Papayannopoulou T, Brice M, Stamatoyannopoulos G
Proc Natl Acad Sci U S A. 1977 Jul;74(7):2923-7. doi: 10.1073/pnas.74.7.2923.
The in vitro regulation of fetal hemoglobin (HbF was investigated in clones of cultured adult human erythroid cells by in situ immunofluorescent identification of the hemoglobins synthesized. Formation of Hb F-containing clones was enhanced by erythropoietin and by culture conditions favoring the proliferation of less-differentiated stem cells of the burst-forming-unit type. Burst-forming units differed in their capacity to direct Hb F synthesis in their terminally differentiated progeny. A class of early precursors that can produce descendent stem cells with or without commitment to Hb F production was identified. The findings suggest that the capability for expression of Hb F in terminally differentiated cells of the adult is determined at the level of less-differentiated erythroid stem cells with characteristics of burst-forming units. It is proposed that the regulation of Hb F synthesis in vivo is also linked to the process of differentiation of the erythroid stem cells and that the patterns of Hb F synthesis during ontogeny reflect the attainment of progressively higher levels of differentiation of erythroid stem cells as development proceeds.
通过对合成血红蛋白进行原位免疫荧光鉴定,在培养的成人红系细胞克隆中研究了胎儿血红蛋白(HbF)的体外调节。促红细胞生成素以及有利于爆式集落形成单位类型的低分化干细胞增殖的培养条件,均可增强含HbF克隆的形成。爆式集落形成单位在其终末分化子代中指导HbF合成的能力有所不同。鉴定出了一类早期前体细胞,它们能够产生有或无产生HbF倾向的后代干细胞。这些发现表明,成人终末分化细胞中HbF表达的能力是在具有爆式集落形成单位特征的低分化红系干细胞水平上确定的。有人提出,体内HbF合成的调节也与红系干细胞的分化过程有关,并且个体发育过程中HbF合成模式反映了随着发育进行红系干细胞分化水平逐渐提高的过程。