Ash R C, Detrick D A, Zanjani E D
Blood. 1981 Aug;58(2):309-16.
An in vitro clonal assay for a class of human hemopoietic progenitors (CFU-GEMM) with several characteristics of pluripotential stem cells has been previously described. In the presence of medium conditioned by leukocytes stimulated with phytohemagglutinin (PHA-LCM) and erythropoietin (Ep), CFU-GEMM give rise to mixed hemopoietic colonies containing granulocytic, erythroid, monocyte-macrophage, and megakaryocytic elements. In initial studies we found that CFU-GEMM were present in equal but low frequencies in blood (B) and bone marrow (M) mononuclear cell populations. However, when the culture system was modified by the substitution of Iscove's modified Dulbecco's medium for alpha-MEM and the addition of mercaptoethanol, a significant enhancement of mixed colony formation occurred, and an approximately 3-4-fold difference in the frequency of CFU-GEMM between B and M emerged. Replating studies showed the formation of secondary differentiated hemopoietic colonies and at least a limited capacity for self-renewal of CFU-GEMM. The in vitro growth of normal CFU-GEMM was highly dependent on hemopoietin(s) present in PHA-LCM. In vitro detection of CFU-GEMM, however, requires only relatively low permissive concentrations of Ep, in contrast to the high Ep requirement for optimal BFU-E growth in vitro. These and other data described demonstrate CFU-GEMM to be a distinct multipotential stem cell class whose assay may prove useful in the study of human blood dyscrasias.
先前已描述了一种针对一类具有多能干细胞若干特性的人类造血祖细胞(CFU-GEMM)的体外克隆测定法。在由植物血凝素(PHA-LCM)刺激的白细胞和促红细胞生成素(Ep)调节的培养基存在下,CFU-GEMM产生包含粒细胞、红细胞、单核细胞-巨噬细胞和巨核细胞成分的混合造血集落。在初步研究中,我们发现CFU-GEMM在血液(B)和骨髓(M)单核细胞群体中的频率相等但较低。然而,当通过用Iscove改良的杜尔贝科培养基替代α-MEM并添加巯基乙醇来修改培养系统时,混合集落形成显著增强,并且B和M之间CFU-GEMM频率出现了约3至4倍的差异。再接种研究显示了二级分化造血集落的形成以及CFU-GEMM至少有限的自我更新能力。正常CFU-GEMM的体外生长高度依赖于PHA-LCM中存在的造血生长因子。然而,与体外最佳BFU-E生长对Ep的高需求相反,CFU-GEMM的体外检测仅需要相对较低的允许浓度的Ep。所描述的这些及其他数据表明CFU-GEMM是一种独特的多能干细胞类别,其测定法可能在人类血液发育异常的研究中证明有用。