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PreprintCC0arXiv

Full Three-dimensional Cell Geometry Matters for Epithelial Fluidization

Abstract

Epithelial dynamics are often studied using two-dimensional models that omit cell height. Here, we investigate how this third dimension influences tissue fluidization driven by cell self-propulsion. We identify three effects absent from conventional 2D models. First, cell height controls fluidization through a reentrant transition: squamous and columnar tissues are more resistant to fluidization than cuboidal ones. Second, neighbor exchanges through transient scutoid states substantially enhance cell motility, compared to classic T1 transitions. Third, self-propelling cells develop pronounced apicobasal shape asymmetry, with the experimentally less accessible basal surface providing a more accurate indicator of cells' target shape index and motility.

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BibTeX
@misc{chiba2026full,
  title = {{Full Three-dimensional Cell Geometry Matters for Epithelial Fluidization}},
  author = {Toshikaze Chiba and Jan Rozman and Matej Krajnc},
  howpublished = {arXiv},
  year = {2026},
  month = oct,
  doi = {10.48550/arxiv.2610.20030},
  eprint = {2610.20030},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2610.20030},
  note = {CC0},
}
RIS
TY  - UNPB
TI  - Full Three-dimensional Cell Geometry Matters for Epithelial Fluidization
AU  - Toshikaze Chiba
AU  - Jan Rozman
AU  - Matej Krajnc
PY  - 2026
DA  - 2026/10/14
PB  - arXiv
DO  - 10.48550/arxiv.2610.20030
UR  - https://arxiv.org/abs/2610.20030
AB  - Epithelial dynamics are often studied using two-dimensional models that omit cell height. Here, we investigate how this third dimension influences tissue fluidization driven by cell self-propulsion. We identify three effects absent from conventional 2D models. First, cell height controls fluidization through a reentrant transition: squamous and columnar tissues are more resistant to fluidization than cuboidal ones. Second, neighbor exchanges through transient scutoid states substantially enhance cell motility, compared to classic T1 transitions. Third, self-propelling cells develop pronounced apicobasal shape asymmetry, with the experimentally less accessible basal surface providing a more accurate indicator of cells' target shape index and motility.
ER  -