Walker W S, Hester R B, Beelen R H
Cell Immunol. 1983 Jul 1;79(1):125-33. doi: 10.1016/0008-8749(83)90055-2.
The stability of Ia-antigen expression on murine resident peritoneal macrophages was assessed during the course of in vitro culture. Contrary to published findings with radioimmunoassays and immunofluorescence assays, the cultured cells bore Ia-antigen, as shown by their rosetting with sheep erythrocytes coupled with anti-Ia.2 monoclonal antibody. In support of this finding, cultured cells presented the copolymer of glutamine, alanine, and tyrosine (GAT) to GAT-primed T lymphocytes in an Ia-dependent manner. Thus, functional Ia antigen is present on cultured macrophages. Disappearance of the antigen after fixation of macrophages with either glutaraldehyde or paraformaldehyde, a routine procedure in the radioimmunoassays and immunofluorescence assays, explains its presumed absence on cultured cells.
在体外培养过程中评估了小鼠腹腔常驻巨噬细胞Ia抗原表达的稳定性。与放射免疫分析和免疫荧光分析已发表的结果相反,培养的细胞带有Ia抗原,这通过它们与结合了抗Ia.2单克隆抗体的绵羊红细胞形成花环得以证明。支持这一发现的是,培养的细胞以Ia依赖的方式将谷氨酰胺、丙氨酸和酪氨酸的共聚物(GAT)呈递给经GAT致敏的T淋巴细胞。因此,功能性Ia抗原存在于培养的巨噬细胞上。在用戊二醛或多聚甲醛固定巨噬细胞后抗原消失,这是放射免疫分析和免疫荧光分析中的常规步骤,解释了其在培养细胞上可能不存在的原因。