Baines P, Cormier F, Lucien N, Boffa G A
Int J Cell Cloning. 1986 Mar;4(2):103-14. doi: 10.1002/stem.5530040204.
We report the effect of four sources of hemopoietic growth factors, alone or in combination, on colony growth in serum-free cultures of bone marrow from normal mice or marrow from mice pre-treated with 5-fluorouracil (5-FU-bm). The four supplements were: mouse spleen conditioned medium (SCM, a source of multi-lineage colony-stimulating activity, multi-CSA), human placental conditioned medium (HPCM, a source of synergistic activity), pregnant mouse uterus extract (PMUE, a source of M-CSA) and erythropoietin (Epo). First, in cultures of normal marrow, only PMUE and SCM induced significant colony growth when added alone. The majority of those colonies contained granulocytes and macrophages (myeloid colonies). In Epo-supplemented cultures, only SCM supported the growth of erythroid bursts and mixed erythroid-myeloid colonies. HPCM thus appears to be a poor source of multi-CSA. Second, in cultures of 5-FU-bm, few colonies developed if any of the above supplements were added alone. Only SCM + Epo together stimulated the formation of a low number of very large, mixed erythroid/myeloid/megakaryocyte colonies. HPCM, but not SCM, synergized with PMUE to augment myeloid colony numbers. Hence, SCM appears to be a poor source of synergistic activity (SA). In cultures of 5-FU-bm already supplemented with HPCM + PMUE, the addition of Epo did not change total colony numbers but did induce erythroid differentiation in one third of the colonies present. These data suggest that multi-CSA and SA may be expressed by different factors and that 5-FU pre-treated marrow contains: a population of primitive multipotential progenitors which form large, mixed colonies in the presence of SCM + Epo, and a larger Epo-sensitive population which also requires HPCM + PMUE to form mixed colonies.
我们报告了四种造血生长因子单独或联合使用对正常小鼠骨髓或经5-氟尿嘧啶预处理的小鼠骨髓(5-FU-bm)无血清培养中集落生长的影响。这四种补充剂分别是:小鼠脾脏条件培养基(SCM,多谱系集落刺激活性来源,多-CSA)、人胎盘条件培养基(HPCM,协同活性来源)、怀孕小鼠子宫提取物(PMUE,M-CSA来源)和促红细胞生成素(Epo)。首先,在正常骨髓培养中,单独添加时只有PMUE和SCM能诱导显著的集落生长。这些集落中的大多数含有粒细胞和巨噬细胞(髓系集落)。在添加Epo的培养物中,只有SCM能支持红系爆式集落和混合红系-髓系集落的生长。因此,HPCM似乎是多-CSA的不良来源。其次,在5-FU-bm培养中,如果单独添加上述任何一种补充剂,几乎没有集落形成。只有SCM + Epo共同刺激形成少量非常大的混合红系/髓系/巨核细胞集落。HPCM与PMUE协同作用可增加髓系集落数量,但SCM则不能。因此,SCM似乎是协同活性(SA)的不良来源。在已添加HPCM + PMUE的5-FU-bm培养物中,添加Epo不会改变集落总数,但会诱导三分之一现存集落发生红系分化。这些数据表明,多-CSA和SA可能由不同因子表达,并且5-FU预处理的骨髓含有:一群原始多能祖细胞,在SCM + Epo存在下形成大的混合集落;以及一个更大的对Epo敏感的群体,其形成混合集落还需要HPCM + PMUE。