Phragmoplast

The phragmoplast is a plant-cell structure that coordinates cytokinesis, the final stage of cell division, by positioning the new cell wall between daughter cells. It forms from overlapping microtubules, actin filaments, and associated proteins at the division plane, while Golgi-derived vesicles move along these cytoskeletal tracks, fuse at the center, and build a cell plate that expands outward until it connects with the existing cell wall. Studying the phragmoplast reveals how plant cells establish tissue architecture, maintain cellular boundaries, and divide accurately, with relevance to plant development, growth, and responses to environmental conditions.

Phragmoplast - Related Videos

Education

JoVE Core - Cell Biology

The Phragmoplast

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2023

Cell division is essential for organismal growth and development. In animal cells, the central spindle and its associated proteins form the midbody, a structure that has an essential role in cytokinesis. In plants, the central spindle, along with the microtubules, actin, and other cell components, matures into the phragmoplast, which is necessary for cytokinesis. Unlike the stationary midbody, the phragmoplast expands centrifugally, eventually leading to the formation of the new cell wall. The...

The Phragmoplast

0 Views •

2021

Cell division is essential for organismal growth and development. In animal cells, the central spindle and its associated proteins form the midbody, a structure that has an essential role in cytokinesis. In plants, the central spindle, along with the microtubules, actin, and other cell components, matures into the phragmoplast, which is necessary for cytokinesis. Unlike the stationary midbody, the phragmoplast expands centrifugally, eventually leading to the formation of the new cell wall. The...

Research

JoVE Journal - Developmental Biology
Free Sample

A Simple Chamber for Long-term Confocal Imaging of Root and Hypocotyl Development

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Cited by 25 •

2017

Presented here is a simple technique for high-resolution confocal time-lapse imaging of root and hypocotyl development for up to 3 days using high numerical-aperture objectives and perfluorodecalin as an immersion medium.

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