Willems R, Henckaerts E, Lenjou M, Nijs G, Rodrigus I, Moulijn A C, Slegers H, Berneman Z N, Van Bockstaele D R
Laboratory of Experimental Hematology, University of Antwerp, Antwerp University Hospital, Edegem, Belgium.
Ann Hematol. 2001 Jan;80(1):17-25. doi: 10.1007/s002770000227.
In this report we show that serum has differentiation-inducing effects on primitive hematopoietic progenitor cells with the CD34++CD38- immunophenotype. Using the pre-colony forming unit (pre-CFU) assay as a model for early myelopoiesis, we compared the effects of serum-containing and serum-free media and evaluated different cytokine cocktails [interleukin (IL)-1, IL-3, IL-6, kit ligand with and without the Flt3/Flk2 ligand (FL)]. In this assay, pre-CFUs are defined as cells unable to form colonies when plated directly in semi-solid assays, but which can differentiate into CFUs when cultured in liquid medium containing early-acting cytokines. In one of the investigated serum-free media, the average myeloid expansion in liquid medium reached up to more than 50% of that obtained in serum-containing medium. In addition, our experiments revealed differences in the clonogenic output between cells cultured in serum-free medium and those cultured in serum-containing medium, demonstrating that serum has a monocyte differentiation-inducing effect on primitive hematopoietic progenitors. Also in serum-free medium, higher proportions of erythroid progenitors were generated. These differentiation-inducing effects of serum further emphasize the need for serum-free culture protocols for hematopoietic graft engineering. Addition of FL to the culture media ameliorated cellular expansion and resulted in a decrease in the proportion of erythroid and granulocyte progenitors and an increase in the proportion of monocyte progenitors. In conclusion, this study shows that good serum-free conditions are available for differentiation assays with primitive hematopoietic progenitors and demonstrates that serum and FL have biasing effects on the initial phase of hematopoietic differentiation, favoring the monocyte lineage.
在本报告中,我们表明血清对具有CD34++CD38-免疫表型的原始造血祖细胞具有分化诱导作用。我们使用前集落形成单位(pre-CFU)测定作为早期髓系造血的模型,比较了含血清和无血清培养基的作用,并评估了不同的细胞因子组合[白细胞介素(IL)-1、IL-3、IL-6、含和不含Flt3/Flk2配体(FL)的干细胞因子]。在该测定中,pre-CFUs被定义为直接接种于半固体测定中无法形成集落,但在含有早期作用细胞因子的液体培养基中培养时可分化为CFUs的细胞。在一种研究的无血清培养基中,液体培养基中的平均髓系扩增达到含血清培养基中所获扩增的50%以上。此外,我们的实验揭示了在无血清培养基中培养的细胞与在含血清培养基中培养的细胞之间克隆形成能力的差异,表明血清对原始造血祖细胞具有单核细胞分化诱导作用。同样在无血清培养基中,产生了更高比例的红系祖细胞。血清的这些分化诱导作用进一步强调了造血移植工程无血清培养方案的必要性。向培养基中添加FL改善了细胞扩增,并导致红系和粒细胞祖细胞比例降低,单核细胞祖细胞比例增加。总之,本研究表明良好的无血清条件可用于原始造血祖细胞的分化测定,并证明血清和FL对造血分化的初始阶段具有偏向作用,有利于单核细胞系。