Cabrita Inês, Benedetto Roberta, Fonseca Ana, Wanitchakool Podchanart, Sirianant Lalida, Skryabin Boris V, Schenk Laura K, Pavenstädt Hermann, Schreiber Rainer, Kunzelmann Karl
Physiological Institute, University of Regensburg, Regensburg, Germany;
Physiological Institute, University of Regensburg, Regensburg, Germany.
FASEB J. 2017 May;31(5):2123-2134. doi: 10.1096/fj.201600797RR. Epub 2017 Feb 9.
The Ca-activated Cl channel TMEM16A [anoctamin (ANO)1] is homologous to yeast Ist2 and has been shown to tether the cortical endoplasmic reticulum (ER) to the plasma membrane. We therefore examined whether ANO1 and other members of the ANO family affect intracellular Ca ([Ca]) signals. It is shown that expression of ANO1 augments Ca store release upon stimulation of GPCRs, whereas knockdown of ANO1, or lack of Ano1 expression in Ano1 animals, as shown in an earlier report, inhibits Ca release. ANO6, and -10 show similar effects, whereas expression of ANO4, -8, and -9 attenuate filling of the ER store. The impact of ANO1 and -4 were examined in more detail. ANO1 colocalized and interacted with IPR, whereas ANO4 colocalized with SERCA Ca pumps and interacted with ORAI-1 channels, respectively. ANO1 Cl currents were rapidly activated exclusively through Ca store release, and remained untouched by influx of extracellular Ca In contrast expression of ANO4 caused a delayed activation of membrane-localized ANO6 channels, solely through store-operated Ca entry ORAI. Ca signals were inhibited by knocking down expression of endogenous ANO1, -5, -6, and -10 and were also reduced in epithelial cells from Ano10 mice. The data suggest that ANOs affect compartmentalized [Ca] signals, which may explain some of the cellular defects related to ANO mutations.-Cabrita, I., Benedetto, R., Fonseca, A., Wanitchakool, P., Sirianant, L., Skryabin, B. V., Schenk, L. K., Pavenstädt, H., Schreiber, R., Kunzelmann, K. Differential effects of anoctamins on intracellular calcium signals.
钙激活氯离子通道TMEM16A [无翅型MMTV整合位点家族成员1(ANO)1] 与酵母Ist2同源,并且已被证明可将皮质内质网(ER)与质膜相连。因此,我们研究了ANO1和ANO家族的其他成员是否会影响细胞内钙离子([Ca])信号。结果表明,ANO1的表达会增强G蛋白偶联受体(GPCR)受刺激时的钙库释放,而如先前报告所示,敲低ANO1或Ano1基因敲除小鼠中缺乏Ano1表达会抑制钙释放。ANO6和-10显示出类似的作用,而ANO4、-8和-9的表达会减弱内质网钙库的充盈。我们更详细地研究了ANO1和-4的影响。ANO1与肌醇1,4,5-三磷酸受体(IPR)共定位并相互作用,而ANO4分别与肌浆网Ca2+-ATP酶(SERCA)钙泵共定位并与钙释放激活钙通道1(ORAI-)通道相互作用。ANO1氯离子电流仅通过钙库释放迅速激活,不受细胞外钙内流的影响。相比之下,ANO4的表达仅通过钙库操纵的钙内流(SOCE)ORAI导致膜定位的ANO6通道延迟激活。敲低内源性ANO1、-5、-6和-10的表达会抑制钙信号,并且Ano10小鼠的上皮细胞中的钙信号也会降低。数据表明,ANO会影响分隔的[Ca]信号,这可能解释了一些与ANO突变相关的细胞缺陷。-卡布里塔,I.,贝内代托,R.,丰塞卡,A.,瓦尼查库尔,P.,西里亚南特,L.,斯克里亚宾,B.V.,申克,L.K.,帕文施泰特,H.,施赖伯,R.,昆策尔曼,K.无翅型MMTV整合位点家族成员对细胞内钙信号的不同影响。