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Circadian Rhythms of Perineuronal Net Composition

Perineuronal nets (PNNs) are extracellular matrix (ECM) structures that envelop neurons and regulate synaptic functions. Long thought to be stable structures, PNNs have been recently shown to respond dynamically during learning, potentially regulating the formation of new synapses. We postulated tha...

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Autores principales: Pantazopoulos, Harry, Gisabella, Barbara, Rexrode, Lindsay, Benefield, David, Yildiz, Emrah, Seltzer, Phoebe, Valeri, Jake, Chelini, Gabriele, Reich, Anna, Ardelt, Magdalena, Berretta, Sabina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405073/
https://www.ncbi.nlm.nih.gov/pubmed/32719104
http://dx.doi.org/10.1523/ENEURO.0034-19.2020
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author Pantazopoulos, Harry
Gisabella, Barbara
Rexrode, Lindsay
Benefield, David
Yildiz, Emrah
Seltzer, Phoebe
Valeri, Jake
Chelini, Gabriele
Reich, Anna
Ardelt, Magdalena
Berretta, Sabina
author_facet Pantazopoulos, Harry
Gisabella, Barbara
Rexrode, Lindsay
Benefield, David
Yildiz, Emrah
Seltzer, Phoebe
Valeri, Jake
Chelini, Gabriele
Reich, Anna
Ardelt, Magdalena
Berretta, Sabina
author_sort Pantazopoulos, Harry
collection PubMed
description Perineuronal nets (PNNs) are extracellular matrix (ECM) structures that envelop neurons and regulate synaptic functions. Long thought to be stable structures, PNNs have been recently shown to respond dynamically during learning, potentially regulating the formation of new synapses. We postulated that PNNs vary during sleep, a period of active synaptic modification. Notably, PNN components are cleaved by matrix proteases such as the protease cathepsin-S. This protease is diurnally expressed in the mouse cortex, coinciding with dendritic spine density rhythms. Thus, cathepsin-S may contribute to PNN remodeling during sleep, mediating synaptic reorganization. These studies were designed to test the hypothesis that PNN numbers vary in a diurnal manner in the rodent and human brain, as well as in a circadian manner in the rodent brain, and that these rhythms are disrupted by sleep deprivation. In mice, we observed diurnal and circadian rhythms of PNNs labeled with the lectin Wisteria floribunda agglutinin (WFA+ PNNs) in several brain regions involved in emotional memory processing. Sleep deprivation prevented the daytime decrease of WFA+ PNNs and enhances fear memory extinction. Diurnal rhythms of cathepsin-S expression in microglia were observed in the same brain regions, opposite to PNN rhythms. Finally, incubation of mouse sections with cathepsin-S eliminated PNN labeling. In humans, WFA+ PNNs showed a diurnal rhythm in the amygdala and thalamic reticular nucleus (TRN). Our results demonstrate that PNNs vary in a circadian manner and this is disrupted by sleep deprivation. We suggest that rhythmic modification of PNNs may contribute to memory consolidation during sleep.
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spelling pubmed-74050732020-08-05 Circadian Rhythms of Perineuronal Net Composition Pantazopoulos, Harry Gisabella, Barbara Rexrode, Lindsay Benefield, David Yildiz, Emrah Seltzer, Phoebe Valeri, Jake Chelini, Gabriele Reich, Anna Ardelt, Magdalena Berretta, Sabina eNeuro Research Article: New Research Perineuronal nets (PNNs) are extracellular matrix (ECM) structures that envelop neurons and regulate synaptic functions. Long thought to be stable structures, PNNs have been recently shown to respond dynamically during learning, potentially regulating the formation of new synapses. We postulated that PNNs vary during sleep, a period of active synaptic modification. Notably, PNN components are cleaved by matrix proteases such as the protease cathepsin-S. This protease is diurnally expressed in the mouse cortex, coinciding with dendritic spine density rhythms. Thus, cathepsin-S may contribute to PNN remodeling during sleep, mediating synaptic reorganization. These studies were designed to test the hypothesis that PNN numbers vary in a diurnal manner in the rodent and human brain, as well as in a circadian manner in the rodent brain, and that these rhythms are disrupted by sleep deprivation. In mice, we observed diurnal and circadian rhythms of PNNs labeled with the lectin Wisteria floribunda agglutinin (WFA+ PNNs) in several brain regions involved in emotional memory processing. Sleep deprivation prevented the daytime decrease of WFA+ PNNs and enhances fear memory extinction. Diurnal rhythms of cathepsin-S expression in microglia were observed in the same brain regions, opposite to PNN rhythms. Finally, incubation of mouse sections with cathepsin-S eliminated PNN labeling. In humans, WFA+ PNNs showed a diurnal rhythm in the amygdala and thalamic reticular nucleus (TRN). Our results demonstrate that PNNs vary in a circadian manner and this is disrupted by sleep deprivation. We suggest that rhythmic modification of PNNs may contribute to memory consolidation during sleep. Society for Neuroscience 2020-07-31 /pmc/articles/PMC7405073/ /pubmed/32719104 http://dx.doi.org/10.1523/ENEURO.0034-19.2020 Text en Copyright © 2020 Pantazopoulos et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Pantazopoulos, Harry
Gisabella, Barbara
Rexrode, Lindsay
Benefield, David
Yildiz, Emrah
Seltzer, Phoebe
Valeri, Jake
Chelini, Gabriele
Reich, Anna
Ardelt, Magdalena
Berretta, Sabina
Circadian Rhythms of Perineuronal Net Composition
title Circadian Rhythms of Perineuronal Net Composition
title_full Circadian Rhythms of Perineuronal Net Composition
title_fullStr Circadian Rhythms of Perineuronal Net Composition
title_full_unstemmed Circadian Rhythms of Perineuronal Net Composition
title_short Circadian Rhythms of Perineuronal Net Composition
title_sort circadian rhythms of perineuronal net composition
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7405073/
https://www.ncbi.nlm.nih.gov/pubmed/32719104
http://dx.doi.org/10.1523/ENEURO.0034-19.2020
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