Gahmberg C G, Nilsson K, Andersson L C
Proc Natl Acad Sci U S A. 1979 Aug;76(8):4087-91. doi: 10.1073/pnas.76.8.4087.
The human promyelocytic leukemia cell line HL-60 can be induced to undergo morphological and functional differentiation in vitro by various low molecular weight compounds. The cellular morphology changes from blastoid appearance to that of granulocytes and the cells acquire the ability to phagocytize. We here report that the surface glycoproteins specifically change during this differentiation, as shown by the neuraminidase/galactose oxidase/NaB3H4 surface-labeling technique followed by polyacrylamide slab gel electrophoresis. The most prominent change is the loss of the major glycoprotein band typical for the blast cells which has an apparent molecular weight of 160,000 and the appearance of a major surface glycoprotein band with an apparent molecular weight of 130,000. Expression of the 130,000 molecular weight band correlates with the appearance of phagocytic and chemotactic activities of the cells. It has the same molecular weight as the major surface glycoprotein of freshly isolated human blood granulocytes.
人早幼粒细胞白血病细胞系HL-60可被多种低分子量化合物诱导在体外发生形态和功能分化。细胞形态从原始样外观转变为粒细胞外观,并且细胞获得吞噬能力。我们在此报告,如通过神经氨酸酶/半乳糖氧化酶/NaB3H4表面标记技术随后进行聚丙烯酰胺平板凝胶电泳所示,在这种分化过程中表面糖蛋白会发生特异性变化。最显著的变化是原始细胞典型的主要糖蛋白条带(表观分子量为160,000)消失,以及出现一条表观分子量为130,000的主要表面糖蛋白条带。分子量为130,000的条带的表达与细胞吞噬和趋化活性的出现相关。它与新鲜分离的人血粒细胞的主要表面糖蛋白具有相同的分子量。