Hamburger A W, White C P, Dunn F E
Exp Hematol. 1985 Sep;13(8):776-81.
Macrophages, isolated from malignant effusions, were cultured in vitro in media containing GCT/CM as a source of granulocyte-macrophage (GM) colony-stimulating factor (CSF). Cells were periodically examined for macrophage-specific cell surface antigens and functional activity. The number of macrophages increased sixfold during 15 days in culture. Autoradiographic studies confirmed that macrophages were incorporating 3H-Tdr. Macrophage-specific cell surface markers were retained up to five weeks in culture. Cells were also able to express macrophage-specific functions including phagocytosis and secretion of lysozyme. The results indicate that human tumor-derived macrophages may be expanded in short-term culture in the presence of GM CSF.
从恶性积液中分离出的巨噬细胞,在含有GCT/CM(作为粒细胞-巨噬细胞集落刺激因子(CSF)来源)的培养基中进行体外培养。定期检测细胞的巨噬细胞特异性细胞表面抗原和功能活性。培养15天期间,巨噬细胞数量增加了六倍。放射自显影研究证实巨噬细胞在掺入3H-Tdr。巨噬细胞特异性细胞表面标志物在培养中可保留长达五周。细胞还能够表达巨噬细胞特异性功能,包括吞噬作用和溶菌酶分泌。结果表明,在GM CSF存在下,人肿瘤来源的巨噬细胞可在短期培养中扩增。