Interface extension is a continuum property suggesting a linkage between AP contractile and DV lengthening processes
Timothy E Vanderleest1, Yi Xie2, Celia Smits2
1Department of Physics and Astronomy, University of Denver, Denver, CO 80208.
Molecular Biology of the Cell
|September 21, 2022
Summary
Cell intercalation in Drosophila embryos involves axis elongation. New dorsal-ventral interfaces elongate via sliding, driven by cell forces and actin networks, not a separate process.
Area of Science:
- Developmental biology
- Cell biology
- Biophysics
Background:
- Axis elongation in early Drosophila embryos relies on cell intercalation.
- This process involves anterior-posterior (AP) interface contraction and dorsal-ventral (DV) interface extension.
- Mechanisms of DV interface elongation are less understood than AP interface contraction.
Purpose of the Study:
- To investigate the mechanisms of new dorsal-ventral (DV) interface elongation during Drosophila germband development.
- To determine if DV interface elongation is a distinct process from AP interface contraction.
Main Methods:
- Live imaging of Drosophila embryos.
- Analysis of cell behaviors, including interface dynamics and vertex formation.
- Investigating the role of cortical F-actin and medial myosin in interface elongation.
Main Results:
- DV interface elongation initiates concurrently with AP interface contraction.
- Newly formed DV interfaces elongate through ratchet-like sliding, similar to AP interfaces.
- Cortical F-actin networks are crucial for the oscillations driving this sliding.
- Medial myosin generates oscillating radial forces, creating asymmetries at tricellular vertices.
Conclusions:
- DV interface elongation is not a separate process but shares mechanisms with AP interface contraction.
- Directional ratcheted sliding, driven by cell forces and planar polarized stabilization, generates both AP contraction and DV elongation.
- This unified mechanism challenges canonical models of axis elongation.
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