Closterium acerosum possesses a well-defined, mucilage-secretory mechanism
consisting of up to 100 Golgi bodies, two distinct vacuolar networks, and a
n active cytoplasmic-streaming network located in the cell periphery. Five
different sodium-affecting agents were applied to actively secreting cells
in order to determine the role, if any, of Na+ on this secretory mechanism.
Significant effects to the endomembrane system and actin cytoskeleton were
noted upon treatment with the Na+-specific ionophores monensin and SQ1-Et.
In particular, the following alterations were noted: incurling of Golgi ci
sternae and the formation of circular cisternal profiles at the trans face,
swelling of the cis-medial cisternae, and dissociation of the Golgi body f
rom the internal cytoplasm to the peripheral cytoplasmic zones. Immunogold
labeling with a mucilage-specific polyclonal antibody reveals that mucilage
production is diminished during longer ionophore treatments. Likewise, bot
h the polar and peripheral vacuoles disintegrate into a series of smaller v
acuoles. Cytoplasmic streaming ceases and the normal actin network of the p
eripheral cytoplasm transforms into irregularly spaced fibrillar bundles. F
inally, multilaminate structures appear at the plasma membrane. No cytologi
cal effects could be observed with the Na+-channel blockers or Na+-current
transducers QX-14, tetrodotoxin, or amiloride.