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一种5-脂氧合酶的体内抑制剂MK886,在微摩尔浓度下可诱导U937细胞和慢性粒细胞白血病细胞凋亡。

An in vivo inhibitor of 5-lipoxygenase, MK886, at micromolar concentration induces apoptosis in U937 and CML cells.

作者信息

Anderson K M, Seed T, Jajeh A, Dudeja P, Byun T, Meng J, Ou D, Bonomi P, Harris J E

机构信息

Department of Medicine, Rush Medical College, Chicago, IL 60612, USA.

出版信息

Anticancer Res. 1996 Sep-Oct;16(5A):2589-99.

PMID:8917356
Abstract

MK886 (Merck Frosst) is a selective in vivo inhibitor of 5-lipoxygenase, active at nanomolar concentrations. At micromolar concentrations, it inhibited the proliferation of U937 monoblastoid cells and of cultured malignant cells from patients with chronic myelogenous leukemia. These cells became morphologically apoptotic, a form of physiologic cell death. U937 cell apoptosis was assessed by flow cytometry, ultrastructure, DNA laddering and immuno-histology for free 3'OH-DNA. MK886-induced apoptosis developed over time as cells were recruited in concert with reduction in their numbers. Some CML cells exhibited cytoplasmic changes of apoptosis without typical nuclear changes. Under conditions used for measuring Ca2+ with Fura 2, 10 micromolar MK886 increased U937 intracellular Ca2+ 4-fold or more over the 8 minute period of measurement. Since MK886 inhibits the association of arachidonic acid with the 5-lipoxygenase activating protein, altered arachidonic acid metabolism may have contributed to these results.

摘要

MK886(默克弗罗斯特公司)是一种5-脂氧合酶的选择性体内抑制剂,在纳摩尔浓度下具有活性。在微摩尔浓度时,它抑制U937单核细胞样细胞以及慢性粒细胞白血病患者培养的恶性细胞的增殖。这些细胞在形态上呈现凋亡,这是一种生理性细胞死亡形式。通过流式细胞术、超微结构、DNA梯状条带分析以及针对游离3'OH-DNA的免疫组织学方法评估U937细胞凋亡情况。随着细胞数量减少,MK886诱导的凋亡随时间发展。一些慢性粒细胞白血病细胞表现出凋亡的细胞质变化但无典型的核变化。在使用Fura 2测量Ca2+的条件下,10微摩尔的MK886在8分钟的测量期间使U937细胞内Ca2+增加4倍或更多。由于MK886抑制花生四烯酸与5-脂氧合酶激活蛋白的结合,花生四烯酸代谢改变可能导致了这些结果。

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