超氧阴离子抑制猪气道平滑肌细胞的细胞内钙反应

Ramesh Krishnan, Mathur S. Kannan, Deepak Deshpande
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摘要

背景:超氧阴离子(O2-)对肺实质有多种影响,可改变细胞增殖、细胞代谢和气道平滑肌(ASM)收缩。细胞内 Ca2+ 浓度([Ca2+]i)在调节 ASM 收缩、松弛、增殖和基因表达方面起着重要作用。目的:我们研究了 O2- 对激动剂刺激 ASM 细胞中[Ca2+]i 变化的影响。设计/方法:使用装载了 Fura-2 AM 的新鲜分离的猪 ASM(PASM)细胞,在细胞外钙存在或不存在的情况下,检测其对乙酰胆碱(ACh)、组胺、内皮素、咖啡因和硫辛酸的[Ca2+]i 释放反应。结果:将 PASM 细胞暴露于黄嘌呤和黄嘌呤氧化酶(X+XO)会产生与时间相关的 O2-,并被超氧化物歧化酶(SOD)抑制。与对照细胞相比,用 X+XO 预孵育 PASM 细胞 15 或 45 分钟可抑制细胞对 ACh、组胺、咖啡因和 Thapsigargin 的净[Ca2+]i 反应。用 SOD 预处理 PASM 细胞 30 分钟可减轻 X+XO 处理对 ACh 诱导的 Ca2+ 升高的抑制作用,这表明 O2-起了作用。X+XO 处理还抑制了咖啡因和硫辛加精诱导的 Ca2+ 升高,这表明 O2- 对细胞内钙释放和再摄取机制有影响:结论:超氧化物会减弱[Ca2+]i的释放和再摄取,并可能干扰ASM细胞的生理功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Superoxide anions inhibit intracellular calcium response in porcine airway smooth muscle cells.
BACKGROUND: Superoxide anions (O2-) have multiple effects on pulmonary parenchyma altering cell proliferation, cellular metabolism, and airway smooth muscle (ASM) contraction. Intracellular Ca2+ concentration ([Ca2+]i) plays a significant role in the regulation of ASM contraction, relaxation, proliferation, and gene expression. OBJECTIVE: We investigated the effects of O2- on agonist-stimulated changes in [Ca2+]i in ASM cells. DESIGN/METHODS: Fura-2 AM-loaded, freshly isolated porcine ASM (PASM) cells were used to examine [Ca2+]i release in response to acetylcholine (ACh), histamine, endothelin, caffeine, and thapsigargin in the presence or absence of extracellular calcium. RESULTS: Exposure of PASM cells to xanthine and xanthine oxidase (X+XO) resulted in a time-dependent generation of O2-, inhibited by superoxide dismutase (SOD). Pre-incubating PASM cells with X+XO for 15- or 45-min inhibited net [Ca2+]i responses to ACh, Histamine, Caffeine, and Thapsigargin compared to control cells. Pretreating PASM cells with SOD for 30 min mitigated the inhibitory effect of X+XO treatment on ACh-induced Ca2+ elevation suggesting role of O2-. X+XO treatment also inhibited caffeine-and thapsigargin-induced Ca2+ elevation suggesting effect of O2- on intracellular calcium release and reuptake mechanisms. CONCLUSIONS: Superoxide attenuates [Ca2+]i release, reuptake and may interfere with physiological functions of ASM cells.
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