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Methods Cell Biol. 2017;137:73-84. doi: 10.1016/bs.mcb.2016.04.013. Epub 2016 Jun 11.

Studying cytokinesis in Drosophila epithelial tissues.

Author information

1
Institut Curie, PSL Research University, Paris, France; Sorbonne Universités, Paris, France; Abel Salazar Biomedical Sciences Institute, University of Porto, Porto, Portugal.
2
Institut Curie, PSL Research University, Paris, France; Sorbonne Universités, Paris, France.

Abstract

Epithelial tissue cohesiveness is ensured through cell-cell junctions that maintain both adhesion and mechanical coupling between neighboring cells. During development, epithelial tissues undergo intensive cell proliferation. Cell division, and particularly cytokinesis, is coupled to the formation of new adhesive contacts, thereby preserving tissue integrity and propagating cell polarity. Remarkably, the geometry of the new interfaces is determined by the combined action of the dividing cell and its neighbors. To further understand the interplay between the dividing cell and its neighbors, as well as the role of cell division for tissue morphogenesis, it is important to analyze cytokinesis in vivo. Here we present methods to perform live imaging of cell division in Drosophila epithelial tissues and discuss some aspects of image processing and analysis.

KEYWORDS:

Confocal time-lapse imaging; Cytokinesis; Epithelial tissues; Mechanics

PMID:
28065321
DOI:
10.1016/bs.mcb.2016.04.013
[Indexed for MEDLINE]

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