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嗜碱性粒细胞和人肺肥大细胞的渗透激活比较。

A comparison of the osmotic activation of basophils and human lung mast cells.

作者信息

Eggleston P A, Kagey-Sobotka A, Lichtenstein L M

出版信息

Am Rev Respir Dis. 1987 May;135(5):1043-8. doi: 10.1164/arrd.1987.135.5.1043.

Abstract

Basophils and mast cells release histamine in hyperosmolar environments. Osmotic release differs significantly from IgE-dependent activation and may be important in the pathophysiology of anaphylactoid reactions during intravenous infusions of hyperosmolar radiocontrast dyes and of obstructive attacks suffered by asthmatics after exercise. To confirm reported differences in osmotic activation of basophils and lung mast cells, the process was compared systematically in the 2 cell types. Both cells were activated by hyperosmolar mannitol, glucose, sucrose, and NaCl, but histamine release from basophils rose sharply to a maximum at 1,050 mOsm/kg, whereas mast cells released maximally at 700 to 750 mOsm/kg. Release was partially Ca2+-dependent in basophils but was highly Ca2+-dependent in mast cells. Release in mast cells was rapid and essentially complete by 5 min, whereas 45 to 60 min were required in basophils. The temperature optimum in both cell types was 32 degrees C, and release in both was enhanced by drugs that increase intracellular cAMP (PGE2, IBMX, and db cAMP). We conclude that osmotic activation of basophils and mast cells is a nontoxic process that differs significantly from IgE-dependent histamine release. If it does indeed participate in the pathophysiology of human disease, different treatment strategies will be required to modulate this contribution.

摘要

嗜碱性粒细胞和肥大细胞在高渗环境中释放组胺。渗透性释放与IgE依赖性激活有显著差异,在静脉输注高渗放射性造影剂期间类过敏反应的病理生理学以及哮喘患者运动后遭受的阻塞性发作中可能起重要作用。为了证实报道的嗜碱性粒细胞和肺肥大细胞渗透性激活的差异,对这两种细胞类型的这一过程进行了系统比较。两种细胞均被高渗甘露醇、葡萄糖、蔗糖和氯化钠激活,但嗜碱性粒细胞的组胺释放在1050 mOsm/kg时急剧上升至最大值,而肥大细胞在700至750 mOsm/kg时释放最大量。嗜碱性粒细胞的释放部分依赖Ca2+,而肥大细胞的释放高度依赖Ca2+。肥大细胞的释放迅速,5分钟时基本完成,而嗜碱性粒细胞则需要45至60分钟。两种细胞类型的最适温度均为32℃,增加细胞内cAMP的药物(PGE2、IBMX和二丁酰环磷腺苷)均可增强两者的释放。我们得出结论,嗜碱性粒细胞和肥大细胞的渗透性激活是一个无毒过程,与IgE依赖性组胺释放有显著差异。如果它确实参与人类疾病的病理生理学,将需要不同的治疗策略来调节这种作用。

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