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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间质细胞中自发性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 Ca(2+) waves. The purpose of this study was to investigate if this activity was influenced by Ca(2+) uptake into mitochondria. Spontaneous Ca(2+) 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 microm) and antimycin A (5 microm) abolished Ca(2+) waves and increased basal Ca(2+) levels. Similar results were achieved when mitochondria membrane potential was collapsed using the protonophores FCCP (0.2 microm) and CCCP (1 microm). Spontaneous Ca(2+) waves were not inhibited by the ATP synthase inhibitor oligomycin (1 microm), 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 microm) also inhibited STICS. Stimulation of Ca(2+) uptake into mitochondria using the plant flavonoid kaempferol (10 microm) induced a series of propagating Ca(2+) waves. The kaempferol-induced activity was inhibited by application of caffeine (10 mm) or removal of extracellular Ca(2+), but was not significantly affected by the IP(3) receptor blocker 2-APB (100 microm). These data suggest that spontaneous Ca(2+) waves in urethral ICC are regulated by buffering of cytoplasmic Ca(2+) by mitochondria.
机译:从兔子尿道分离的Cajal(ICC)的间质细胞表现出起搏器活动,其起因于自发Ca(2+)波。这项研究的目的是调查此活动是否受线粒体中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)。与电子运输链抑制剂鱼藤酮(10微米)和抗霉素A(5微米)的线粒体膜电位破坏取消了Ca(2+)波和增加了基础Ca(2+)水平。当使用质子载体FCCP(0.2 microm)和CCCP(1 microm)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(1 microm)抑制,表明这些影响并不归因于对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(10微米)透析细胞也抑制了STICS。使用植物类黄酮山)酚(10微米)刺激线粒体吸收Ca(2+)引起一系列传播的Ca(2+)波。 Kaempferol诱导的活性被咖啡因(10 mm)的应用或细胞外Ca(2+)的去除所抑制,但不受IP(3)受体阻滞剂2-APB(100 microm)的显着影响。这些数据表明尿道ICC中的自发Ca(2+)波受线粒体的细胞质Ca(2+)缓冲作用。

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