Gazzolo L, Moscovici C, Moscovici M G, Samarut J
Cell. 1979 Mar;16(3):627-38. doi: 10.1016/0092-8674(79)90036-9.
Chicken bone marrow cells were infected with three avian acute leukemia viruses (ALV)--avian myeloblastosis virus (AMV), myelocytomatosis virus strain MC29 and Mill Hill 2 virus (MH2)--and then cultured in agar in the presence of conditioned medium. Under these conditions, it was found that very few cells served as target cells for these three viruses. Density gradient separation showed that ALV target cells were found primarily in the light density fractions and might be represented by cells committed to the mononuclear phagocyte pathway. Separation of bone marrow cells on the basis of their sedimentation velocity at unit gravity suggested that MC29 and AMV did not share the same target cells. In addition, the analysis of surface receptors and functional markers characteristic of macrophages (Fc and complement receptors, phagocytosis and immune phagocytosis) indicated that the ALV-transformed cells were blocked during their differentiation. These results indicate that the transforming ability of ALV interferes with the differentiation of their target cells.
用三种禽急性白血病病毒(ALV)——禽成髓细胞瘤病毒(AMV)、髓细胞瘤病毒MC29株和米尔希尔2病毒(MH2)感染鸡骨髓细胞,然后在条件培养基存在的情况下在琼脂中培养。在这些条件下,发现极少细胞作为这三种病毒的靶细胞。密度梯度分离显示,ALV靶细胞主要存在于低密度组分中,可能由致力于单核吞噬细胞途径的细胞代表。根据骨髓细胞在单位重力下的沉降速度进行分离表明,MC29和AMV没有共同的靶细胞。此外,对巨噬细胞特征性表面受体和功能标志物(Fc和补体受体、吞噬作用和免疫吞噬作用)的分析表明,ALV转化细胞在其分化过程中受阻。这些结果表明,ALV的转化能力干扰了其靶细胞的分化。