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Role of mitochondria in modulation of spontaneous Ca2+ waves in freshly dispersed interstitial cells of Cajal from the rabbit urethra

机译:线粒体在家兔尿道新鲜分布的Cajal间质细胞中自发Ca2 +波调节中的作用

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摘要

Interstitial cells of Cajal (ICC) isolated from the rabbit urethra exhibit pacemaker activity that results from spontaneous Ca2+ waves. The purpose of this study was to investigate if this activity was influenced by Ca2+ uptake into mitochondria. Spontaneous Ca2+ waves were recorded using a Nipkow spinning disk confocal microscope and spontaneous transient inward currents (STICs) were recorded using the whole-cell patch clamp technique. Disruption of the mitochondrial membrane potential with the electron transport chain inhibitors rotenone (10 μm) and antimycin A (5 μm) abolished Ca2+ waves and increased basal Ca2+ levels. Similar results were achieved when mitochondria membrane potential was collapsed using the protonophores FCCP (0.2 μm) and CCCP (1 μm). Spontaneous Ca2+ waves were not inhibited by the ATP synthase inhibitor oligomycin (1 μm), suggesting that these effects were not attributable to an effect on ATP levels. STICs recorded under voltage clamp at −60 mV were also inhibited by CCCP and antimycin A. Dialysis of cells with the mitochondrial uniporter inhibitor RU360 (10 μm) also inhibited STICS. Stimulation of Ca2+ uptake into mitochondria using the plant flavonoid kaempferol (10 μm) induced a series of propagating Ca2+ waves. The kaempferol-induced activity was inhibited by application of caffeine (10 mm) or removal of extracellular Ca2+, but was not significantly affected by the IP3 receptor blocker 2-APB (100 μm). These data suggest that spontaneous Ca2+ waves in urethral ICC are regulated by buffering of cytoplasmic Ca2+ by mitochondria.
机译:从兔尿道分离出的Cajal间质细胞(ICC)表现出起搏器活性,这是由自发的Ca 2 + 波产生的。这项研究的目的是调查这种活性是否受线粒体中Ca 2 + 吸收的影响。使用Nipkow旋转盘共聚焦显微镜记录自发的Ca 2 + 波,并使用全细胞膜片钳技术记录自发的瞬时内向电流(STIC)。用电子传递链抑制剂鱼藤酮(10μm)和抗霉素A(5μm)破坏线粒体膜电位,使Ca 2 + 波消失,基础Ca 2 + 水平升高。当使用质子体FCCP(0.2μm)和CCCP(1μm)破坏线粒体膜电位时,获得了相似的结果。自发的Ca 2 + 波没有被ATP合酶抑制剂寡霉素(1μm)抑制,表明这些作用并不归因于对ATP水平的影响。 CCCP和抗霉素A也抑制了在-60 mV电压钳制下记录的STIC。用线粒体单向抑制剂RU360(10μm)透析细胞也抑制了STICS。利用植物类黄酮山emp酚(10μm)刺激Ca 2 + 吸收到线粒体中,引起一系列传播的Ca 2 + 波。施用咖啡因(10 mm)或去除细胞外Ca 2 + 都抑制了山萘酚诱导的活性,但不受IP3受体阻滞剂2-APB(100μm)的影响。这些数据表明,尿液ICC中的自发Ca 2 + 波受线粒体对细胞质Ca 2 + 的缓冲作用。

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