Calcagno M, Pérez J R, Waldo M G, Cabrera G, Weiss-Steider B
Blood. 1982 Apr;59(4):756-60.
The existence of a molecule responsible for the induction of Fc receptor (FcR) on bone marrow cells (FcR inducer, FcRI) is demonstrated in conditioned media from the macrophage-like cell line WR19M.1 activated by bacterial lipopolysaccharides. The molecular weight obtained from molecular sieving chromatography in gel and density gradient sedimentation is found to be 18,500 daltons and 16,000 daltons, respectively, with an isoelectric pH of 7.4. The factor is found to be thermolabile and trypsin sensitive. The macrophage and granulocyte inducer (MGI), also known as colony-stimulating factor (CSF) or colony-stimulating activity (CSA), is identified from the same source and found to have a molecular weight and an isoelectric pH different from FcRI. The fractions that contained the MGI did not induce FcR on bone marrow cells, while the fractions rich in FcRI did not induce colony formation.
在经细菌脂多糖激活的巨噬细胞样细胞系WR19M.1的条件培养基中,证实了存在一种可诱导骨髓细胞上Fc受体(FcR)的分子(FcR诱导剂,FcRI)。通过凝胶分子筛色谱法和密度梯度沉降法测得该分子的分子量分别为18,500道尔顿和16,000道尔顿,等电pH值为7.4。发现该因子对热不稳定且对胰蛋白酶敏感。巨噬细胞和粒细胞诱导剂(MGI),也称为集落刺激因子(CSF)或集落刺激活性(CSA),是从同一来源鉴定出来的,发现其分子量和等电pH值与FcRI不同。含有MGI的组分不会诱导骨髓细胞上的FcR,而富含FcRI的组分不会诱导集落形成。