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Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments

Due to the relatively small number of neurons (few tens of thousands), the well-established multipurpose model organism Lymnaea stagnalis, great pond snail, has been extensively used to study the functioning of the nervous system. Unlike the more complex brains of higher organisms, L. stagnalis has...

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Autores principales: Wood, Ellen A., Stopka, Sylwia A., Zhang, Linwen, Mattson, Sara, Maasz, Gabor, Pirger, Zsolt, Vertes, Akos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172996/
https://www.ncbi.nlm.nih.gov/pubmed/34093125
http://dx.doi.org/10.3389/fnmol.2021.670303
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author Wood, Ellen A.
Stopka, Sylwia A.
Zhang, Linwen
Mattson, Sara
Maasz, Gabor
Pirger, Zsolt
Vertes, Akos
author_facet Wood, Ellen A.
Stopka, Sylwia A.
Zhang, Linwen
Mattson, Sara
Maasz, Gabor
Pirger, Zsolt
Vertes, Akos
author_sort Wood, Ellen A.
collection PubMed
description Due to the relatively small number of neurons (few tens of thousands), the well-established multipurpose model organism Lymnaea stagnalis, great pond snail, has been extensively used to study the functioning of the nervous system. Unlike the more complex brains of higher organisms, L. stagnalis has a relatively simple central nervous system (CNS) with well-defined circuits (e.g., feeding, locomotion, learning, and memory) and identified individual neurons (e.g., cerebral giant cell, CGC), which generate behavioral patterns. Accumulating information from electrophysiological experiments maps the network of neuronal connections and the neuronal circuits responsible for basic life functions. Chemical signaling between synaptic-coupled neurons is underpinned by neurotransmitters and neuropeptides. This review looks at the rapidly expanding contributions of mass spectrometry (MS) to neuropeptide discovery and identification at different granularity of CNS organization. Abundances and distributions of neuropeptides in the whole CNS, eleven interconnected ganglia, neuronal clusters, single neurons, and subcellular compartments are captured by MS imaging and single cell analysis techniques. Combining neuropeptide expression and electrophysiological data, and aided by genomic and transcriptomic information, the molecular basis of CNS-controlled biological functions is increasingly revealed.
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spelling pubmed-81729962021-06-04 Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments Wood, Ellen A. Stopka, Sylwia A. Zhang, Linwen Mattson, Sara Maasz, Gabor Pirger, Zsolt Vertes, Akos Front Mol Neurosci Neuroscience Due to the relatively small number of neurons (few tens of thousands), the well-established multipurpose model organism Lymnaea stagnalis, great pond snail, has been extensively used to study the functioning of the nervous system. Unlike the more complex brains of higher organisms, L. stagnalis has a relatively simple central nervous system (CNS) with well-defined circuits (e.g., feeding, locomotion, learning, and memory) and identified individual neurons (e.g., cerebral giant cell, CGC), which generate behavioral patterns. Accumulating information from electrophysiological experiments maps the network of neuronal connections and the neuronal circuits responsible for basic life functions. Chemical signaling between synaptic-coupled neurons is underpinned by neurotransmitters and neuropeptides. This review looks at the rapidly expanding contributions of mass spectrometry (MS) to neuropeptide discovery and identification at different granularity of CNS organization. Abundances and distributions of neuropeptides in the whole CNS, eleven interconnected ganglia, neuronal clusters, single neurons, and subcellular compartments are captured by MS imaging and single cell analysis techniques. Combining neuropeptide expression and electrophysiological data, and aided by genomic and transcriptomic information, the molecular basis of CNS-controlled biological functions is increasingly revealed. Frontiers Media S.A. 2021-05-20 /pmc/articles/PMC8172996/ /pubmed/34093125 http://dx.doi.org/10.3389/fnmol.2021.670303 Text en Copyright © 2021 Wood, Stopka, Zhang, Mattson, Maasz, Pirger and Vertes. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wood, Ellen A.
Stopka, Sylwia A.
Zhang, Linwen
Mattson, Sara
Maasz, Gabor
Pirger, Zsolt
Vertes, Akos
Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title_full Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title_fullStr Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title_full_unstemmed Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title_short Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments
title_sort neuropeptide localization in lymnaea stagnalis: from the central nervous system to subcellular compartments
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172996/
https://www.ncbi.nlm.nih.gov/pubmed/34093125
http://dx.doi.org/10.3389/fnmol.2021.670303
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