Hovi T, Mosher D, Vaheri A
J Exp Med. 1977 Jun 1;145(6):1580-9. doi: 10.1084/jem.145.6.1580.
alpha2-Macroglobulin levels in the supernates of cultures of different subpopulations of human peripheral blood mononuclear leukocytes were assayed by a radioimmunoassay. Unfractionated mononuclear leukocytes produced greater amounts of the macroglobulin (4.0 vs. 0.8 ng/10(6) cells) than did subpopulations enriched in T or B+T lymphocytes, by passage through nylon wool or cotton wool columns, respectively. Still higher concentrations of alpha2-macroglobulin (40 ng/10(6) cells) were measured in the supernates of glass-adherent mononuclear leukocyte cultures. These results suggest that cells of monocyte-macrophage lineage are mainly, if not exclusively, responsible for the appearance of alpha2- macroglobulin in the supernate of human peripheral blood leukocyte cultures. The de novo synthesis and release of alpha2-macroglobulin by cultured monocytes was demonstrated by immunoprecipitation of radioactivity from supernates of 32S-methionine-labeled glass-adherent cells. Antiserum against purified alpha2-macroglobulin was used in both Ouchterlony double diffusion and double antibody precipitation tests. SDS-polyacrylamide gel electrophoresis of immunoprecipitates showed that most of the radioactivity comigrated with authentic alpha2-macroglobulin subunit at about 160,000 daltons.
采用放射免疫分析法测定了人外周血单个核白细胞不同亚群培养上清液中的α2-巨球蛋白水平。未分离的单个核白细胞产生的巨球蛋白量(4.0对0.8 ng/10⁶细胞)比分别通过尼龙棉或棉柱富集的T或B+T淋巴细胞亚群产生的量更多。在玻璃黏附单个核白细胞培养上清液中测得的α2-巨球蛋白浓度更高(40 ng/10⁶细胞)。这些结果表明,单核细胞-巨噬细胞谱系的细胞即使不是唯一的,也是主要负责在人外周血白细胞培养上清液中出现α2-巨球蛋白的细胞。通过对32S-甲硫氨酸标记的玻璃黏附细胞培养上清液中的放射性进行免疫沉淀,证明了培养的单核细胞可从头合成并释放α2-巨球蛋白。在双向琼脂扩散试验和双抗体沉淀试验中均使用了抗纯化α2-巨球蛋白的抗血清。免疫沉淀物的SDS-聚丙烯酰胺凝胶电泳显示,大部分放射性与约160,000道尔顿的天然α2-巨球蛋白亚基一起迁移。