Gonzalez Juarrero M, Mebus C A, Pan R, Revilla Y, Alonso J M, Lunney J K
Plum Island Animal Disease Center, ARS, US Department of Agriculture, Greenport, NY 11944.
Vet Immunol Immunopathol. 1992 May;32(3-4):243-59. doi: 10.1016/0165-2427(92)90049-v.
Swine leukocyte antigens (SLA) and a macrophage specific marker were monitored on porcine macrophages cultured with or without macrophage colony stimulatory factor (M-CSF) and on cells infected with African swine fever virus (ASFV). SLA expression was maximal either in the total cell extract or on the cell surface at 3-4 days of culture; after 4 days these values began to decrease. Fluorescence analyses of immunostained macrophages cultured with or without M-CSF indicated a major upward shift in the number of SLA Class I molecules on individual macrophages whereas for SLA Class II both a novel expression of Class II and an upward shift in the number of molecules per cell were evident. Infection of 3-day-old macrophage cultures with three different isolates of ASFV resulted in minor changes in surface expression of SLA Class I, SLA Class II, and macrophage markers. No differences in infection with ASFV was observed whether macrophages were SLA Class II positive or negative, nor was there blocking by anti-SLA Class I or Class II monoclonal antibodies of ASFV infection of cultured macrophages.
在用或不用巨噬细胞集落刺激因子(M-CSF)培养的猪巨噬细胞以及感染非洲猪瘟病毒(ASFV)的细胞上监测猪白细胞抗原(SLA)和一种巨噬细胞特异性标志物。SLA表达在培养3 - 4天时在总细胞提取物中或细胞表面达到最大值;4天后这些值开始下降。对用或不用M-CSF培养的免疫染色巨噬细胞进行荧光分析表明,单个巨噬细胞上SLA I类分子数量有主要的向上变化趋势,而对于SLA II类分子,II类分子有新的表达且每个细胞的分子数量有向上变化趋势。用三种不同的ASFV分离株感染3日龄巨噬细胞培养物导致SLA I类、SLA II类和巨噬细胞标志物的表面表达有微小变化。无论巨噬细胞是SLA II类阳性还是阴性,感染ASFV均未观察到差异,用抗SLA I类或II类单克隆抗体也未阻断培养巨噬细胞的ASFV感染。