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过氧化氢对大鼠肥大细胞功能的影响。

Hydrogen peroxide effects on rat mast cell function.

作者信息

Peden D B, Dailey L, DeGraff W, Mitchell J B, Lee J G, Kaliner M A, Hohman R J

机构信息

Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill 27599.

出版信息

Am J Physiol. 1994 Jul;267(1 Pt 1):L85-93. doi: 10.1152/ajplung.1994.267.1.L85.

DOI:10.1152/ajplung.1994.267.1.L85
PMID:8048546
Abstract

Oxidant exposure of the airway mucosa may play a significant role in the pathophysiology of asthma and allergic rhinitis. Mast cells play an important role in asthma, and oxidant exposure has been reported to cause direct mast cell degranulation as well as augment immunoglobulin E (IgE)-mediated responses in vivo. H2O2 is an oxidant generated by inflammatory cells and by the interaction of ozone with lipids or aqueous solutions. In this study, the RBL-2H3 mast cell line was used to investigate the ability of H2O2 to induce mast cell responses as well as to effect mast cell responses to IgE and the calcium ionophore A23187. Although cytotoxicity of RBL-2H3 cells at the membrane level was not observed with any concentration of H2O2, DNA damage resulted from exposure to 0.2 and 2.0 mM H2O2, and cell proliferation was inhibited by 0.075-0.2 mM H2O2. RBL cell prostaglandin D2 generation was enhanced after 60- and 120-min exposure to 0.2-20 mM H2O2. Direct serotonin release required 120-min exposures to 2.0 mM and 60-min exposures to 20 mM H2O2. However, degranulation responses induced by either IgE or A23178 were diminished after exposure to 0.2-2.0 mM H2O2. Lesser amounts (0.005-0.02 mM) had no effect on mast cell function. In summary, H2O2-induced responses of RBL cells, as well as modification of responses to IgE and A23187, occurred only at high concentrations of H2O2, which also induced both intracellular damage and inhibition of cell proliferation. Concentrations of H2O2 more likely to be physiologically relevant had no effect on mast cell responses or cytotoxicity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

气道黏膜的氧化剂暴露可能在哮喘和变应性鼻炎的病理生理学中起重要作用。肥大细胞在哮喘中起重要作用,据报道氧化剂暴露可导致肥大细胞直接脱颗粒,并增强体内免疫球蛋白E(IgE)介导的反应。过氧化氢(H2O2)是由炎症细胞以及臭氧与脂质或水溶液相互作用产生的一种氧化剂。在本研究中,使用RBL-2H3肥大细胞系来研究H2O2诱导肥大细胞反应的能力,以及影响肥大细胞对IgE和钙离子载体A23187的反应。尽管任何浓度的H2O2均未观察到RBL-2H3细胞在膜水平的细胞毒性,但暴露于0.2 mM和2.0 mM H2O2会导致DNA损伤,0.075 - 0.2 mM H2O2会抑制细胞增殖。暴露于0.2 - 20 mM H2O2 60分钟和120分钟后,RBL细胞前列腺素D2的生成增加。直接释放5-羟色胺需要暴露于2.0 mM H2O2 120分钟和暴露于20 mM H2O2 60分钟。然而,暴露于0.2 - 2.0 mM H2O2后,由IgE或A23178诱导的脱颗粒反应减弱。较少量(0.005 - 0.02 mM)对肥大细胞功能无影响。总之,H2O2诱导的RBL细胞反应以及对IgE和A23187反应的改变仅在高浓度H2O2时发生,高浓度H2O2还会诱导细胞内损伤和细胞增殖抑制。更可能具有生理相关性的H2O2浓度对肥大细胞反应或细胞毒性无影响。(摘要截短至250字)

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