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Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
The crustacean cardiac ganglion (CG) comprises nine neurons that provide rhythmic drive to the heart. The CG is the direct target of multiple modulators. Synapsin‐like immunoreactivity was found clustered around the somata of the large cells (LC) and in a neuropil at the anterior branch of the CG tr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560961/ https://www.ncbi.nlm.nih.gov/pubmed/35882035 http://dx.doi.org/10.1002/cne.25385 |
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author | Rue, Mara C. P. Baas‐Thomas, Natasha Iyengar, Priya S. Scaria, Lara K. Marder, Eve |
author_facet | Rue, Mara C. P. Baas‐Thomas, Natasha Iyengar, Priya S. Scaria, Lara K. Marder, Eve |
author_sort | Rue, Mara C. P. |
collection | PubMed |
description | The crustacean cardiac ganglion (CG) comprises nine neurons that provide rhythmic drive to the heart. The CG is the direct target of multiple modulators. Synapsin‐like immunoreactivity was found clustered around the somata of the large cells (LC) and in a neuropil at the anterior branch of the CG trunk of Cancer borealis. This implicates the soma as a key site of synaptic integration, an unusual configuration in invertebrates. Proctolin is an excitatory neuromodulator of the CG, and proctolin‐like immunoreactivity exhibited partial overlap with putative chemical synapses near the LCs and at the neuropil. A proctolin‐like projection was also found in a pair of excitatory nerves entering the CG. GABA‐like immunoreactivity was nearly completely colocalized with chemical synapses near the LCs but absent at the anterior branch neuropil. GABA‐like projections were found in a pair of inhibitory nerves entering the CG. C. borealis Allatostatin B1 (CbASTB), red pigment concentrating hormone, and FLRFamide‐like immunoreactivity each had a unique pattern of staining and co‐localization with putative chemical synapses. These results provide morphological evidence that synaptic input is integrated at LC somata in the CG. Our findings provide a topographical organization for some of the multiple inhibitory and excitatory modulators that alter the rhythmic output of this semi‐autonomous motor circuit. |
format | Online Article Text |
id | pubmed-9560961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95609612022-12-01 Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis Rue, Mara C. P. Baas‐Thomas, Natasha Iyengar, Priya S. Scaria, Lara K. Marder, Eve J Comp Neurol Research Articles The crustacean cardiac ganglion (CG) comprises nine neurons that provide rhythmic drive to the heart. The CG is the direct target of multiple modulators. Synapsin‐like immunoreactivity was found clustered around the somata of the large cells (LC) and in a neuropil at the anterior branch of the CG trunk of Cancer borealis. This implicates the soma as a key site of synaptic integration, an unusual configuration in invertebrates. Proctolin is an excitatory neuromodulator of the CG, and proctolin‐like immunoreactivity exhibited partial overlap with putative chemical synapses near the LCs and at the neuropil. A proctolin‐like projection was also found in a pair of excitatory nerves entering the CG. GABA‐like immunoreactivity was nearly completely colocalized with chemical synapses near the LCs but absent at the anterior branch neuropil. GABA‐like projections were found in a pair of inhibitory nerves entering the CG. C. borealis Allatostatin B1 (CbASTB), red pigment concentrating hormone, and FLRFamide‐like immunoreactivity each had a unique pattern of staining and co‐localization with putative chemical synapses. These results provide morphological evidence that synaptic input is integrated at LC somata in the CG. Our findings provide a topographical organization for some of the multiple inhibitory and excitatory modulators that alter the rhythmic output of this semi‐autonomous motor circuit. John Wiley and Sons Inc. 2022-07-26 2022-12 /pmc/articles/PMC9560961/ /pubmed/35882035 http://dx.doi.org/10.1002/cne.25385 Text en © 2022 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Rue, Mara C. P. Baas‐Thomas, Natasha Iyengar, Priya S. Scaria, Lara K. Marder, Eve Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis |
title | Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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title_full | Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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title_fullStr | Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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title_full_unstemmed | Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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title_short | Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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title_sort | localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, cancer borealis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560961/ https://www.ncbi.nlm.nih.gov/pubmed/35882035 http://dx.doi.org/10.1002/cne.25385 |
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