(BMMC)可上调EPO表达。此外,我们在人红白血病细胞系K562细胞中发现了EPO和EPOR mRNA以及EPO蛋白。用EMP刺激K562细胞可上调EPO表达。我们认为红系来源的EPO可能在红细胞生成的调节中起作用。