Skip to Content
Merck

The nature of cell division forces in epithelial monolayers.

The Journal of cell biology (2021-06-17)
Vivek K Gupta, Sungmin Nam, Donghyun Yim, Jaclyn Camuglia, Judy Lisette Martin, Erin Nicole Sanders, Lucy Erin O'Brien, Adam C Martin, Taeyoon Kim, Ovijit Chaudhuri
ABSTRACT

Epithelial cells undergo striking morphological changes during division to ensure proper segregation of genetic and cytoplasmic materials. These morphological changes occur despite dividing cells being mechanically restricted by neighboring cells, indicating the need for extracellular force generation. Beyond driving cell division itself, forces associated with division have been implicated in tissue-scale processes, including development, tissue growth, migration, and epidermal stratification. While forces generated by mitotic rounding are well understood, forces generated after rounding remain unknown. Here, we identify two distinct stages of division force generation that follow rounding: (1) Protrusive forces along the division axis that drive division elongation, and (2) outward forces that facilitate postdivision spreading. Cytokinetic ring contraction of the dividing cell, but not activity of neighboring cells, generates extracellular forces that propel division elongation and contribute to chromosome segregation. Forces from division elongation are observed in epithelia across many model organisms. Thus, division elongation forces represent a universal mechanism that powers cell division in confining epithelia.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Monoclonal Anti-Uvomorulin/E-Cadherin antibody produced in rat, clone DECMA-1, ascites fluid, buffered aqueous solution
Sigma-Aldrich
DAPI, for nucleic acid staining
Roche
cOmplete ULTRA Tablets, Mini, EDTA-free, EASYpack Protease Inhibitor Cocktail, Tablets supplied in foil blister packs.
SAFC
Insulin, Human Recombinant, for research or for further manufacturing use, dry powder
Sigma-Aldrich
Blebbistatin, Racemic, InSolution, ≥97%, 50 mM in 90% DMSO, reversible inhibitor of nonmuscle myosin II
Sigma-Aldrich
Hydrocortisone, BioReagent, suitable for cell culture
Sigma-Aldrich
Cholera Toxin from Vibrio cholerae, ≥90% (SDS-PAGE), lyophilized powder
Sigma-Aldrich
BTO-1, ≥98% (HPLC), solid