Abstract
Type I serous glands in the skin of the Eastern yellow-bellied toad Bombina orientalis released their product massively after 10-3 M nor-adrenalin (NA) stimulation, mimicking orthosympathetic control on poison emission in chemical skin defence. Features of cutaneous glands involved in this bulk discharge were observed under light and electron microscopes. Furthermore, restoration of depleted glands was followed after 1, 2 and 3 weeks, and compared with serous biosynthesis during larval gland development. Bulk discharge was caused by contraction of myoepithelial cells (mecs) encircling the secretory units. Mec compression dramatically affected the secretory unit, but parts of this syncytial cytoplasm were saved from degeneration and cooperated in gland renewal with stem cells from the gland neck. These adenoblasts underwent proliferation and secretory cytodifferentiation, until merging with the syncytium. Cytoplasm that had resumed secretory activity showed the features typical of larval gland development: the endoplasmic reticulum (rer) cisterns were aligned in close parallel arrangement and Golgi stacks released minute type I granules. Secretory rehabilitation led to increasing amounts of granule content. In the meantime, rough cisterns decreased in number and assumed the less ordered pattern described in control specimens. Data collected in the present study revealed that chemical skin defence in anurans is a multi-factorial mechanism involving specific activities: mechanical from mecs, biosynthetic from secretory syncytium and proliferative from intercalated stem cells.
