| Literature DB >> 28861824 |
Pantelis Livanos1, Mayank Chugh2, Sabine Müller3.
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.Keywords: Arabidopsis; CLSM; Cell plate; Cytokinesis; FM4-64; GFP; MAP4; MBD; Microtubules; Phragmoplast
Mesh:
Substances:
Year: 2017 PMID: 28861824 DOI: 10.1007/978-1-4939-7262-3_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745