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-catenin tyrosine phosphorylation via
Ca2+ during intestinal epithelial cell migration
Departments of 1 Surgery and 2 Pathology, University of Maryland School of Medicine and 3 Baltimore Veterans Affairs Medical Center, Baltimore, Maryland 21201
Polyamines
are essential for early mucosal restitution that occurs by epithelial
cell migration to reseal superficial wounds after injury. Normal
intestinal epithelial cells are tightly bound in sheets, but they need
to be rapidly disassembled during restitution.
-Catenin is involved
in cell-cell adhesion, and its tyrosine phosphorylation causes
disassembly of adhesion junctions, enhancing the spreading of cells.
The current study determined whether polyamines are required for the
stimulation of epithelial cell migration by altering
-catenin
tyrosine phosphorylation. Migration of intestinal epithelial cells
(IEC-6 line) after wounding was associated with an increase in
-catenin tyrosine phosphorylation, which decreased the binding
activity of
-catenin to
-catenin. Polyamine depletion by
-difluoromethylornithine reduced cytoplasmic free Ca2+
concentration ([Ca2+]cyt), prevented
induction of
-catenin phosphorylation, and decreased cell migration.
Elevation of [Ca2+]cyt induced by the
Ca2+ ionophore ionomycin restored
-catenin
phosphorylation and promoted migration in polyamine-deficient cells.
Decreased
-catenin phosphorylation through the tyrosine kinase
inhibitor herbimycin-A or genistein blocked cell migration, which was
accompanied by reorganization of cytoskeletal proteins. These results
indicate that
-catenin tyrosine phosphorylation plays a critical
role in polyamine-dependent cell migration and that polyamines induce
-catenin tyrosine phosphorylation at least partially through
[Ca2+]cyt.
ornithine decarboxylase; cell adhesion; tyrosine kinase;
-catenin; intracellular calcium; restitution; intestinal epithelial
cells
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