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内皮素-2(ET-2)对中性粒细胞迁移及胞质游离钙变化的影响

The effect of endothelin-2 (ET-2) on migration and changes in cytosolic free calcium of neutrophils.

作者信息

Elferink J G, de Koster B M

机构信息

Department of Medical Biochemistry, University of Leiden, Netherlands.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1996 Jan;353(2):130-5. doi: 10.1007/BF00168749.

Abstract

The effect of endothelin-2 (ET-2) on neutrophil migration and intracellular calcium was studied. Depending on the concentration, ET-2 enhanced or inhibited neutrophil migration. At low concentrations ET-2 caused a chemotactic stimulation of migration, in contrast with endothelin-1 (ET-1) which caused a chemokinetic stimulation of migration. At higher concentrations ET-2 inhibited formyl-methionyl-leucyl-phenylalanine (fMLP)-activated migration. Both activation and inhibition by ET-2 were completely dependent on extracellular Ca2+. Unlike ET-1 which caused an increase in cytosolic free Ca2+ at a concentration which stimulated migration, ET-2 caused a measurable increase of cytosolic free Ca2+ at a concentration which did not stimulate migration. This strongly suggests that there is no correlation between maximal stimulation of cytoplasmic free calcium, and maximal stimulation of migration. Influx of extracellular Ca2+ was required for both activation of migration and change in cytosolic free Ca2+, because no effect was observed in the absence of extracellular Ca2+, and because blockers of Ca(2+)-influx inhibited ET-2-activated migration. The ETA-receptor antagonist cyclo-(-D-Trp-D-Asp-Pro-D-Val-Leu) (BQ123), and the ETB-receptor antagonist [Cys11-Cys15]-endothelin-1(11-21) (IRL1038) antagonized the stimulatory effect of ET-2 on migration, and the inhibitory effect of high concentrations of ET-2 on fMLP-activated chemotaxis. This suggests that both the ETA-receptor and the ETB-receptor are involved in the stimulatory effect of low concentrations of ET-2, and in the inhibitory effect of high concentrations of ET-2.

摘要

研究了内皮素-2(ET-2)对中性粒细胞迁移和细胞内钙的影响。根据浓度不同,ET-2可增强或抑制中性粒细胞迁移。低浓度时,ET-2引起趋化性迁移刺激,这与引起迁移化学动力学刺激的内皮素-1(ET-1)相反。高浓度时,ET-2抑制甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)激活的迁移。ET-2的激活和抑制作用均完全依赖于细胞外Ca2+。与ET-1在刺激迁移的浓度下导致胞质游离Ca2+增加不同,ET-2在不刺激迁移的浓度下导致胞质游离Ca2+有可测量的增加。这强烈表明,细胞质游离钙的最大刺激与迁移的最大刺激之间没有相关性。迁移激活和胞质游离钙变化均需要细胞外Ca2+内流,因为在没有细胞外Ca2+时未观察到效应,并且Ca2+内流阻滞剂抑制ET-2激活的迁移。ETA受体拮抗剂环(-D-色氨酸-D-天冬氨酸-脯氨酸-D-缬氨酸-亮氨酸)(BQ123)和ETB受体拮抗剂[Cys11-Cys15]-内皮素-1(11-21)(IRL1038)拮抗ET-2对迁移的刺激作用以及高浓度ET-2对fMLP激活趋化性的抑制作用。这表明ETA受体和ETB受体均参与低浓度ET-2的刺激作用以及高浓度ET-2的抑制作用。

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