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人重组巨噬细胞集落刺激因子(M-CSF)可增加人单核细胞的Cl酯酶抑制剂(Cl-INH)合成。

Human recombinant macrophage colony-stimulating factor (M-CSF) increases Cl-esterase inhibitor (Cl-INH) synthesis by human monocytes.

作者信息

Schmidt B, Gyapay G, Válay M, Füst G

机构信息

Department of Immunopathology, National Institute of Hematology and Blood Transfusion, Budapest, Hungary.

出版信息

Immunology. 1991 Dec;74(4):677-9.

Abstract

The ability of macrophage colony-stimulating factor (M-CSF) to influence production of complement proteins by cultured human monocytes was studied. Three-day-old cultures of human monocytes were treated with 250-1000 U/ml recombinant human M-CSF (Cetus Corporation, Emeryville, CA). After 3 days the M-CSF containing medium was replaced by the same medium without M-CSF, and the cells were cultured for 3 more days. Samples taken at the removal of M-CSF and 3 days later were tested for the concentration of factor B and Cl-esterase inhibitor (Cl-INH) using ELISA methods, and C2 by using an immunohaemolytic assay. M-CSF induced a marked dose-dependent increase in the synthesis of Cl-INH, but did not significantly change Bf and C2 production. The findings suggest that M-CSF is able to influence selectively the complement protein-producing ability of cultured human monocytes.

摘要

研究了巨噬细胞集落刺激因子(M-CSF)影响培养的人单核细胞补体蛋白产生的能力。用人单核细胞进行三天的培养,并用250 - 1000 U/ml重组人M-CSF(加州埃默里维尔的塞特斯公司)处理。3天后,将含有M-CSF的培养基换成不含M-CSF的相同培养基,细胞再培养3天。在去除M-CSF时以及3天后采集的样本,使用酶联免疫吸附测定法检测B因子和C1酯酶抑制剂(C1-INH)的浓度,使用免疫溶血测定法检测C2。M-CSF诱导C1-INH的合成显著呈剂量依赖性增加,但对B因子和C2的产生没有显著影响。这些发现表明M-CSF能够选择性地影响培养的人单核细胞产生补体蛋白的能力。

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