Literature DB >> 8798

The anatomy of neurosecretory neurones in the pond snail Lymnaea stagnalis (L.).

N V Swindale, P R Benjamin.   

Abstract

The anatomy of three neurosecretory cell types in the central nervous system (c.n.s.) of the gastropod mollusc Lymnaea stagnalis (L.)- the Dark Green Cells, Yellow Cells and Yellow-green Cells-has been studied by using bright and dark field illumination of material stained for neurosecretion by the Alcian Blue-Alcian Yellow technique. The neuronal geometry of single and groups of neurosecretory cells of the various types has been reconstructed from serial sections, and the likely destination of most of their processes has been determined. Dark Green Cells are monopolar, occur exclusively within the central nervous system (c.n.s.), have few or no branches terminating in neuropile, and send axons to the surface of the pleuro-parietal and pleuro-cerebral connectives. The majority of Dark Green Cell axons however (80-85%), project down nerves which innervate ventral and anterior parts of the head-foot, the neck and the mantle. Dark Green Cell axons can be found in small nerves throughout these areas, and may terminate in a find plexus of axons on the surfaces of the nerves. Since previous experimental work has shown that the Dark Green Cells are involved in osmotic or ionic regulation, these results suggest that the target organ of the Dark Green Cells may be the skin. Yellow Cells occur both within and outside the c.n.s. They are usually monopolar, but can be bipolar. They have several axons which normally arise separately from a single pole of the cell body, or close to it. One or more processes leave the cell proximal to the point where separate axons arise, and may run unbranched for some distance through neuropile before terminating in fine brances and blobs of various sizes. These branches may release hormone inside the c.n.s. Yellow-green Cells are mono-, bi- or multi-polar, and like the Yellow Cells are found both within and outside the c.n.s. Some Yellow-green Cells, though not all, have projections which terminate in neuropile in fine branches and blobs. Yellow-green Cell bodies which occur in nerves can project back along the nerve into the c.n.s. The axons of Yellow Cells and Yellow-green Cells project to release sites in various ways. Some project into the connective tissue shealth of the c.n.s., which serves as a neurohaemal organ, either directly through the surface of a ganglion, or from the pleuro-cerebral or pleuro-parietal connectives. Other axons leave the c.n.s. via nerves leaving the left and right parietal and visceral ganglia; projections into the intestinal, anal, and internal right parietal nerves being most numerous. Axons which may be from either, or both Yellow Cells and Yellow-green Cells, can be found along the entire unbranched lengths of these nerves, and in subsequent branches which innervate organs lying in the anterior turn of the shell. All of these orgnas are closely associated with the lung cavity...

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Year:  1976        PMID: 8798     DOI: 10.1098/rstb.1976.0042

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  8 in total

1.  Functional morphology of the neuroendocrine sodium influx-stimulating peptide system of the pond snail, Lymnaea stagnalis, studied by in situ hybridization and immunocytochemistry.

Authors:  H H Boer; C Montagne-Wajer; J van Minnen; M Ramkema; P de Boer
Journal:  Cell Tissue Res       Date:  1992-06       Impact factor: 5.249

2.  Distribution of FMRFamide-like immunoreactivity in the nervous system of the slug Limax maximus.

Authors:  I R Cooke; A Gelperin
Journal:  Cell Tissue Res       Date:  1988-07       Impact factor: 5.249

3.  Functional morphology of the light yellow cell and yellow cell (sodium influx-stimulating peptide) neuroendocrine systems of the pond snail Lymnaea stagnalis.

Authors:  H H Boer; C Montagne-Wajer; F G Smith; D C Parish; M D Ramkema; R M Hoek; J van Minnen; P R Benjamin
Journal:  Cell Tissue Res       Date:  1994-02       Impact factor: 5.249

4.  An ultrastruct study of the innervation of the musculature of the pond snail Lymnaea stagnalis (L.) with reference to peripheral neurosecretion.

Authors:  B Plesch
Journal:  Cell Tissue Res       Date:  1977-09-30       Impact factor: 5.249

5.  Neurosecretion in the basommatophoran snail Bulinus truncatus (Gastropoda, Pulmonata).

Authors:  H H Boer; E W Roubos; H van Dalen; J R Groesbeek
Journal:  Cell Tissue Res       Date:  1977-01-05       Impact factor: 5.249

6.  Immunocytochemical demonstration of peptidergic cells in the pond snail Lymnaea stagnalis with an antiserum to the molluscan cardioactive tetrapeptide FMRF-amide.

Authors:  L P Schot; H H Boer
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

7.  An ultrastructural study of the neurosecretory canopy cell of the pond snail Lymnaea stagnalis (L.), with the use of the horseradish peroxidase tracer technique.

Authors:  J van Minnen; D Reichelt; J C Lodder
Journal:  Cell Tissue Res       Date:  1979       Impact factor: 5.249

8.  Gap Junction Coding Innexin in Lymnaea stagnalis: Sequence Analysis and Characterization in Tissues and the Central Nervous System.

Authors:  Brittany A Mersman; Sonia N Jolly; Zhenguo Lin; Fenglian Xu
Journal:  Front Synaptic Neurosci       Date:  2020-02-25
  8 in total

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