PUBLICATION

Live imaging in zebrafish reveals tissue-specific strategies for amoeboid migration

Authors
Robertson, T.F., Schrope, J., Zwick, Z., Rindy, J., Horn, A., Hou, Y., Huttenlocher, A.
ID
ZDB-PUB-250322-6
Date
2025
Source
Development (Cambridge, England) : (Journal)
Registered Authors
Huttenlocher, Anna
Keywords
Actin, Bleb, Cell migration, T cells, Tissues, Zebrafish
MeSH Terms
  • Actins/metabolism
  • Animals
  • Cell Movement*/physiology
  • Epidermis/metabolism
  • Keratinocytes/cytology
  • Keratinocytes/metabolism
  • Organ Specificity
  • Pseudopodia/metabolism
  • T-Lymphocytes*/cytology
  • T-Lymphocytes*/physiology
  • Zebrafish*/embryology
PubMed
40114648 Full text @ Development
Abstract
Amoeboid cells like leukocytes can enter and migrate in diverse tissues, even though tissues vary widely in their chemical and mechanical composition. Here, we imaged motile T cells as they colonized peripheral tissues during zebrafish development to ask if cells tailor their migration strategy to their local tissue environment. We found that T cells in most sites migrated with F-actin-rich leading-edge pseudopods, matching how they migrate in vitro. T cells notably deviated from this strategy in the epidermis, where they instead migrated using a rearward concentration of F-actin and stable leading-edge blebs. This mode of migration occurs under planar confinement in vitro, and we found the stratified keratinocyte layers of the epidermis also impose planar-like confinement on leukocytes in vivo. Collectively, our data indicate that immune cells adapt their migration strategy to navigate different tissue geometries in vivo.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping