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High-resolution confocal imaging of wall ingrowth deposition in plant transfer cells: Semi-quantitative analysis of phloem parenchyma transfer cell development in leaf minor veins of Arabidopsis

机译:植物转移细胞壁向内生长的高分辨率共聚焦成像:拟南芥叶片次要静脉韧皮部实质转移细胞发育的半定量分析

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摘要

BackgroundTransfer cells (TCs) are trans-differentiated versions of existing cell types designed to facilitate enhanced membrane transport of nutrients at symplasmic/apoplasmic interfaces. This transport capacity is conferred by intricate wall ingrowths deposited secondarily on the inner face of the primary cell wall, hence promoting the potential trans-membrane flux of solutes and consequently assigning TCs as having key roles in plant growth and productivity. However, TCs are typically positioned deep within tissues and have been studied mostly by electron microscopy.Recent advances in fluorophore labelling of plant cell walls using a modified pseudo-Schiff-propidium iodide (mPS-PI) staining procedure in combination with high-resolution confocal microscopy have allowed visualization of cellular details of individual tissue layers in whole mounts, hence enabling study of tissue and cellular architecture without the need for tissue sectioning. Here we apply a simplified version of the mPS-PI procedure for confocal imaging of cellulose-enriched wall ingrowths in vascular TCs at the whole tissue level.
机译:背景转移细胞(TC)是现有细胞类型的转分化形式,旨在促进营养在同质/无质界面上的膜转运。继而沉积在原代细胞壁内表面上的复杂壁向内生长赋予了这种运输能力,因此促进了潜在的跨膜溶质通量,因此将TC归因于植物生长和生产力中的关键作用。然而,TCs通常位于组织内部深处,并且已经通过电子显微镜进行了研究。使用改良的伪希夫-碘化丙啶(mPS-PI)染色方法结合高分辨率共聚焦技术在植物细胞壁的荧光团标记上的最新进展显微镜使整个组织中各个组织层的细胞细节可视化,因此无需组织切片即可研究组织和细胞结构。在这里,我们对整个组织水平的血管TC中富含纤维素的壁向内生长的共聚焦成像应用了mPS-PI程序的简化版本。

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