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肥大细胞脱颗粒及其预防的超微结构观察

Ultrastructural observations on mast cell degranulation and its prevention.

作者信息

Djaldetti M, van der Lijn E, Notti I

出版信息

Nouv Rev Fr Hematol (1978). 1979;21(2):185-96.

PMID:117429
Abstract

The surface alterations of rat peritoneal mast cells during degranulation induced by calcium chloride (CaCl2) and its prevention by salbutamol sulfate (Sal. Sulf.), chlorpheniramine maleate (CM), and disodium cromoglycate (DSCG) were followed with a scanning electron microscope. CaCl2 caused a protuberation of the cytoplasmic granules already after 30 s, an advanced degranulation after 60-75 s, and a complete destruction of the cells after 180 s of incubation. The degranulation process was prevented by Sal. Sulf., CM, and DSCG. A comparison of the surface changes induced by these agents with the ultrastructural findings observed with a transmission electron microscope showed that neither Sal. Sulf. nor CM prevented the alterations of the internal structure of the cells, suggesting that these substances act mainly on the cytoplasmic membrane. The best prevention for both the surface and the internal structure of the cells was obtained by DSCG, indicating that this substance is a stabilizer of both membrane and internal organelles of the mast cells.

摘要

用扫描电子显微镜观察了氯化钙(CaCl2)诱导大鼠腹膜肥大细胞脱颗粒过程中的表面变化,以及硫酸沙丁胺醇(Sal. Sulf.)、马来酸氯苯那敏(CM)和色甘酸钠(DSCG)对其的预防作用。CaCl2孵育30秒后即可引起细胞质颗粒的突出,60 - 75秒后脱颗粒进一步发展,180秒后细胞完全破坏。Sal. Sulf.、CM和DSCG可防止脱颗粒过程。将这些药物诱导的表面变化与透射电子显微镜观察到的超微结构结果进行比较,发现Sal. Sulf.和CM均不能防止细胞内部结构的改变,这表明这些物质主要作用于细胞质膜。DSCG对细胞表面和内部结构的预防效果最佳,表明该物质是肥大细胞膜和内部细胞器的稳定剂。

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