De la Fuente M
Department of Animal Biology II (Animal Physiology), Faculty of Biological Science, Complutense University, Madrid, Spain.
APMIS. 1989 Oct;97(10):917-22. doi: 10.1111/j.1699-0463.1989.tb00498.x.
Peritoneal macrophages from AKR/J leukemic mice, a strain which spontaneously develops a virally induced T-cell lymphoma between the age of 8-12 months, were used to study any possible changes in adherence, opsonization, phagocytosis, nitroblue tetrazolium (NBT) reduction and antibody-dependent cellular cytotoxicity (ADCC). Increased adherence, opsonization and phagocytosis of particles and impaired ADCC were found when these macrophages were compared with those from tumor-free BALB/c mice. Moreover, phagocytosis and NBT reduction in macrophages from AKR/J leukemic mice were also found to be increased when compared with macrophages from AKR/J mice in their preleukemic stage. The possibility that the decline in ADCC observed, in spite of the fact that the macrophages were activated and showed an increase in other functional aspects, may be responsible for the defective surveillance of macrophages in tumor development is also discussed.
AKR/J白血病小鼠在8至12个月大时会自发发展出病毒诱导的T细胞淋巴瘤,从该品系小鼠中获取腹膜巨噬细胞,用于研究其在黏附、调理作用、吞噬作用、硝基蓝四氮唑(NBT)还原以及抗体依赖性细胞毒性(ADCC)方面可能发生的任何变化。与无肿瘤的BALB/c小鼠的巨噬细胞相比,发现这些巨噬细胞对颗粒的黏附、调理作用和吞噬作用增强,而ADCC受损。此外,与处于白血病前期的AKR/J小鼠的巨噬细胞相比,AKR/J白血病小鼠的巨噬细胞的吞噬作用和NBT还原也有所增加。尽管巨噬细胞被激活且在其他功能方面有所增强,但观察到的ADCC下降可能是肿瘤发展过程中巨噬细胞监测缺陷的原因,对此可能性也进行了讨论。