Gabuzda T G, Schuman M A, Silver R K, Lewis H B
J Clin Invest. 1968 Aug;47(8):1895-904. doi: 10.1172/JCI105880.
This investigation is concerned with the kinetics of the reciprocal relationship between sheep hemoglobin (Hb) A and Hb C formation in response to anemia. The relative synthesis of the hemoglobin types was assessed at various times in bone marrow erythroid cells incubated in vitro with (59)Fe. The changeover from Hb A to Hb C formation lagged by about 3 days behind the development of anemia and was complete within about 11 days. After recovery from anemia the reciprocal change back to preanemic conditions proceeded at a much slower rate, Hb C formation gradually declining to unmeasurable levels over about 25 days. Infusions of plasma with high erythropoietin titre induced the formation of relatively large quantities of Hb C in erythroid cells of nonanemic sheep, demonstrating the central importance of a humoral mechanism in the change of expression of the hemoglobin genes. THE FOLLOWING CONCLUSIONS WERE DRAWN: hemoglobin phenotype is determined at a stem cell level. Erythroid stem cells appear to undergo gradual renewal. The identity of the plasma factor which induces Hb C formation is not yet known; it is not present in plasma from nonanemic sheep, and its production is not dependent upon hemoglobin genotype. If the plasma factor turns out to be erythropoietin, then this hormone must have an important influence on the pool of erythroid stem cells.
本研究关注绵羊血红蛋白(Hb)A和Hb C在贫血反应中相互关系的动力学。在体外与(59)Fe一起孵育的骨髓红系细胞中,于不同时间评估了血红蛋白类型的相对合成情况。从Hb A形成向Hb C形成的转变比贫血发展滞后约3天,并在约11天内完成。贫血恢复后,向贫血前状态的反向转变进行得要慢得多,Hb C形成在约25天内逐渐降至无法测量的水平。输注高促红细胞生成素滴度的血浆可在非贫血绵羊的红系细胞中诱导形成相对大量的Hb C,这表明体液机制在血红蛋白基因表达变化中至关重要。得出以下结论:血红蛋白表型在干细胞水平上确定。红系干细胞似乎经历逐渐更新。诱导Hb C形成的血浆因子的身份尚不清楚;它不存在于非贫血绵羊的血浆中,其产生不依赖于血红蛋白基因型。如果血浆因子被证明是促红细胞生成素,那么这种激素必定对红系干细胞池有重要影响。