Wang Qinli, Kong Lingan, Hao Huaiqing, Wang Xiaohua, Lin Jinxing, Samaj Jozef, Baluska Frantisek
Key Laboratory of Photosynthesis and Molecular Environment Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Plant Physiol. 2005 Dec;139(4):1692-703. doi: 10.1104/pp.105.069765. Epub 2005 Nov 18.
We assessed the effects of brefeldin A (BFA) on pollen tube development in Picea meyeri using fluorescent marker FM4-64 as a membrane-inserted endocytic/recycling marker, together with ultrastructural studies and Fourier transform infrared analysis of cell walls. BFA inhibited pollen germination and pollen tube growth, causing morphological changes in a dose-dependent manner, and pollen tube tip growth recovered after transferring into BFA-free medium. FM4-64 labeling showed typical bright apical staining in normally growing P. meyeri pollen tubes; this apical staining pattern differed from the V-formation pattern found in angiosperm pollen tubes. Confocal microscopy revealed that exocytosis was greatly inhibited in the presence of BFA. In contrast, the overall uptake of FM4-64 dye was about 2-fold that in the control after BFA (5 microg mL(-1)) treatment, revealing that BFA stimulated endocytosis in a manner opposite to the induced changes in exocytosis. Transmission electron microscopic observation showed that the number of secretory vesicles at the apical zone dramatically decreased, together with the disappearance of paramural bodies, while the number of vacuoles and other larger organelles increased. An acid phosphatase assay confirmed that the addition of BFA significantly inhibited secretory pathways. Importantly, Fourier transform infrared microspectroscopy documented significant changes in the cell wall composition of pollen tubes growing in the presence of BFA. These results suggest that enhanced endocytosis, together with inhibited secretion, is responsible for the retarded growth of pollen tubes induced by BFA.
我们使用荧光标记物FM4-64作为膜插入的内吞/再循环标记物,结合超微结构研究和细胞壁的傅里叶变换红外分析,评估了布雷菲德菌素A(BFA)对白杄花粉管发育的影响。BFA抑制花粉萌发和花粉管生长,以剂量依赖的方式引起形态变化,并且在转移到不含BFA的培养基后花粉管顶端生长恢复。FM4-64标记在正常生长的白杄花粉管中显示出典型的明亮顶端染色;这种顶端染色模式不同于被子植物花粉管中发现的V形模式。共聚焦显微镜显示,在BFA存在下胞吐作用受到极大抑制。相反,BFA(5μg mL(-1))处理后,FM4-64染料的总体摄取量约为对照的2倍,表明BFA以与胞吐作用诱导变化相反的方式刺激内吞作用。透射电子显微镜观察表明,顶端区域分泌小泡的数量显著减少,同时壁旁体消失,而液泡和其他较大细胞器的数量增加。酸性磷酸酶测定证实,添加BFA显著抑制分泌途径。重要的是,傅里叶变换红外显微光谱记录了在BFA存在下生长的花粉管细胞壁组成的显著变化。这些结果表明,内吞作用增强以及分泌受到抑制是BFA诱导花粉管生长迟缓的原因。