PEPTIDE PROCESSING AND RELEASE BY THE NEUROENDOCRINE CAUDODORSAL CELLS OF LYMNAEA-STAGNALIS DURING AN EGG-LAYING CYCLE

Citation
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
Citations number
17
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00068993
Volume
644
Issue
1
Year of publication
1994
Pages
83 - 89
Database
ISI
SICI code
0006-8993(1994)644:1<83:PPARBT>2.0.ZU;2-M
Abstract
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).