Vogel S N, Perera P Y, Hogan M M, Majde J A
Department of Microbiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814.
J Leukoc Biol. 1988 Aug;44(2):136-42. doi: 10.1002/jlb.44.2.136.
Macrophage differentiation is mediated by the action of a variety of environmental signals, such as cytokines and endotoxin. For in vitro analysis of macrophage differentiation, most studies utilize a basal tissue culture medium supplemented with fetal calf serum (FCS). As the composition of specific components within FCS varies enormously from lot to lot, one can never be certain that the differentiative effects observed in vitro are attributable solely to the exogenous signals provided to the cultures. In this study, primary macrophages were cultured in a basal medium supplemented either with FCS or a compositionally defined supplement, HL-1, and a spectrum of differentiative functions (i.e., induction of antiviral activity, Fc receptor-mediated phagocytosis, Ia antigen expression, and tumoricidal activity) were measured following stimulation with exogenous signals. The results indicate that the use of serum-free, defined media may provide an important approach to dissect and characterize the differentiative signals which are operative in macrophage activation.
巨噬细胞分化是由多种环境信号介导的,如细胞因子和内毒素。对于巨噬细胞分化的体外分析,大多数研究使用添加胎牛血清(FCS)的基础组织培养基。由于FCS中特定成分的组成因批次而异,人们永远无法确定体外观察到的分化效应仅归因于提供给培养物的外源性信号。在本研究中,原代巨噬细胞在添加FCS或成分明确的补充剂HL-1的基础培养基中培养,并在受到外源性信号刺激后测量一系列分化功能(即抗病毒活性的诱导、Fc受体介导的吞噬作用、Ia抗原表达和杀肿瘤活性)。结果表明,使用无血清、成分明确的培养基可能为剖析和表征巨噬细胞激活中起作用的分化信号提供一种重要方法。