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氯化锂诱导HL-60和WEHI-3B D+白血病细胞分化

Induction of the differentiation of HL-60 and WEHI-3B D+ leukemia cells by lithium chloride.

作者信息

Sokoloski J A, Li J, Nigam A, Sartorelli A C

机构信息

Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06510.

出版信息

Leuk Res. 1993 May;17(5):403-10. doi: 10.1016/0145-2126(93)90095-3.

Abstract

The use of lithium chloride in manic-depressive patients and in patients receiving myelo-suppressive cancer chemotherapeutic agents is accompanied by a sustained leukocytosis due to an increase in granulocyte production. This property suggests that lithium chloride may have effects on hematopoietic differentiation. Treatment of cultured WEHI-3B D+ murine myelomonocytic and HL-60 human promyelocytic leukemia cells with millimolar concentrations of lithium chloride resulted in concentration-dependent increases in the number of differentiated myeloid cells, as determined by the ability of the cells to reduce nitroblue tetrazolium and by the binding of myeloid specific antibodies, and was associated with an inhibition of cellular proliferation. The effects of lithium chloride on growth and differentiation were antagonized by KCl, whereas NaCl had little effect. The induction of leukemic cell maturation by lithium chloride was markedly enhanced by the addition of low levels of retinoic acid. In contrast, other differentiation inducing agents (i.e. dimethyl sulfoxide and selenazofurin) had no effect on the degree of maturation induced by lithium. These findings suggest that the combination of lithium chloride and retinoic acid may have clinical utility in the treatment of leukemia through the induction of terminal differentiation.

摘要

在躁郁症患者以及接受骨髓抑制性癌症化疗药物治疗的患者中使用氯化锂,会因粒细胞生成增加而伴随持续的白细胞增多。这一特性表明氯化锂可能对造血分化有影响。用毫摩尔浓度的氯化锂处理培养的WEHI-3B D+小鼠骨髓单核细胞和HL-60人早幼粒细胞白血病细胞,会导致分化的髓样细胞数量呈浓度依赖性增加,这是通过细胞还原硝基蓝四氮唑的能力以及髓样特异性抗体的结合来确定的,并且与细胞增殖的抑制相关。氯化钾可拮抗氯化锂对生长和分化的影响,而氯化钠几乎没有影响。添加低水平的视黄酸可显著增强氯化锂诱导白血病细胞成熟的作用。相比之下,其他分化诱导剂(即二甲基亚砜和硒唑呋林)对锂诱导的成熟程度没有影响。这些发现表明,氯化锂和视黄酸的联合使用可能通过诱导终末分化在白血病治疗中具有临床应用价值。

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