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雌激素对大鼠腹膜肥大细胞和人嗜碱性粒细胞组胺释放的调节作用。

Modulation of rat peritoneal mast cell and human basophil histamine release by estrogens.

作者信息

Cocchiara R, Albeggiani G, Di Trapani G, Azzolina A, Lampiasi N, Rizzo F, Geraci D

机构信息

Istituto di Biologia dello Sviluppo, CNR, Palermo, Italia.

出版信息

Int Arch Allergy Appl Immunol. 1990;93(2-3):192-7. doi: 10.1159/000235300.

Abstract

This study was undertaken to investigate the effect of estrogens on the histamine release mediated by IgE in rat peritoneal mast cells (PMC) and in sensitized human basophils. The estrogens were found to enhance the histamine release of either rat PMC and sensitized human basophils upon stimulation with anti-IgE. The enhancement was estrogens dose-dependent reaching the maximum value of 23% for rat PMC and 41% for sensitized human basophils stimulated with anti-IgE upon preincubation with 10(-8) M estrogens. Moreover, when purified PMC were used, the enhancing effect was still detected, suggesting a direct interaction between estrogens and mast cells. The enhancing effect took place quite rapidly reaching plateau levels in about 60 min. Basophils preincubated at 4 instead of 37 degrees C did not give any appreciable enhancement, suggesting that it was temperature-dependent and that the effect observed was not due to cytotoxicity. Incubation of PMC or human basophils with estrogens alone, without challenge with anti-IgE, did not give any detectable histamine release. The enhancement of histamine release by estrogens is probably mediated by IgE molecules present on the cell membrane, since this effect was not observed on challenge with substance P or compound 48/80, two segretagogues known to induce histamine release not via IgE.

摘要

本研究旨在探讨雌激素对大鼠腹腔肥大细胞(PMC)和致敏人嗜碱性粒细胞中由IgE介导的组胺释放的影响。发现雌激素可增强抗IgE刺激后大鼠PMC和致敏人嗜碱性粒细胞的组胺释放。这种增强呈雌激素剂量依赖性,在用10(-8)M雌激素预孵育后,抗IgE刺激的大鼠PMC组胺释放最大值达23%,致敏人嗜碱性粒细胞达41%。此外,使用纯化的PMC时,仍可检测到增强作用,提示雌激素与肥大细胞之间存在直接相互作用。增强作用发生迅速,约60分钟达到平台期。在4℃而非37℃预孵育的嗜碱性粒细胞未出现明显增强,提示其具有温度依赖性,且观察到的效应并非由细胞毒性引起。单独用雌激素孵育PMC或人嗜碱性粒细胞而不给予抗IgE刺激,未检测到组胺释放。雌激素对组胺释放的增强作用可能是由细胞膜上存在 的IgE分子介导的,因为在用P物质或48/80化合物刺激时未观察到这种效应,这两种促分泌剂已知不是通过IgE诱导组胺释放的。

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