Tan Toh Weng, Pfau Bastian, Jones David, Meyer Thomas
Institute for Experimental Orthopaedics and Biomechanics, University of Marburg, Marburg, Germany.
J Mol Histol. 2014 Feb;45(1):81-9. doi: 10.1007/s10735-013-9530-7. Epub 2013 Aug 10.
Adenosine 5'-triphosphate (ATP), released in response to mechanical and inflammatory stimuli, induces the dynamic and asynchronous protrusion and subsequent retraction of local membrane structures in osteoblasts. The molecular mechanisms involved in the ligand-stimulated herniation of the plasma membrane are largely unknown, which prompted us to investigate whether the focal-adhesion protein vinculin is engaged in the cytoskeletal alterations that underlie the ATP-induced membrane blebbing. Using time-lapse fluorescence microscopy of primary bovine osteoblast-like cells expressing green fluorescent protein-tagged vinculin, we found that stimulation of cells with 100 μM ATP resulted in the transient and rapid clustering of recombinant vinculin in the cell periphery, starting approximately 100 s after addition of the nucleotide. The ephemeral nature of the vinculin clusters was made evident by the brevity of their mean assembly and disassembly times (66.7 ± 13.3 s and 99.0 ± 6.6 s, respectively). Traction force vector maps demonstrated that the vinculin-rich clusters were localized predominantly at sites of high traction force. Intracellular calcium measurements showed that the ligand-induced increase in [Ca(2+)]i clearly preceded the clustering of vinculin, since [Ca(2+)]i levels returned to normal within 30 s of exposure to ATP, indicating that intracellular calcium transients trigger a cascade of signalling events that ultimately result in the incorporation of vinculin into membrane-associated focal aggregates.
腺苷5'-三磷酸(ATP)在受到机械和炎症刺激时释放,可诱导成骨细胞中局部膜结构的动态和异步突出及随后的回缩。质膜受配体刺激后突出的分子机制在很大程度上尚不清楚,这促使我们研究粘着斑蛋白纽蛋白是否参与了ATP诱导的膜泡形成所依赖的细胞骨架改变。通过对表达绿色荧光蛋白标记纽蛋白的原代牛成骨样细胞进行延时荧光显微镜观察,我们发现用100μM ATP刺激细胞后,重组纽蛋白在细胞周边短暂快速聚集,在添加核苷酸后约100秒开始。纽蛋白簇的短暂性质通过其平均组装和拆卸时间的短暂得以体现(分别为66.7±13.3秒和99.0±6.6秒)。牵引力矢量图显示,富含纽蛋白的簇主要位于高牵引力部位。细胞内钙测量表明,配体诱导的[Ca(2+)]i增加明显先于纽蛋白的聚集,因为在暴露于ATP后30秒内[Ca(2+)]i水平恢复正常,这表明细胞内钙瞬变触发了一系列信号事件,最终导致纽蛋白整合到与膜相关的粘着聚集体中。