Hartmann J X, Galla J D, Emma D A, Kao K N, Gamborg O L
Can J Genet Cytol. 1976 Sep;18(3):503-12. doi: 10.1139/g76-062.
Polyethylene glycol (PEG) has been utilized to induce homokaryocyte formation in avian and mammalian erythrocytes previously treated with proteolytic enzymes. PEG of molecular weight 6,000-7,5000 was found superior to 1,500 and 20,000 MW PEG. Cells exposed to protease alone, prior to PEG treatment, fused to a high degree (60-95% multinucleated cells), whereas trypsin or pepsin treatment alone allowed very little fusion (2.5%). Trypsin lowered the effectiveness of protease when used in combination. Cells which were not treated with proteolytic enzymes agglutinated in the presence of PEG but did not fuse to a significant extent (0.01%). Fusion was also markedly dependent upon the rate at which PEG was eluted during the fusion process. Electron microscopy indicated that fusion began during the elution of PEG from the agglutinated cells.
聚乙二醇(PEG)已被用于在先前用蛋白水解酶处理过的禽类和哺乳动物红细胞中诱导同核体细胞形成。发现分子量为6000 - 75000的PEG优于分子量为1500和20000的PEG。在PEG处理之前仅暴露于蛋白酶的细胞高度融合(60 - 95%为多核细胞),而单独使用胰蛋白酶或胃蛋白酶处理时融合很少(2.5%)。当与蛋白酶联合使用时,胰蛋白酶会降低蛋白酶的有效性。未用蛋白水解酶处理的细胞在PEG存在下会凝集,但融合程度不显著(0.01%)。融合也明显取决于融合过程中PEG的洗脱速率。电子显微镜显示融合在PEG从凝集细胞中洗脱期间开始。