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ZO-1 shuttles between apical junctional complexes and podosomes by riding ERK activation waves
Sayuki Hirano1,2,3,4,5, Yohei Kondo6,7,8,9,10, Asayuki Kitajima6
1Laboratory of Quantitative Biology, Graduate School of Biostudies, Kyoto University, Kyoto, Japan. hirano.sayuki.2k@kyoto-u.ac.jp.
Nature Communications
|May 9, 2026
Summary
Zonula occludens-1 (ZO-1) protein moves to cell-matrix adhesions, promoting invasive migration and coordinating collective cell movement. This reveals ZO-1
Area of Science:
- Cell Biology
- Molecular Biology
- Biophysics
Background:
- Collective cell migration is crucial for development and disease, but coordination mechanisms are unclear.
- Zonula occludens-1 (ZO-1) is a tight junction protein, traditionally linked to cell-cell adhesion.
Purpose of the Study:
- To investigate the role of ZO-1 in collective cell migration.
- To understand how ZO-1 influences cell-extracellular matrix interactions during migration.
Main Methods:
- Immunofluorescence microscopy to track ZO-1 localization.
- Biochemical assays to assess protein interactions and signaling pathways.
- Cell migration assays to quantify migratory behavior.
Main Results:
- ZO-1 dynamically translocates from tight junctions to cell-extracellular matrix adhesion sites (podosomes) during migration.
- Extracellular signal-regulated kinase (ERK) activation triggers ZO-1 translocation to podosomes.
- ZO-1 at podosomes promotes invasive migration and influences collective cell migration dynamics.
Conclusions:
- ZO-1 plays a novel dual role in collective cell migration, regulating both cell-ECM interactions and intercellular signaling.
- ZO-1 acts as a key integrator of individual cell behavior into coordinated collective movement.
- Targeting ZO-1 function may offer therapeutic strategies for diseases involving aberrant cell migration.
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