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Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus

The mammalian pacemaker in the suprachiasmatic nucleus (SCN) contains a population of neural oscillators capable of sustaining cell-autonomous rhythms in gene expression and electrical firing. A critical question for understanding pacemaker function is how SCN oscillators are organized into a cohere...

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Detalles Bibliográficos
Autores principales: Evans, Jennifer A., Leise, Tanya L., Castanon-Cervantes, Oscar, Davidson, Alec J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017566/
https://www.ncbi.nlm.nih.gov/pubmed/21249213
http://dx.doi.org/10.1371/journal.pone.0015869
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author Evans, Jennifer A.
Leise, Tanya L.
Castanon-Cervantes, Oscar
Davidson, Alec J.
author_facet Evans, Jennifer A.
Leise, Tanya L.
Castanon-Cervantes, Oscar
Davidson, Alec J.
author_sort Evans, Jennifer A.
collection PubMed
description The mammalian pacemaker in the suprachiasmatic nucleus (SCN) contains a population of neural oscillators capable of sustaining cell-autonomous rhythms in gene expression and electrical firing. A critical question for understanding pacemaker function is how SCN oscillators are organized into a coherent tissue capable of coordinating circadian rhythms in behavior and physiology. Here we undertake a comprehensive analysis of oscillatory function across the SCN of the adult PER2::LUC mouse by developing a novel approach involving multi-position bioluminescence imaging and unbiased computational analyses. We demonstrate that there is phase heterogeneity across all three dimensions of the SCN that is intrinsically regulated and extrinsically modulated by light in a region-specific manner. By investigating the mechanistic bases of SCN phase heterogeneity, we show for the first time that phase differences are not systematically related to regional differences in period, waveform, amplitude, or brightness. Furthermore, phase differences are not related to regional differences in the expression of arginine vasopressin and vasoactive intestinal polypeptide, two key neuropeptides characterizing functionally distinct subdivisions of the SCN. The consistency of SCN spatiotemporal organization across individuals and across planes of section suggests that the precise phasing of oscillators is a robust feature of the pacemaker important for its function.
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spelling pubmed-30175662011-01-19 Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus Evans, Jennifer A. Leise, Tanya L. Castanon-Cervantes, Oscar Davidson, Alec J. PLoS One Research Article The mammalian pacemaker in the suprachiasmatic nucleus (SCN) contains a population of neural oscillators capable of sustaining cell-autonomous rhythms in gene expression and electrical firing. A critical question for understanding pacemaker function is how SCN oscillators are organized into a coherent tissue capable of coordinating circadian rhythms in behavior and physiology. Here we undertake a comprehensive analysis of oscillatory function across the SCN of the adult PER2::LUC mouse by developing a novel approach involving multi-position bioluminescence imaging and unbiased computational analyses. We demonstrate that there is phase heterogeneity across all three dimensions of the SCN that is intrinsically regulated and extrinsically modulated by light in a region-specific manner. By investigating the mechanistic bases of SCN phase heterogeneity, we show for the first time that phase differences are not systematically related to regional differences in period, waveform, amplitude, or brightness. Furthermore, phase differences are not related to regional differences in the expression of arginine vasopressin and vasoactive intestinal polypeptide, two key neuropeptides characterizing functionally distinct subdivisions of the SCN. The consistency of SCN spatiotemporal organization across individuals and across planes of section suggests that the precise phasing of oscillators is a robust feature of the pacemaker important for its function. Public Library of Science 2011-01-07 /pmc/articles/PMC3017566/ /pubmed/21249213 http://dx.doi.org/10.1371/journal.pone.0015869 Text en Evans et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Evans, Jennifer A.
Leise, Tanya L.
Castanon-Cervantes, Oscar
Davidson, Alec J.
Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title_full Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title_fullStr Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title_full_unstemmed Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title_short Intrinsic Regulation of Spatiotemporal Organization within the Suprachiasmatic Nucleus
title_sort intrinsic regulation of spatiotemporal organization within the suprachiasmatic nucleus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017566/
https://www.ncbi.nlm.nih.gov/pubmed/21249213
http://dx.doi.org/10.1371/journal.pone.0015869
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