Abstract
In plants, the partitioning of daughter cells during cytokinesis is achieved via physical insertion of a membranous cell plate within the dividing parent cell. It is a cellular process of extensive protein secretion and membrane trafficking toward the plane of cell division and the cytoskeleton is an important facilitator of this process. A specialized cytoskeletal array termed phragmoplast expands centrifugally throughout cytokinesis and directs, mostly Golgi-derived vesicles that ultimately fuse to form the developing cell plate. The function of the phragmoplast in guiding cell plate synthesis has strongly motivated many scientists to monitor its dynamic behavior. In this chapter, we present an overview of basic principles and methods concerning the live imaging of cytokinetic plant cells using confocal laser scanning microscopy (CLSM) and the analysis of phragmoplast expansion.
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Acknowledgments
Research in the laboratory of S.M. is provided by the Deutsche Forschungsgemeinschaft (grants MU3133/1-1, MU3133/3-1 and SFB1101).
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Livanos, P., Chugh, M., Müller, S. (2017). Analysis of Phragmoplast Kinetics During Plant Cytokinesis. In: Jiang, L. (eds) Plant Protein Secretion. Methods in Molecular Biology, vol 1662. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7262-3_12
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DOI: https://doi.org/10.1007/978-1-4939-7262-3_12
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