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Unique Morphology and Photoperiodically Regulated Activity of Neurosecretory Canopy Cells in the Pond Snail Lymnaea Stagnalis

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Journal Cell Tissue Res
Date 2023 Jul 7
PMID 37418027
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Abstract

The pond snail Lymnaea stagnalis exhibits clear photoperiodism in egg laying; it lays more eggs in long-day conditions than in medium-day conditions. A key regulator of egg laying is neurosecretory caudo-dorsal cells (CDCs) producing an ovulation hormone in the cerebral ganglia. Paired small budding structures of the cerebral ganglia (viz. the lateral lobe) also promote egg laying in addition to spermatogenesis and maturation of female accessory sex organs. However, it remains unknown which cells in the lateral lobe are responsible for these. Previous anatomical and physiological studies prompted us to hypothesize that canopy cells in the lateral lobe modulate activity of CDCs. However, double labeling of the canopy cell and CDCs revealed no sign of direct neural connections, suggesting that activity of CDCs is regulated either humorally or through a neural pathway independent of canopy cells. In addition, our detailed anatomical re-evaluation confirmed previous observations that the canopy cell bears fine neurites along the ipsilateral axon and extensions from the plasma membrane of the cell body, although the function of these extensions remains unexplored. Furthermore, comparison of electrophysiological properties between long-day and medium-day conditions indicated that the canopy cell's activity is moderately under photoperiodic regulation: resting membrane potentials of long-day snails are shallower than those of medium-day snails, and spontaneously spiking neurons are only observed in long-day conditions. Thus, canopy cells appear to receive photoperiodic information and regulate photoperiod-dependent phenomena, but not provide direct neural inputs to CDCs.

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PMID: 37596422 PMC: 11226556. DOI: 10.1007/s00359-023-01662-6.

References
1.
Andres-Enguix I, Caley A, Yustos R, Schumacher M, Spanu P, Dickinson R . Determinants of the anesthetic sensitivity of two-pore domain acid-sensitive potassium channels: molecular cloning of an anesthetic-activated potassium channel from Lymnaea stagnalis. J Biol Chem. 2007; 282(29):20977-90. DOI: 10.1074/jbc.M610692200. View

2.
Benjamin P, Slade C, Soffe S . The morphology of neurosecretory neurones in the pond snail, Lymnaea stagnalis, by the injection of Procion Yellow and horseradish peroxidase. Philos Trans R Soc Lond B Biol Sci. 1980; 290(1042):449-78. DOI: 10.1098/rstb.1980.0108. View

3.
Brink M, Boer H . An electron microscopical investigation of the follicle gland (cerebral gland) and of some neurosecretory cells in the lateral lobe of the cerebral ganglion of the pulmonate gastropod Lymnaea stagnalis L. Z Zellforsch Mikrosk Anat. 1967; 79(2):230-43. DOI: 10.1007/BF00369287. View

4.
Dardente H, Wood S, Ebling F, Saenz de Miera C . An integrative view of mammalian seasonal neuroendocrinology. J Neuroendocrinol. 2019; 31(5):e12729. DOI: 10.1111/jne.12729. View

5.
de Vlieger T, Kits K, Ter Maat A, Lodder J . Morphology and electrophysiology of the ovulation hormone producing neuro-endocrine cells of the freshwater snail Lymnaea stagnalis (L.). J Exp Biol. 1980; 84:259-71. DOI: 10.1242/jeb.84.1.259. View