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首页> 外文期刊>The biochemical journal >Biosynthesis of the third component of complement (C3) by the human monocytic-cell line U-937 Induction by phorbol myristate acetate
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Biosynthesis of the third component of complement (C3) by the human monocytic-cell line U-937 Induction by phorbol myristate acetate

机译:佛波醇肉豆蔻酸酯乙酸盐通过人单核细胞系U-937诱导补体(C3)第三成分的生物合成

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pPhorbol myristate acetate (PMA)-stimulated human monocyte-like cells (U-937) were found to synthesize the third component of complement (C3), as shown by enzyme-linked immunosorbent assay and immunoprecipitation from [35S]methionine-labelled culture supernatants. C3 synthesis occurred at a rate of about 160 ng of C3/24 h per 10(6) cells on day 7 after addition of PMA; it was blocked by cycloheximide treatment and was restored after removal of the inhibitor. SDS/polyacrylamide-gel-electrophoretic analysis of the immunoprecipitated protein showed that the size and subunit structure of the newly synthesized C3 were identical with those of plasma C3, and that a single-chain intracellular precursor was present in the cell lysates. Haemolytic assays showed that the synthesized C3 fully expressed functional activity in early culture within 4 h. After longer culture, a loss of haemolytic activity was observed. The possibility that newly secreted C3 is cleaved by U-937 cells themselves was suggested./p
机译:如酶联免疫吸附试验和[35S]蛋氨酸的免疫沉淀法所示,发现由甲酚肉豆蔻酸酯乙酸(PMA)刺激的人单核细胞样细胞(U-937)合成了补体(C3)的第三种成分。标记的培养上清液。加入PMA后第7天,C10的合成速率为每10(6)个细胞约160 ng C3 / 24 h。它被环己酰亚胺处理所阻断,并在去除抑制剂后得以恢复。免疫沉淀蛋白的SDS /聚丙烯酰胺凝胶电泳分析表明,新合成的C3的大小和亚基结构与血浆C3相同,并且细胞裂解物中存在单链细胞内前体。溶血分析表明,合成的C3在4 h的早期培养中完全表达了功能活性。长时间培养后,观察到溶血活性降低。有人提出新分泌的C3可能被U-937细胞裂解。

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