Martens Helle Juel, Gao Chen, Liesche Johannes
Department of Geosciences and Natural Resources, University of Copenhagen, Copenhagen, Denmark.
College of Life Sciences, Northwest A&F University, Yangling, China.
Methods Mol Biol. 2019;2014:215-221. doi: 10.1007/978-1-4939-9562-2_18.
Sugars produced by photosynthesis in leaves get transported to other organs in the phloem vascular tissue. Three general mechanisms have been proposed for the loading of sugars into the phloem. These differ in the involvement of active transport across the phloem cell's membrane and their capacity for passive intercellular transport through plasmodesmata. This capacity for diffusion from the mesophyll into the phloem cells can be quantified by live-cell microscopy. Instead of sugar molecules, the movement of fluorescent tracers of similar size can be observed. In this chapter, a simple method is described that allows quantification of plasmodesmata-mediated intercellular diffusion across the mesophyll-bundle sheath interface and the bundle sheath-phloem cell interfaces. The fluorescent tracer carboxyfluorescein is loaded into intact leaves and its diffusion monitored with confocal microscopy after photobleaching of a bundle sheath cell.
叶片通过光合作用产生的糖类通过韧皮部维管组织运输到其他器官。关于糖类加载到韧皮部,已提出三种一般机制。这些机制在跨韧皮部细胞膜的主动运输参与情况以及通过胞间连丝进行被动细胞间运输的能力方面存在差异。这种从中叶扩散到韧皮部细胞的能力可以通过活细胞显微镜进行量化。可以观察到的不是糖分子,而是类似大小的荧光示踪剂的移动。在本章中,描述了一种简单的方法,该方法可以量化胞间连丝介导的跨叶肉-维管束鞘界面和维管束鞘-韧皮部细胞界面的细胞间扩散。将荧光示踪剂羧基荧光素加载到完整叶片中,并在对一个维管束鞘细胞进行光漂白后用共聚焦显微镜监测其扩散。