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Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes
Published on: September 9, 2020
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Regionalized tissue fluidization is required for epithelial gap closure during insect gastrulation.
Akanksha Jain1,2, Vladimir Ulman1,3, Arghyadip Mukherjee4
1Max-Planck-Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Nature Communications
|November 6, 2020
Summary
Animal embryos close epithelial sheets during epiboly. This study reveals how actomyosin cables drive tissue fluidization at the leading edge, enabling gap closure, a mechanism conserved in wound healing.
Area of Science:
- Developmental Biology
- Cell Biology
- Biophysics
Background:
- Animal embryos undergo epiboly, a gastrulation process involving epithelial sheet closure around the egg.
- The ellipsoidal egg shape necessitates epithelial expansion followed by compaction, creating mechanical stress.
- Releasing mechanical stress is crucial for successful epithelial sheet closure.
Purpose of the Study:
- To investigate the cellular and mechanical mechanisms driving epithelial sheet closure during epiboly.
- To understand how the extraembryonic tissue (serosa) spreads and seals the embryonic surface.
- To identify conserved morphogenetic modules involved in epithelial gap closure.
Main Methods:
- Utilized the insect Tribolium castaneum as a model organism.
- Observed and analyzed cell behavior and tissue dynamics during serosa epiboly.
- Investigated the role of the actomyosin cable in regulating cell intercalation and tissue fluidity.
Main Results:
- The serosa regionalizes into a solid-like dorsal region and a fluid-like ventral region at the leading edge.
- Smaller cells at the ventral leading edge undergo intercalation.
- A heterogeneous actomyosin cable drives cell eviction and intercalation, fluidizing the leading edge.
Conclusions:
- Actomyosin cable-driven tissue fluidization is a key mechanism for epithelial gap closure during epiboly.
- This process shares similarities with wound healing mechanisms.
- Local tissue fluidization represents a conserved morphogenetic module in epithelial closure.
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