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Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae
Lesion and transplantation studies in the cockroach, Leucophaea maderae, have located its bilaterally symmetric circadian pacemakers necessary for driving circadian locomotor activity rhythms to the accessory medulla of the optic lobes. The accessory medulla comprises a network of peptidergic neuron...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046342/ https://www.ncbi.nlm.nih.gov/pubmed/21229364 http://dx.doi.org/10.1007/s00441-010-1091-4 |
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author | Soehler, Sandra Stengl, Monika Reischig, Thomas |
author_facet | Soehler, Sandra Stengl, Monika Reischig, Thomas |
author_sort | Soehler, Sandra |
collection | PubMed |
description | Lesion and transplantation studies in the cockroach, Leucophaea maderae, have located its bilaterally symmetric circadian pacemakers necessary for driving circadian locomotor activity rhythms to the accessory medulla of the optic lobes. The accessory medulla comprises a network of peptidergic neurons, including pigment-dispersing factor (PDF)-expressing presumptive circadian pacemaker cells. At least three of the PDF-expressing neurons directly connect the two accessory medullae, apparently as a circadian coupling pathway. Here, the PDF-expressing circadian coupling pathways were examined for peptide colocalization by tracer experiments and double-label immunohistochemistry with antisera against PDF, FMRFamide, and Asn(13)-orcokinin. A fourth group of contralaterally projecting medulla neurons was identified, additional to the three known groups. Group one of the contralaterally projecting medulla neurons contained up to four PDF-expressing cells. Of these, three medium-sized PDF-immunoreactive neurons coexpressed FMRFamide and Asn(13)-orcokinin immunoreactivity. However, the contralaterally projecting largest PDF neuron showed no further peptide colocalization, as was also the case for the other large PDF-expressing medulla cells, allowing the easy identification of this cell group. Although two-thirds of all PDF-expressing medulla neurons coexpressed FMRFamide and orcokinin immunoreactivity in their somata, colocalization of PDF and FMRFamide immunoreactivity was observed in only a few termination sites. Colocalization of PDF and orcokinin immunoreactivity was never observed in any of the terminals or optic commissures. We suggest that circadian pacemaker cells employ axonal peptide sorting to phase-control physiological processes at specific times of the day. |
format | Text |
id | pubmed-3046342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30463422011-04-05 Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae Soehler, Sandra Stengl, Monika Reischig, Thomas Cell Tissue Res Regular Article Lesion and transplantation studies in the cockroach, Leucophaea maderae, have located its bilaterally symmetric circadian pacemakers necessary for driving circadian locomotor activity rhythms to the accessory medulla of the optic lobes. The accessory medulla comprises a network of peptidergic neurons, including pigment-dispersing factor (PDF)-expressing presumptive circadian pacemaker cells. At least three of the PDF-expressing neurons directly connect the two accessory medullae, apparently as a circadian coupling pathway. Here, the PDF-expressing circadian coupling pathways were examined for peptide colocalization by tracer experiments and double-label immunohistochemistry with antisera against PDF, FMRFamide, and Asn(13)-orcokinin. A fourth group of contralaterally projecting medulla neurons was identified, additional to the three known groups. Group one of the contralaterally projecting medulla neurons contained up to four PDF-expressing cells. Of these, three medium-sized PDF-immunoreactive neurons coexpressed FMRFamide and Asn(13)-orcokinin immunoreactivity. However, the contralaterally projecting largest PDF neuron showed no further peptide colocalization, as was also the case for the other large PDF-expressing medulla cells, allowing the easy identification of this cell group. Although two-thirds of all PDF-expressing medulla neurons coexpressed FMRFamide and orcokinin immunoreactivity in their somata, colocalization of PDF and FMRFamide immunoreactivity was observed in only a few termination sites. Colocalization of PDF and orcokinin immunoreactivity was never observed in any of the terminals or optic commissures. We suggest that circadian pacemaker cells employ axonal peptide sorting to phase-control physiological processes at specific times of the day. Springer-Verlag 2011-01-14 2011 /pmc/articles/PMC3046342/ /pubmed/21229364 http://dx.doi.org/10.1007/s00441-010-1091-4 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Regular Article Soehler, Sandra Stengl, Monika Reischig, Thomas Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title | Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title_full | Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title_fullStr | Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title_full_unstemmed | Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title_short | Circadian pacemaker coupling by multi-peptidergic neurons in the cockroach Leucophaea maderae |
title_sort | circadian pacemaker coupling by multi-peptidergic neurons in the cockroach leucophaea maderae |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046342/ https://www.ncbi.nlm.nih.gov/pubmed/21229364 http://dx.doi.org/10.1007/s00441-010-1091-4 |
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