Cargando…

The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S

Microglia are thought to play important roles in the maintenance of neuronal circuitry and the regulation of behavior. We found that the cortical microglia contain an intrinsic molecular clock and exhibit a circadian expression of cathepsin S (CatS), a microglia-specific lysosomal cysteine protease...

Descripción completa

Detalles Bibliográficos
Autores principales: Hayashi, Yoshinori, Koyanagi, Satoru, Kusunose, Naoki, Okada, Ryo, Wu, Zhou, Tozaki-Saitoh, Hidetoshi, Ukai, Kiyoharu, Kohsaka, Shinichi, Inoue, Kazuhide, Ohdo, Shigehiro, Nakanishi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783043/
https://www.ncbi.nlm.nih.gov/pubmed/24067868
http://dx.doi.org/10.1038/srep02744
_version_ 1782285627124875264
author Hayashi, Yoshinori
Koyanagi, Satoru
Kusunose, Naoki
Okada, Ryo
Wu, Zhou
Tozaki-Saitoh, Hidetoshi
Ukai, Kiyoharu
Kohsaka, Shinichi
Inoue, Kazuhide
Ohdo, Shigehiro
Nakanishi, Hiroshi
author_facet Hayashi, Yoshinori
Koyanagi, Satoru
Kusunose, Naoki
Okada, Ryo
Wu, Zhou
Tozaki-Saitoh, Hidetoshi
Ukai, Kiyoharu
Kohsaka, Shinichi
Inoue, Kazuhide
Ohdo, Shigehiro
Nakanishi, Hiroshi
author_sort Hayashi, Yoshinori
collection PubMed
description Microglia are thought to play important roles in the maintenance of neuronal circuitry and the regulation of behavior. We found that the cortical microglia contain an intrinsic molecular clock and exhibit a circadian expression of cathepsin S (CatS), a microglia-specific lysosomal cysteine protease in the brain. The genetic deletion of CatS causes mice to exhibit hyperlocomotor activity and removes diurnal variations in the synaptic activity and spine density of the cortical neurons, which are significantly higher during the dark (waking) phase than the light (sleeping) phase. Furthermore, incubation with recombinant CatS significantly reduced the synaptic activity of the cortical neurons. These results suggest that CatS secreted by microglia during the dark-phase decreases the spine density of the cortical neurons by modifying the perisynaptic environment, leading to downscaling of the synaptic strength during the subsequent light-phase. Disruption of CatS therefore induces hyperlocomotor activity due to failure to downscale the synaptic strength.
format Online
Article
Text
id pubmed-3783043
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-37830432013-09-25 The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S Hayashi, Yoshinori Koyanagi, Satoru Kusunose, Naoki Okada, Ryo Wu, Zhou Tozaki-Saitoh, Hidetoshi Ukai, Kiyoharu Kohsaka, Shinichi Inoue, Kazuhide Ohdo, Shigehiro Nakanishi, Hiroshi Sci Rep Article Microglia are thought to play important roles in the maintenance of neuronal circuitry and the regulation of behavior. We found that the cortical microglia contain an intrinsic molecular clock and exhibit a circadian expression of cathepsin S (CatS), a microglia-specific lysosomal cysteine protease in the brain. The genetic deletion of CatS causes mice to exhibit hyperlocomotor activity and removes diurnal variations in the synaptic activity and spine density of the cortical neurons, which are significantly higher during the dark (waking) phase than the light (sleeping) phase. Furthermore, incubation with recombinant CatS significantly reduced the synaptic activity of the cortical neurons. These results suggest that CatS secreted by microglia during the dark-phase decreases the spine density of the cortical neurons by modifying the perisynaptic environment, leading to downscaling of the synaptic strength during the subsequent light-phase. Disruption of CatS therefore induces hyperlocomotor activity due to failure to downscale the synaptic strength. Nature Publishing Group 2013-09-25 /pmc/articles/PMC3783043/ /pubmed/24067868 http://dx.doi.org/10.1038/srep02744 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Hayashi, Yoshinori
Koyanagi, Satoru
Kusunose, Naoki
Okada, Ryo
Wu, Zhou
Tozaki-Saitoh, Hidetoshi
Ukai, Kiyoharu
Kohsaka, Shinichi
Inoue, Kazuhide
Ohdo, Shigehiro
Nakanishi, Hiroshi
The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title_full The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title_fullStr The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title_full_unstemmed The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title_short The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S
title_sort intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin s
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783043/
https://www.ncbi.nlm.nih.gov/pubmed/24067868
http://dx.doi.org/10.1038/srep02744
work_keys_str_mv AT hayashiyoshinori theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT koyanagisatoru theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT kusunosenaoki theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT okadaryo theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT wuzhou theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT tozakisaitohhidetoshi theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT ukaikiyoharu theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT kohsakashinichi theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT inouekazuhide theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT ohdoshigehiro theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT nakanishihiroshi theintrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT hayashiyoshinori intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT koyanagisatoru intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT kusunosenaoki intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT okadaryo intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT wuzhou intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT tozakisaitohhidetoshi intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT ukaikiyoharu intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT kohsakashinichi intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT inouekazuhide intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT ohdoshigehiro intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins
AT nakanishihiroshi intrinsicmicroglialmolecularclockcontrolssynapticstrengthviathecircadianexpressionofcathepsins