Paul C C, Ackerman S J, Mahrer S, Tolbert M, Dvorak A M, Baumann M A
Research Service, Dayton VA Medical Center, Ohio.
J Leukoc Biol. 1994 Jul;56(1):74-9. doi: 10.1002/jlb.56.1.74.
Study of eosinophil growth and differentiation has been hampered by the difficulty of obtaining adequate numbers of highly purified eosinophil progenitors or mature eosinophils for analysis. The AML14 myeloid leukemia cell line has the unusual ability to exhibit eosinophilic differentiation in response to stimulation by combinations of the eosinophil-active cytokines interleukin-3 (IL-3), granulocyte-macrophage colony-stimulating factor, and IL-5. We now demonstrate that AML14 cells can be stimulated by a combination of these cytokines to produce mRNA encoding all the eosinophil granule proteins, including major basic protein (MBP), eosinophil peroxidase (EPO), eosinophil cationic protein (ECP), eosinophil-derived neurotoxin (EDN), and the Charcot-Leyden crystal (CLC) protein (eosinophil lysophospholipase). The production of the mature proteins was demonstrated by Western blotting, and ultrastructural analysis demonstrated the presence of immature secondary granules in cells that had been induced to differentiate to eosinophils. These findings demonstrate the utility of the AML14 cell line as a model for the study of cytokine induction of eosinophil growth and differentiation.
嗜酸性粒细胞生长和分化的研究一直受到阻碍,原因是难以获取足够数量的高度纯化的嗜酸性粒细胞祖细胞或成熟嗜酸性粒细胞用于分析。AML14髓系白血病细胞系具有不同寻常的能力,即能在嗜酸性粒细胞活性细胞因子白细胞介素-3(IL-3)、粒细胞-巨噬细胞集落刺激因子和IL-5的组合刺激下表现出嗜酸性分化。我们现在证明,这些细胞因子的组合可刺激AML14细胞产生编码所有嗜酸性粒细胞颗粒蛋白的mRNA,包括主要碱性蛋白(MBP)、嗜酸性粒细胞过氧化物酶(EPO)、嗜酸性粒细胞阳离子蛋白(ECP)、嗜酸性粒细胞衍生神经毒素(EDN)以及夏科-莱登晶体(CLC)蛋白(嗜酸性粒细胞溶血磷脂酶)。通过蛋白质印迹法证实了成熟蛋白的产生,超微结构分析表明,已诱导分化为嗜酸性粒细胞的细胞中存在未成熟的次级颗粒。这些发现证明了AML14细胞系作为研究细胞因子诱导嗜酸性粒细胞生长和分化模型的实用性。