Zimmer B, Hartung H P, Scharfenberger G, Bitter-Suermann D, Hadding U
Eur J Immunol. 1982 May;12(5):426-30. doi: 10.1002/eji.1830120513.
To quantitate the secretion of complement component C3 by guinea pig peritoneal macrophages an enzyme-linked immunosorbent assay was developed. C3 secretion was studied in resident, elicited and activated macrophages and compared with release of hemolytically active C2 and C4, as well as the lysosomal enzyme beta-D-2-acetamido-2-deoxyglucosidase. Resident macrophages secreted about 6 ng C3/10(6) cells/h into culture supernatants over a period of 12 h. Corynebacterium parvum-activated cells were found to secrete 3 times that amount at nearly constant rates. There was a stepwise increase in secretion of functional C2 and C4 when comparing resident, elicited and activated macrophages; secretion was 2--4 times higher in activated than in resident cells.
为了定量豚鼠腹腔巨噬细胞补体成分C3的分泌,开发了一种酶联免疫吸附测定法。研究了驻留、诱导和活化巨噬细胞中的C3分泌,并将其与具有溶血活性的C2和C4以及溶酶体酶β-D-2-乙酰氨基-2-脱氧葡萄糖苷酶的释放进行比较。驻留巨噬细胞在12小时内以约6 ng C3/10(6) 个细胞/小时的速度分泌到培养上清液中。发现短小棒状杆菌活化的细胞以几乎恒定的速率分泌该量的3倍。比较驻留、诱导和活化巨噬细胞时,功能性C2和C4的分泌呈逐步增加;活化细胞中的分泌比驻留细胞高2至4倍。