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佛波酯诱导人髓性白血病细胞分化:表型变化及作用方式

Induction of differentiation of human myeloid leukemias by phorbol diesters: phenotypic changes and mode of action.

作者信息

Rovera G, Ferrero D, Pagliardi G L, Vartikar J, Pessano S, Bottero L, Abraham S, Lebman D

出版信息

Ann N Y Acad Sci. 1982 Dec 10;397:211-20. doi: 10.1111/j.1749-6632.1982.tb43428.x.

Abstract

Treatment with 12-O-tetradecanoyl-phorbol-13-acetate (TPA) of acute myeloblastic leukemia cells halts proliferation and induces expression of monocyte/macrophage markers. Surface characteristics of leukemic HL60 cells, as defined using a panel of monoclonal antibodies, were found to be similar to those of normal human promyelocytes. TPA treatment, however, induced a phenotype that, unlike normal monocytes, contained several myeloid-specific markers and lacked several monocyte-specific markers. TPA treatment of HL60 cells causes the rapid disappearance of the transferrin receptor from the cell surface. Because transferrin is essential for HL60 cell proliferation in culture, the disappearance of this receptor is followed by an irreversible accumulation of the cells in the G1 phase of the cell cycle. The TPA-induced arrest of cell proliferation suggests the potential of this agent in experimentally treating myeloblastic leukemias.

摘要

用12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)处理急性髓性白血病细胞可使细胞增殖停止并诱导单核细胞/巨噬细胞标志物的表达。使用一组单克隆抗体确定的白血病HL60细胞的表面特征被发现与正常人早幼粒细胞的表面特征相似。然而,TPA处理诱导出一种表型,与正常单核细胞不同,该表型含有几种髓系特异性标志物且缺乏几种单核细胞特异性标志物。用TPA处理HL60细胞会导致转铁蛋白受体从细胞表面迅速消失。由于转铁蛋白对于HL60细胞在培养中的增殖至关重要,该受体的消失随后会导致细胞在细胞周期的G1期发生不可逆的积累。TPA诱导的细胞增殖停滞表明该药物在实验性治疗髓性白血病方面具有潜力。

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