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α-干扰素和γ-干扰素可促进人急性早幼粒细胞白血病细胞系HL-60的髓系分化。

Interferon-alpha and -gamma promote myeloid differentiation of HL-60, a human acute promyelocytic leukemia cell line.

作者信息

Buessow S C, Gillespie G Y

出版信息

J Biol Response Mod. 1984 Dec;3(6):653-62.

PMID:6439829
Abstract

Two different preparations of ultrapurified interferon-alpha (IFN-alpha) (lymphoblastoid and peripheral blood leukocyte) and one of IFN-gamma were tested for their ability to induce terminal differentiation and alter cell growth in three human leukemia cell lines of different hematological origin (HL-60, K562, U937). Cell lines were cultured for 9 days in the presence of 500 units/ml of either IFN-alpha or of IFN-gamma. Cell counts and stained differentials were made on days 3, 6, and 9 to assess the effects of IFN. A marked heterogeneity of response was found, not only among cell lines, but among the IFNs tested. The most striking morphological changes were noted in the HL-60 acute promyelocytic leukemia cell line. All three IFNs tested induced significant myeloid maturation, with increased numbers of terminally differentiated myelocytes and metamyelocytes seen as early as day 3 of culture. The feasibility of using IFNs as an adjunctive or alternative therapy for the treatment of some types of leukemias is discussed.

摘要

对两种不同的超纯化α干扰素制剂(淋巴母细胞样和外周血白细胞来源)以及一种γ干扰素,检测了它们在三种不同血液学来源的人类白血病细胞系(HL-60、K562、U937)中诱导终末分化和改变细胞生长的能力。细胞系在500单位/毫升的α干扰素或γ干扰素存在下培养9天。在第3、6和9天进行细胞计数和染色分类,以评估干扰素的作用。发现不仅在细胞系之间,而且在所测试的干扰素之间,反应存在明显的异质性。在HL-60急性早幼粒细胞白血病细胞系中观察到最显著的形态学变化。所测试的所有三种干扰素均诱导了显著的髓系成熟,早在培养第3天就可见终末分化的髓细胞和晚幼粒细胞数量增加。文中讨论了将干扰素用作某些类型白血病辅助治疗或替代治疗的可行性。

相似文献

1
Interferon-alpha and -gamma promote myeloid differentiation of HL-60, a human acute promyelocytic leukemia cell line.α-干扰素和γ-干扰素可促进人急性早幼粒细胞白血病细胞系HL-60的髓系分化。
J Biol Response Mod. 1984 Dec;3(6):653-62.
2
Distinct differentiation-inducing activities of gamma-interferon and cytokine factors acting on the human promyelocytic leukemia cell line HL-60.γ-干扰素及作用于人类早幼粒细胞白血病细胞系HL-60的细胞因子的独特分化诱导活性。
Cancer Res. 1985 Jul;45(7):3090-5.
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IFI 16 gene encodes a nuclear protein whose expression is induced by interferons in human myeloid leukaemia cell lines.IFI 16基因编码一种核蛋白,其表达在人髓系白血病细胞系中由干扰素诱导。
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Gamma interferon and 1,25 dihydroxyvitamin D3 cooperate in the induction of monocytoid differentiation but not in the functional activation of the HL-60 promyelocytic leukemia cell line.γ干扰素和1,25-二羟维生素D3协同诱导单核细胞样分化,但对HL-60早幼粒细胞白血病细胞系的功能激活没有协同作用。
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Recombinant gamma-interferon and lipopolysaccharide enhance 1,25-dihydroxyvitamin D3-induced cell differentiation in human promyelocytic leukemia (HL-60) cells.重组γ-干扰素和脂多糖增强1,25-二羟维生素D3诱导的人早幼粒细胞白血病(HL-60)细胞的分化。
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Cooperative effects of gamma interferon and 1-alpha,25-dihydroxyvitamin D3 in inducing differentiation of human promyelocytic leukemia (HL-60) cells.γ干扰素与1-α,25-二羟基维生素D3在诱导人早幼粒细胞白血病(HL-60)细胞分化中的协同作用。
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Cooperative regulation of c-myc expression in differentiation of human promyelocytic leukemia induced by recombinant gamma-interferon and 1,25-dihydroxyvitamin D3.重组γ-干扰素和1,25-二羟基维生素D3诱导人早幼粒细胞白血病分化过程中c-myc表达的协同调节
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Induction of human HL-60 leukemic cell differentiation by immune interferon is accompanied by an increase in NADase activity and by a decrease in DNA-binding proteins.免疫干扰素诱导人HL-60白血病细胞分化的过程中,伴随着NAD酶活性的增加和DNA结合蛋白的减少。
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Interferon-inducible gene expression in HL-60 cells: effects of the state of differentiation.HL-60细胞中干扰素诱导的基因表达:分化状态的影响
Cell Growth Differ. 1992 Jun;3(6):369-75.

引用本文的文献

1
Interferon gamma and granulocyte/macrophage colony-stimulating factor inhibit growth and induce antigens characteristic of myeloid differentiation in small-cell lung cancer cell lines.γ干扰素和粒细胞/巨噬细胞集落刺激因子可抑制小细胞肺癌细胞系的生长并诱导髓系分化特征性抗原的产生。
Proc Natl Acad Sci U S A. 1986 Sep;83(17):6613-7. doi: 10.1073/pnas.83.17.6613.
2
Demonstration and partial characterization of the interferon-gamma receptor on human mononuclear phagocytes.人单核吞噬细胞上干扰素-γ受体的证实及部分特性分析
J Clin Invest. 1985 Dec;76(6):2196-205. doi: 10.1172/JCI112228.
3
The effect of interferons on cellular differentiation.
干扰素对细胞分化的作用。
Blut. 1986 Nov;53(5):361-70. doi: 10.1007/BF00321098.