Turvey Matthew R, Fogarty Kevin E, Thorn Peter
Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, CB2 IPD, UK.
J Cell Sci. 2005 Mar 1;118(Pt 5):971-80. doi: 10.1242/jcs.01693. Epub 2005 Feb 15.
We explored a potential structural and functional link between filamentous actin (F-actin) and inositol (1,4,5)-trisphosphate receptors (IP(3)Rs) in mouse pancreatic acinar cells. Using immunocytochemistry, F-actin and type 2 and 3 IP(3)Rs (IP(3)R2 and IP(3)R3) were identified in a cellular compartment immediately beneath the apical plasma membrane. In an effort to demonstrate that IP(3)R distribution is dependent on an intact F-actin network in the apical subplasmalemmal region, cells were treated with the actin-depolymerising agent latrunculin B. Immunocytochemistry indicated that latrunculin B treatment reduced F-actin in the basolateral subplasmalemmal compartment, and reduced and fractured F-actin in the apical subplasmalemmal compartment. This latrunculin-B-induced loss of F-actin in the apical region coincided with a reduction in IP(3)R2 and IP(3)R3, with the remaining IP(3)Rs localized with the remaining F-actin. Experiments using western blot analysis showed that IP(3)R3s are resistant to extraction by detergents, which indicates a potential interaction with the cytoskeleton. Latrunculin B treatment in whole-cell patch-clamped cells inhibited Ca(2+)-dependent Cl(-) current spikes evoked by inositol (2,4,5)-trisphosphate; this is due to an inhibition of the underlying local Ca(2+) signal. Based on these findings, we suggest that IP(3)Rs form links with F-actin in the apical domain and that these links are essential for the generation of local Ca(2+) spikes.
我们探究了小鼠胰腺腺泡细胞中丝状肌动蛋白(F-肌动蛋白)与肌醇(1,4,5)-三磷酸受体(IP₃Rs)之间潜在的结构和功能联系。运用免疫细胞化学方法,在紧邻顶端质膜下方的细胞区室中鉴定出了F-肌动蛋白以及2型和3型IP₃Rs(IP₃R2和IP₃R3)。为了证明IP₃R的分布依赖于顶端质膜下区域完整的F-肌动蛋白网络,我们用肌动蛋白解聚剂拉特肌醇B处理细胞。免疫细胞化学结果显示,拉特肌醇B处理减少了基底外侧质膜下区室中的F-肌动蛋白,同时使顶端质膜下区室中的F-肌动蛋白减少并断裂。拉特肌醇B诱导的顶端区域F-肌动蛋白缺失与IP₃R2和IP₃R3的减少同时出现,剩余的IP₃Rs与剩余的F-肌动蛋白定位在一起。蛋白质印迹分析实验表明,IP₃R3s对去污剂提取具有抗性,这表明其与细胞骨架存在潜在相互作用。在全细胞膜片钳记录的细胞中,用拉特肌醇B处理可抑制由肌醇(2,4,5)-三磷酸诱发的Ca²⁺依赖性Cl⁻电流尖峰;这是由于对潜在的局部Ca²⁺信号的抑制。基于这些发现,我们认为IP₃Rs在顶端区域与F-肌动蛋白形成连接,并且这些连接对于局部Ca²⁺尖峰的产生至关重要。