Focal adhesion kinase signaling is decreased in polyamine-depleted IEC-6 cells

Polyamines are essential to the migration ofepithelial cells in the intestinal mucosa. Cells depleted of polyaminesdo not attach as rapidly to the extracellular matrix and do not form the actin stress fibers essential for migration. Because both attachment and stress fiber formation depend on integrin signaling andthe formation of focal adhesions, we examined these and related processes in polyamine-depleted IEC-6 cells. There was general decreased tyrosine phosphorylation of focal adhesion kinase (FAK), and,specifically, decreased phosphorylation of Tyr-925, the paxillin binding site. In control cells, FAK phosphorylation was rapid afterattachment to the extracellular matrix, while attached cells depletedof polyamines had significantly delayed phosphorylation. FAK activitywas also significantly inhibited in polyamine-depleted cells as was thephosphorylation of paxillin. Polyamine-depleted cells failed to spreadnormally after attachment, and immunocytochemistry showed littlecolocalization of FAK and actin compared with controls. Focal adhesioncomplex formation was greatly reduced in the absence of polyamines.These data suggest that defective integrin signaling may, at least inpart, account for the decreased rates of attachment, actin stress fiberformation, spreading, and migration observed in polyamine-depleted cells.