Ew. Roubos et Wra. Vanheumen, PEPTIDE PROCESSING AND RELEASE BY THE NEUROENDOCRINE CAUDODORSAL CELLS OF LYMNAEA-STAGNALIS DURING AN EGG-LAYING CYCLE, Brain research, 644(1), 1994, pp. 83-89
The freshwater mollusc Lymnaea stagnalis exhibits an egg-laying cycle
that takes about 24 h. The cycle is under control of the cerebral neur
oendocrine Caudodorsal Cells (CDC), which release various peptides, on
e of which is the ovulation-inducing hormone, CDCH. During the egg-lay
ing cycle the CDC reveal three consecutive states of electrical activi
ty, the resting, the active and the inhibited state. Processing and re
lease of CDCH have been studied in relation to the states of electrica
l (and secretory) activity of the CDC, with quantitative immuno-electr
on microscopy and a newly raised CDCH antiserum. In somata of CDC in t
he resting state 1 (just before activation of the CDC), in the active
state (30 min after activation) and in the inhibited state (3 h after
activation) more secretory granules are immunolabelled, and to a highe
r degree, than in somata of CDC in the resting state 2 (10 h after act
ivation). Axon terminals of CDC in resting states 1 and 2 are equally
immunoreactive, whereas in terminals in the active state more granules
are labelled, and to a higher degree, than in the resting states. Sec
retory granules in terminals in the inhibited state are intermediate i
n both respects. Immune-electron microscopy combined with the tannic a
cid method for the demonstration of exocytosis showed that in terminal
s in the active state, the percentage of immunolabelled exocytosed gra
nule contents is much higher than in the other states. The same holds
for the degree of immunopositivity of these contents. It is proposed t
hat the activity of the CDC depends on their state of electrical and s
ecretory activity, not only with respect to the rate of CDCH release (
maximal in active state) but also with regard to the rate of precursor
processing (maximal in resting state 2) and posttranslational modific
ation of CDCH within secretory granules in the neurohemal axon termina
ls (maximal in active state).