Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rue, Mara C. P., Baas‐Thomas, Natasha, Iyengar, Priya S., Scaria, Lara K., Marder, Eve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784807864741658624
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
title_full Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
title_fullStr Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
title_full_unstemmed Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
title_short Localization of chemical synapses and modulatory release sites in the cardiac ganglion of the crab, Cancer borealis
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
work_keys_str_mv AT ruemaracp localizationofchemicalsynapsesandmodulatoryreleasesitesinthecardiacganglionofthecrabcancerborealis
AT baasthomasnatasha localizationofchemicalsynapsesandmodulatoryreleasesitesinthecardiacganglionofthecrabcancerborealis
AT iyengarpriyas localizationofchemicalsynapsesandmodulatoryreleasesitesinthecardiacganglionofthecrabcancerborealis
AT scarialarak localizationofchemicalsynapsesandmodulatoryreleasesitesinthecardiacganglionofthecrabcancerborealis
AT mardereve localizationofchemicalsynapsesandmodulatoryreleasesitesinthecardiacganglionofthecrabcancerborealis