Liggitt H D
Am J Vet Res. 1983 May;44(5):919-24.
Goat peripheral blood mononuclear cells were isolated, using Ficoll-sodium diatrozoate. Monocytes were separated by adherence and maintained in culture for up to 50 days. By 24 hours of culture and after removal of nonadherent cells, there were 94.2 +/- 5% of the adherent cells classifiable as monocytes based on nonspecific esterase staining. Greater than 98% of these cells were phagocytic. Approximately 94% had receptors for the Fc portion of bovine immunoglobulin G, and 86% had receptors for equine complement. Cytochemically, goat monocytes were positive for nonspecific esterase, acid phosphatase, glucuronidase, lactate dehydrogenase, succinic dehydrogenase, and glycogen, regardless of culture duration when tested. Results for specific esterase, peroxidase, and Sudan black staining varied from faint to negative. The esterase staining pattern of cultured monocytes was characterized by light and electron microscopies. Ultrastructurally, esterase activity was limited to the cell membrane. Intracytoplasmic esterase activity was not recognizable in normal monocytes or in monocytes containing phagocytized particles.
采用聚蔗糖-泛影酸钠法分离山羊外周血单个核细胞。通过贴壁法分离单核细胞,并在培养中维持长达50天。培养24小时并去除未贴壁细胞后,基于非特异性酯酶染色,94.2±5%的贴壁细胞可分类为单核细胞。这些细胞中超过98%具有吞噬作用。约94%的细胞具有牛免疫球蛋白G Fc段的受体,86%的细胞具有马补体的受体。细胞化学分析显示,无论培养时间长短,山羊单核细胞的非特异性酯酶、酸性磷酸酶、葡萄糖醛酸酶、乳酸脱氢酶、琥珀酸脱氢酶和糖原均呈阳性。特异性酯酶、过氧化物酶和苏丹黑染色结果从弱阳性到阴性不等。通过光镜和电镜对培养的单核细胞的酯酶染色模式进行了表征。超微结构上,酯酶活性仅限于细胞膜。在正常单核细胞或含有吞噬颗粒的单核细胞中,胞质内酯酶活性不可见。