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In Vivo Monitoring of Intracellular Chloroplast Movements in Intact Leaves of C_4 Plants Using Two-Photon Microscopy

机译:使用双光子显微镜对C_4植物完整叶片中细胞内叶绿体运动的体内监测

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摘要

Dynamic changes in the spatial distribution of chloroplasts are essential for optimizing photosynthetic capacity under changing light conditions. Light-induced movement of chloroplasts has been widely investigated, but most studies were conducted on isolated tissues or protoplasts. In this study, a two-photon microscopy (TPM) system was adapted to monitor the intracellular 3-dimensional (3D) movements of chloroplasts in intact leaves of plants during dark to light transitions. The TPM imaging was based on autofluorescence of chlorophyll generated by a femto-second Ti:Sapphire laser. All chloroplasts did not exhibit the same motion in response to irradiation variation. In the sub-epidermal mesophyll cells, chloroplasts generally moved away from the surface following blue light treatment, however many chloroplasts did not show any movement. Such spatial heterogeneity in chloroplast motility underlines the importance of monitoring intracellular orientation and movement of individual chloroplasts across intact leaves. Our investigation shows that the 3D imaging of chloroplasts using TPM can help to understand the changes in local photosynthetic capacity in intact leaves under changing environmental conditions.
机译:叶绿体空间分布的动态变化对于在变化的光照条件下优化光合能力至关重要。光诱导的叶绿体运动已得到广泛研究,但是大多数研究是在离体组织或原生质体上进行的。在这项研究中,双光子显微镜(TPM)系统适用于监测植物从完整叶片在黑暗到明亮的过渡过程中叶绿体的细胞内3维(3D)运动。 TPM成像基于飞秒Ti:Sapphire激光器产生的叶绿素自发荧光。响应辐射变化,所有叶绿体均未表现出相同的运动。在表皮下的叶肉细胞中,蓝光处理后,叶绿体通常从表面移开,但是许多叶绿体没有显示任何运动。叶绿体运动性的这种空间异质性强调了监测单个叶绿体跨完整叶片的细胞内方向和运动的重要性。我们的研究表明,使用TPM对叶绿体进行3D成像可以帮助了解在变化的环境条件下完整叶片中局部光合能力的变化。

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