地塞米松和利多卡因抑制脐带血细胞嗜酸性粒细胞生成。

Q2 Medicine
Masato Muraki, Hirohito Kita, Gerald J Gleich
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引用次数: 2

摘要

背景:嗜酸性粒细胞在变应性炎症中起重要作用。糖皮质激素已被用作抗炎药物,用于炎性疾病涉及嗜酸性粒细胞浸润。雾化利多卡因治疗某些哮喘患者有一些效果,这也是一种炎症性疾病。本研究的目的是研究地塞米松和利多卡因对白细胞介素-5培养的人脐带血单个核细胞(UCMC)模型嗜酸性粒细胞增殖和分化的影响。方法:用IL-5 (5 ng/mL)培养UCMC 4周。采用Wright-Giemsa染色和耐氰过氧化物酶染色观察地塞米松和利多卡因对嗜酸性细胞数量和形态的影响。此外,用放射免疫法测定其对培养细胞中嗜酸性粒细胞来源的神经毒素(EDN)和嗜酸性粒细胞过氧化物酶(EPX)含量的影响。结果:在IL-5的作用下,培养细胞中嗜酸性细胞数量和EDN、EPX含量呈时间依赖性增加。地塞米松治疗在1周内轻微降低嗜酸性细胞的数量,但这种作用在2-4周内消失。地塞米松处理的UCMC巨噬细胞含有更多的嗜酸性粒细胞颗粒蛋白。地塞米松可降低培养细胞中EDN和EPX的含量。利多卡因减少了培养细胞中嗜酸性细胞的数量,降低了EDN和EPX的含量。结论:地塞米松可抑制嗜酸性粒细胞颗粒蛋白的产生并诱导嗜酸性粒细胞凋亡,而利多卡因可抑制嗜酸性粒细胞的生成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dexamethasone and lidocaine suppress eosinophilopoiesis from umbilical cord blood cells.

Dexamethasone and lidocaine suppress eosinophilopoiesis from umbilical cord blood cells.

Dexamethasone and lidocaine suppress eosinophilopoiesis from umbilical cord blood cells.

Dexamethasone and lidocaine suppress eosinophilopoiesis from umbilical cord blood cells.

Background: Eosinophils play an important role in allergic inflammation. Glucocorticosteroids have been used as an anti-inflammatory medication for inflammatory diseases involving eosinophil infiltration. Some effect of nebulized lidocaine has been reported when treating certain patients with asthma, which is also an inflammatory disease. The goal of this study was to examine the effects of dexamethasone and lidocaine on eosinophil proliferation and differentiation using a model of human umbilical cord blood mononuclear cells (UCMC) cultured with IL-5.

Methods: UCMC were cultured with IL-5 (5 ng/mL) for 4 weeks. The effects of dexamethasone and lidocaine on the number and morphology of eosinophilic cells were visualized with Wright-Giemsa and cyanide-resistant peroxidase stains. Moreover, the effect on eosinophil-derived neurotoxin (EDN) and eosinophil peroxidase (EPX) contents in cultured cells were evaluated using radioimmunoassay.

Results: The number of eosinophilic cells and EDN and EPX content in cultured cells increased in a time-dependent manner in the presence of IL-5. Dexamethasone treatment slightly decreased the number of eosinophilic cells in one week, but this effect was lost in 2-4 weeks. Macrophages in cultured UCMC treated with dexamethasone contained more eosinophil granule proteins. Both EDN and EPX content in cultured cells were reduced by dexamethasone. Lidocaine decreased the number of eosinophilic cells and reduced both EDN and EPX contents in cultured cells.

Conclusions: Dexamethasone suppressed the production of eosinophil granule proteins and may also induce apoptosis of eosinophils, while lidocaine suppresses eosinophilopoiesis.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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