Live Leaf-Section Imaging for Visualizing Intracellular Chloroplast Movement and Analyzing Cell-Cell Interactions.

IF 1.1 Q3 BIOLOGY
Yuta Kato, Takao Oi, Yoshikatsu Sato, Mitsutaka Taniguchi
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Abstract

In response to environmental changes, chloroplasts, the cellular organelles responsible for photosynthesis, undergo intracellular repositioning, a phenomenon known as chloroplast movement. Observing chloroplast movement within leaf tissues remains technically challenging in leaves consisting of multiple cell layers, where light scattering and absorption hinder deep tissue visualization. This limitation has been particularly problematic when analyzing chloroplast movement in the mesophyll cells of C4 plants, which possess two distinct types of concentrically arranged photosynthetic cells. In response to stress stimuli, mesophyll chloroplasts aggregate toward the inner bundle sheath cells. However, conventional methods have not been able to observe these chloroplast dynamics over time in living cells, making it difficult to assess the influence of adjacent bundle sheath cells on this movement. Here, we present a protocol for live leaf section imaging that enables long-term and detailed observation of chloroplast movement in internal leaf tissues without chemical fixation. In this method, a leaf blade section prepared either using a vibratome or by hand was placed in a groove made of a silicone rubber sheet attached to a glass slide for microscopic observation. This technique allows for the quantitative tracking of chloroplast movement relative to the surrounding cells. In addition, by adjusting the sectioning angle and thickness of the unfixed leaf sections, it is possible to selectively inactivate specific cell types based on their size and shape differences. This protocol enables the investigation of the intercellular interactions involved in chloroplast dynamics in leaf tissues. Key features • Thin leaf sections prepared while still alive enable prolonged microscopic observation of chloroplast movement within the leaf tissue. • Selective cell inactivation can be achieved by adjusting the slice thickness and angle. • This method is applicable to a wide range of plant species.

活叶切片成像用于观察胞内叶绿体运动和分析细胞-细胞相互作用。
作为对环境变化的响应,负责光合作用的细胞器叶绿体在细胞内进行重新定位,这种现象被称为叶绿体运动。观察叶片组织中的叶绿体运动在技术上仍然具有挑战性,因为叶片由多个细胞层组成,其中光散射和吸收阻碍了深层组织的可视化。当分析C4植物叶肉细胞中的叶绿体运动时,这种限制尤其成问题,C4植物具有两种不同类型的同心排列的光合细胞。叶肉叶绿体在应激刺激下向内束鞘细胞聚集。然而,传统的方法无法在活细胞中观察这些叶绿体随时间的动态,因此很难评估相邻束鞘细胞对这种运动的影响。在这里,我们提出了一种活体叶片切片成像方案,可以在没有化学固定的情况下长期和详细地观察叶片内部组织中的叶绿体运动。在这种方法中,使用振动器或手工制备的叶片切片被放置在附着在玻璃载玻片上的硅橡胶片制成的凹槽中进行显微镜观察。这种技术允许对叶绿体相对于周围细胞的运动进行定量跟踪。此外,通过调整未固定叶片切片的切片角度和厚度,可以根据细胞的大小和形状差异选择性地灭活特定类型的细胞。该协议使研究参与叶片组织叶绿体动力学的细胞间相互作用成为可能。•在叶片组织中制备的薄叶切片可以对叶绿体运动进行长时间的显微观察。•可通过调整切片厚度和角度实现选择性细胞失活。•这种方法适用于多种植物物种。
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CiteScore
1.50
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