Suresh A, Sodhi A
Department of Zoology, Banaras Hindu University, Varanasi, India.
Immunol Lett. 1991 Sep;30(1):93-100. doi: 10.1016/0165-2478(91)90095-r.
Mature macrophages derived in vitro from bone marrow progenitors under the influence of either L929 CM (a source of M-CSF) or GM-CSF have been shown to differ morphologically and functionally. Treatment of these bone marrow-derived macrophages with cisplatin or LPS resulted in the expression of enhanced tumoricidal activity and the production of significant amounts of extracellular and membrane-associated IL-1 and TNF. rGM-CSF-derived bone marrow macrophages produced higher amounts of TNF and IL-1 activity than L929CM-derived macrophages. Untreated bone marrow-derived macrophages showed little IL-1 and TNF activity. Bone marrow macrophages cultured with medium alone also did not respond to cisplatin or LPS for the production of IL-1 and TNF. Neutralization studies with anti-IL-1 and anti-TNF antibodies inhibited the IL-1 and TNF activity of bone marrow-derived macrophages. These results suggest that cisplatin or LPS treatment of murine bone marrow-derived macrophages results in increased expression of both released and membrane-associated IL-1 and TNF.
在L929细胞条件培养基(一种M-CSF来源)或GM-CSF的影响下,由骨髓祖细胞体外诱导产生的成熟巨噬细胞在形态和功能上已显示出差异。用顺铂或脂多糖处理这些骨髓来源的巨噬细胞,会导致其杀肿瘤活性增强,并产生大量细胞外和膜相关的白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)。与L929细胞条件培养基诱导产生的骨髓巨噬细胞相比,GM-CSF诱导产生的骨髓巨噬细胞产生的TNF和IL-1活性更高。未经处理的骨髓来源巨噬细胞几乎没有IL-1和TNF活性。单独用培养基培养的骨髓巨噬细胞对顺铂或脂多糖刺激也不产生IL-1和TNF。用抗IL-1和抗TNF抗体进行的中和研究抑制了骨髓来源巨噬细胞的IL-1和TNF活性。这些结果表明,顺铂或脂多糖处理小鼠骨髓来源巨噬细胞会导致释放型和膜相关型IL-1和TNF的表达增加。