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人早幼粒细胞白血病细胞系HL60中钙及分泌反应的发展

Development of calcium and secretory responses in the human promyelocytic leukemia cell line HL60.

作者信息

Naccache P H, Molski T F, Spinelli B, Borgeat P, Abboud C N

出版信息

J Cell Physiol. 1984 May;119(2):241-6. doi: 10.1002/jcp.1041190215.

Abstract

We have begun to characterize the development of the excitation-response coupling sequence in the human promyelocytic leukemia cell line HL60. Using the recently developed fluorescent calcium probe quin-2, it was found that DMSO induced myeloid differentiation of the HL60 cells is accompanied by the development of a calcium response to the addition of the chemotactic factors fMet-Leu-Phe and leukotriene B4. The characteristics (time course, concentration dependence, stereospecificity, and metabolic dependence) of the calcium response are extremely similar to those previously described in human neutrophils. These results imply that functional receptors for leukotriene B4 appear in HL60 cells upon the induction of differentiation and also lend strong support to the use of these HL60 cells as a model of human myeloid differentiation. We have also characterized the emergence of a secretory response to fMet-Leu-Phe and leukotriene B4 in cytochalasin B treated HL60 cells. In addition, it is found that differentiation was required for the calcium ionophore A23187 to express its secretory activity toward the HL60 cells. This last set of results implies that differentiation is accompanied by the coordinated appearance of surface receptors and cytoplasmic factors required for the expression of cellular responsiveness.

摘要

我们已开始对人早幼粒细胞白血病细胞系HL60中兴奋-反应偶联序列的发育进行表征。使用最近开发的荧光钙探针喹啉-2,发现二甲基亚砜诱导的HL60细胞髓系分化伴随着对趋化因子N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(fMet-Leu-Phe)和白三烯B4添加的钙反应的发展。钙反应的特征(时间进程、浓度依赖性、立体特异性和代谢依赖性)与先前在人中性粒细胞中描述的极为相似。这些结果表明,白三烯B4的功能性受体在分化诱导后出现在HL60细胞中,也有力支持了将这些HL60细胞用作人髓系分化模型。我们还表征了在细胞松弛素B处理的HL60细胞中对fMet-Leu-Phe和白三烯B4的分泌反应的出现。此外,发现钙离子载体A23187对HL60细胞表达其分泌活性需要分化。最后这组结果表明,分化伴随着细胞反应性表达所需的表面受体和细胞质因子的协同出现。

相似文献

2
Myeloid differentiated HL-60 cells display specific leukotriene B4 binding sites.
Adv Prostaglandin Thromboxane Leukot Res. 1986;16:165-77.

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