Fig. 6.
-actinin changes the organization of both the F-actin and the
cytokeratin network. Low magnification (left panels) and high magnification
(right panels) double-label confocal micrographs showing F-actin (red) and
cytokeratin (green) in rapidly frozen extract samples prepared after the
addition of
-actinin. The exogenous
-actinin results in fine,
highly crosslinked meshworks of F-actin cables in extracts that colocalize
with cytokeratin. At high magnification, cytokeratin localization along
F-actin cables in these networks appears punctate. The bar graph shows that
the addition of exogenous
-actinin significantly decreased the mean
distance between both adjacent F-actin cables and cytokeratin relative to
control samples (P<0.05).