LeBlanc P A, Katz H R, Russell S W
Infect Immun. 1980 Aug;29(2):520-5. doi: 10.1128/iai.29.2.520-525.1980.
Rat monoclonal antibody raised against cultured mouse bone marrow was used to detect an antigenic determinant on a discrete population of mouse mononuclear phagocytes by indirect immunofluorescence. The antigen was expressed on adherent, late-cultured bone marrow macrophages and chronic inflammatory peritoneal macrophages elicited by the injection of thioglycolate broth. Binding of the antibody to resident peritoneal or alveolar macrophages, blood monocytes, or freshly explanted bone marrow cells was not detected. Less than 10% of acute inflammatory mononuclear phagocytes expressed the antigen. The antibody did not bind detectably to lymphocytes, granulocytes, erythrocytes, fibroblasts, or the cells of several murine tumor lines. Results suggesting binding to mast cells were equivocal. The antigen was species, but not strain, specific. It was concluded that maturation, at least, was required for expression of the antigen. Results suggested that additional influences were also involved.
用针对培养的小鼠骨髓产生的大鼠单克隆抗体,通过间接免疫荧光法检测小鼠单核吞噬细胞离散群体上的一个抗原决定簇。该抗原在贴壁的、培养后期的骨髓巨噬细胞以及注射巯基乙酸盐肉汤诱导产生的慢性炎症性腹腔巨噬细胞上表达。未检测到该抗体与驻留腹腔或肺泡巨噬细胞、血液单核细胞或刚分离出的骨髓细胞结合。不到10%的急性炎症性单核吞噬细胞表达该抗原。该抗体未检测到与淋巴细胞、粒细胞、红细胞、成纤维细胞或几种小鼠肿瘤细胞系的细胞有明显结合。提示与肥大细胞结合的结果不明确。该抗原具有种属特异性,但无品系特异性。得出的结论是,至少成熟是该抗原表达所必需的。结果表明还涉及其他影响因素。