Sergeant Gerard P, Bradley Eamonn, Thornbury Keith D, McHale Noel G, Hollywood Mark A
The Smooth Muscle Research Centre, Dundalk Institute of Technology, Dundalk, Co Louth, Ireland.
J Physiol. 2008 Oct 1;586(19):4631-42. doi: 10.1113/jphysiol.2008.159194. Epub 2008 Aug 14.
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.
从兔尿道分离出的Cajal间质细胞(ICC)表现出由自发钙波引起的起搏活动。本研究的目的是调查这种活动是否受线粒体对钙的摄取影响。使用Nipkow旋转盘共聚焦显微镜记录自发钙波,使用全细胞膜片钳技术记录自发瞬时内向电流(STICs)。用电子传递链抑制剂鱼藤酮(10微摩尔)和抗霉素A(5微摩尔)破坏线粒体膜电位可消除钙波并提高基础钙水平。当使用质子载体FCCP(0.2微摩尔)和CCCP(1微摩尔)使线粒体膜电位崩溃时,也得到了类似的结果。ATP合酶抑制剂寡霉素(1微摩尔)未抑制自发钙波,表明这些作用并非归因于对ATP水平的影响。在-60 mV电压钳下记录的STICs也受到CCCP和抗霉素A的抑制。用线粒体单向转运体抑制剂RU360(10微摩尔)对细胞进行透析也抑制了STICs。使用植物黄酮山奈酚(10微摩尔)刺激线粒体对钙的摄取可诱导一系列传播的钙波。山奈酚诱导的活动可被应用咖啡因(10毫摩尔)或去除细胞外钙所抑制,但不受IP3受体阻滞剂2-APB(100微摩尔)的显著影响。这些数据表明,尿道ICC中的自发钙波受线粒体对细胞质钙的缓冲调节。