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Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion

Stick insects respond to visual or tactile stimuli with whole-body turning or directed reach-to-grasp movements. Such sensory-induced turning and reaching behaviour requires interneurons to convey information from sensory neuropils of the head ganglia to motor neuropils of the thoracic ganglia. To d...

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Autores principales: Goldammer, Jens, Büschges, Ansgar, Dürr, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470933/
https://www.ncbi.nlm.nih.gov/pubmed/37651417
http://dx.doi.org/10.1371/journal.pone.0290359
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author Goldammer, Jens
Büschges, Ansgar
Dürr, Volker
author_facet Goldammer, Jens
Büschges, Ansgar
Dürr, Volker
author_sort Goldammer, Jens
collection PubMed
description Stick insects respond to visual or tactile stimuli with whole-body turning or directed reach-to-grasp movements. Such sensory-induced turning and reaching behaviour requires interneurons to convey information from sensory neuropils of the head ganglia to motor neuropils of the thoracic ganglia. To date, descending interneurons are largely unknown in stick insects. In particular, it is unclear whether the special role of the front legs in sensory-induced turning and reaching has a neuroanatomical correlate in terms of descending interneuron numbers. Here, we describe the population of descending interneurons with somata in the brain or gnathal ganglion in the stick insect Carausius morosus, providing a first map of soma cluster counts and locations. By comparison of interneuron populations with projections to the pro- and mesothoracic ganglia, we then estimate the fraction of descending interneurons that terminate in the prothoracic ganglion. With regard to short-latency, touch-mediated reach-to-grasp movements, we also locate likely sites of synaptic interactions between antennal proprioceptive afferents to the deutocerebrum and gnathal ganglion with descending or ascending interneuron fibres. To this end, we combine fluorescent dye stainings of thoracic connectives with stainings of antennal hair field sensilla. Backfills of neck connectives revealed up to 410 descending interneuron somata (brain: 205 in 19 clusters; gnathal ganglion: 205). In comparison, backfills of the prothorax-mesothorax connectives stained only up to 173 somata (brain: 83 in 16 clusters; gnathal ganglion: 90), suggesting that up to 60% of all descending interneurons may terminate in the prothoracic ganglion (estimated upper bound). Double stainings of connectives and antennal hair field sensilla revealed that ascending or descending fibres arborise in close proximity of afferent terminals in the deutocerebrum and in the middle part of the gnathal ganglia. We conclude that two cephalothoracic pathways may convey cues about antennal movement and pointing direction to thoracic motor centres via two synapses only.
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spelling pubmed-104709332023-09-01 Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion Goldammer, Jens Büschges, Ansgar Dürr, Volker PLoS One Research Article Stick insects respond to visual or tactile stimuli with whole-body turning or directed reach-to-grasp movements. Such sensory-induced turning and reaching behaviour requires interneurons to convey information from sensory neuropils of the head ganglia to motor neuropils of the thoracic ganglia. To date, descending interneurons are largely unknown in stick insects. In particular, it is unclear whether the special role of the front legs in sensory-induced turning and reaching has a neuroanatomical correlate in terms of descending interneuron numbers. Here, we describe the population of descending interneurons with somata in the brain or gnathal ganglion in the stick insect Carausius morosus, providing a first map of soma cluster counts and locations. By comparison of interneuron populations with projections to the pro- and mesothoracic ganglia, we then estimate the fraction of descending interneurons that terminate in the prothoracic ganglion. With regard to short-latency, touch-mediated reach-to-grasp movements, we also locate likely sites of synaptic interactions between antennal proprioceptive afferents to the deutocerebrum and gnathal ganglion with descending or ascending interneuron fibres. To this end, we combine fluorescent dye stainings of thoracic connectives with stainings of antennal hair field sensilla. Backfills of neck connectives revealed up to 410 descending interneuron somata (brain: 205 in 19 clusters; gnathal ganglion: 205). In comparison, backfills of the prothorax-mesothorax connectives stained only up to 173 somata (brain: 83 in 16 clusters; gnathal ganglion: 90), suggesting that up to 60% of all descending interneurons may terminate in the prothoracic ganglion (estimated upper bound). Double stainings of connectives and antennal hair field sensilla revealed that ascending or descending fibres arborise in close proximity of afferent terminals in the deutocerebrum and in the middle part of the gnathal ganglia. We conclude that two cephalothoracic pathways may convey cues about antennal movement and pointing direction to thoracic motor centres via two synapses only. Public Library of Science 2023-08-31 /pmc/articles/PMC10470933/ /pubmed/37651417 http://dx.doi.org/10.1371/journal.pone.0290359 Text en © 2023 Goldammer et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Goldammer, Jens
Büschges, Ansgar
Dürr, Volker
Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title_full Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title_fullStr Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title_full_unstemmed Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title_short Descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
title_sort descending interneurons of the stick insect connecting brain neuropiles with the prothoracic ganglion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470933/
https://www.ncbi.nlm.nih.gov/pubmed/37651417
http://dx.doi.org/10.1371/journal.pone.0290359
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