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小鼠腹腔巨噬细胞对补体激活替代途径中B因子的体外合成

In vitro synthesis of factor B of the alternative pathway of complement activation by mouse peritoneal macrophages.

作者信息

Bentley C, Bitter-Suermann D, Hadding U, Brade V

出版信息

Eur J Immunol. 1976 Jun;6(6):393-8. doi: 10.1002/eji.1830060604.

Abstract

Factor B of the alternative pathway of complement activation was shown to be synthesized and secreted by unstimulated mouse peritoneal macrophages. The activity of B in the culture supernatants from macrophage monolayers was detected by consumption of C3 in reaction mixtures containing supernatant and guinea pig factors C3, D and insoluble C3b. Using a monospecific antiserum, factor B in concentrated culture supernatants was shown by immunodiffusion and immunoelectrophoresis to be identical to factor B in mouse plasma and to form a characteristic complex with cobra venom factor in the presence of D. A steady rate of factor B secretion was observed for 4 days providing the medium was changed every 24 h. Cycloheximide (0.5 mug/ml), an inhibitor of protein synthesis, caused inhibition (90%) of factor B production. Incubation of culture medium containing 14C-labeled amino acids with the macrophage monolayer resulted in incorporation of radioactivity into factor B as detected by autoradiography of precipitation lines formed with anti-B antiserum; This indicated that synthesis of factor B had occurred. In the same culture supernatants the presence of newly synthesized C3 was also demonstrated.

摘要

补体激活替代途径的B因子被证明可由未受刺激的小鼠腹腔巨噬细胞合成并分泌。通过在含有上清液以及豚鼠因子C3、D和不溶性C3b的反应混合物中C3的消耗来检测巨噬细胞单层培养上清液中B的活性。使用单特异性抗血清,通过免疫扩散和免疫电泳显示,浓缩培养上清液中的B因子与小鼠血浆中的B因子相同,并且在存在D的情况下与眼镜蛇毒因子形成特征性复合物。如果每24小时更换一次培养基,观察到B因子的分泌速率在4天内保持稳定。蛋白质合成抑制剂环己酰亚胺(0.5微克/毫升)导致B因子产生受到抑制(90%)。用含有14C标记氨基酸的培养基与巨噬细胞单层一起孵育,通过用抗B抗血清形成的沉淀线的放射自显影检测到放射性掺入到B因子中;这表明发生了B因子的合成。在相同的培养上清液中也证实了新合成的C3的存在。

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