Plant Gene Expression Center, United States Department of Agriculture/Agricultural Research Service, Albany, California 94710, USA.
Plant Physiol. 2010 Apr;152(4):2200-10. doi: 10.1104/pp.109.142349. Epub 2010 Feb 24.
During polarized growth of pollen tubes, endomembrane trafficking and actin polymerization are two critical processes that establish membrane/wall homeostasis and maintain growth polarity. Fine-tuned interactions between these two processes are therefore necessary but poorly understood. To better understand such cross talk in the model plant Arabidopsis (Arabidopsis thaliana), we first established optimized concentrations of drugs that interfere with either endomembrane trafficking or the actin cytoskeleton, then examined pollen tube growth using fluorescent protein markers that label transport vesicles, endosomes, or the actin cytoskeleton. Both brefeldin A (BFA) and wortmannin disturbed the motility and structural integrity of ARA7- but not ARA6-labeled endosomes, suggesting heterogeneity of the endosomal populations. Disrupting endomembrane trafficking by BFA or wortmannin perturbed actin polymerization at the apical region but not in the longitudinal actin cables in the shank. The interference of BFA/wortmannin with actin polymerization was progressive rather than rapid, suggesting an indirect effect, possibly due to perturbed endomembrane trafficking of certain membrane-localized signaling proteins. Both the actin depolymerization drug latrunculin B and the actin stabilization drug jasplakinolide rapidly disrupted transport of secretory vesicles, but each drug caused distinct responses on different endosomal populations labeled by ARA6 or ARA7, indicating that a dynamic actin cytoskeleton was critical for some steps in endomembrane trafficking. Our results provide evidence of cross talk between endomembrane trafficking and the actin cytoskeleton in pollen tubes.
在花粉管的极化生长过程中,内膜运输和肌动蛋白聚合是建立膜/壁动态平衡和维持生长极性的两个关键过程。因此,这两个过程之间的精细相互作用是必要的,但了解甚少。为了更好地理解拟南芥(Arabidopsis thaliana)这一模式植物中的这种交流,我们首先建立了干扰内膜运输或肌动蛋白细胞骨架的药物的优化浓度,然后使用标记运输囊泡、内体或肌动蛋白细胞骨架的荧光蛋白标记物来检查花粉管的生长。布雷菲德菌素 A(BFA)和渥曼青霉素都干扰了 ARA7-但不干扰 ARA6 标记的内体的运动和结构完整性,这表明内体群体存在异质性。BFA 或渥曼青霉素破坏内膜运输扰乱了顶端区域的肌动蛋白聚合,但在柄部的纵向肌动蛋白缆索中没有。BFA/渥曼青霉素对肌动蛋白聚合的干扰是渐进的而不是快速的,这表明存在间接效应,可能是由于某些定位于膜的信号蛋白的内膜运输受到干扰。肌动蛋白解聚药物 latrunculin B 和肌动蛋白稳定药物 jasplakinolide 都迅速破坏了分泌囊泡的运输,但每种药物对 ARA6 或 ARA7 标记的不同内体群体都引起了不同的反应,这表明动态肌动蛋白细胞骨架对内膜运输的某些步骤至关重要。我们的结果提供了花粉管中内膜运输和肌动蛋白细胞骨架之间存在交流的证据。