Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in mice
Copyright © 2024 The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University. Published by Elsevier Inc. All rights reserved..
Epilepsy is a brain disorder affecting up to 1 in 26 individuals. Despite its clinical importance, the molecular mechanisms of epileptogenesis are still far from clarified. Our previous study showed that disruption of Clock in excitatory neurons alters cortical circuits and leads to generation of focal epilepsy. In this study, a GAD-Cre;Clockflox/flox mouse line with conditional Clock gene knockout in inhibitory neurons was established. We observed that seizure latency was prolonged, the severity and mortality of pilocarpine-induced seizure were significantly reduced, and memory was improved in GAD-Cre;Clockflox/flox mice. We hypothesize that mice with CLOCK knockout in inhibitory neurons have increased threshold for seizure, opposite from mice with CLOCK knockout in excitatory neurons. Further investigation showed Clock knockout in inhibitory neurons upregulated the basal protein level of ARC, a synaptic plasticity-associated immediate-early gene product, likely through the BDNF-ERK pathway. Altered basal levels of ARC may play an important role in epileptogenesis after Clock deletion in inhibitory neurons. Although sEPSCs and intrinsic properties of layer 5 pyramidal neurons in the somatosensory cortex exhibit no changes, the spine density increased in apical dendrite of pyramidal neurons in CLOCK knockout group. Our results suggest an underlying mechanism by which the circadian protein CLOCK in inhibitory neurons participates in neuronal activity and regulates the predisposition to epilepsy.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:193 |
---|---|
Enthalten in: |
Neurobiology of disease - 193(2024) vom: 29. März, Seite 106457 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Deng, Lu [VerfasserIn] |
---|
Links: |
---|
Themen: |
ARC |
---|
Anmerkungen: |
Date Completed 26.03.2024 Date Revised 28.03.2024 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.nbd.2024.106457 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM36913091X |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM36913091X | ||
003 | DE-627 | ||
005 | 20240329000631.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240301s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.nbd.2024.106457 |2 doi | |
028 | 5 | 2 | |a pubmed24n1353.xml |
035 | |a (DE-627)NLM36913091X | ||
035 | |a (NLM)38423191 | ||
035 | |a (PII)S0969-9961(24)00056-1 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Deng, Lu |e verfasserin |4 aut | |
245 | 1 | 0 | |a Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in mice |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 26.03.2024 | ||
500 | |a Date Revised 28.03.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2024 The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University. Published by Elsevier Inc. All rights reserved. | ||
520 | |a Epilepsy is a brain disorder affecting up to 1 in 26 individuals. Despite its clinical importance, the molecular mechanisms of epileptogenesis are still far from clarified. Our previous study showed that disruption of Clock in excitatory neurons alters cortical circuits and leads to generation of focal epilepsy. In this study, a GAD-Cre;Clockflox/flox mouse line with conditional Clock gene knockout in inhibitory neurons was established. We observed that seizure latency was prolonged, the severity and mortality of pilocarpine-induced seizure were significantly reduced, and memory was improved in GAD-Cre;Clockflox/flox mice. We hypothesize that mice with CLOCK knockout in inhibitory neurons have increased threshold for seizure, opposite from mice with CLOCK knockout in excitatory neurons. Further investigation showed Clock knockout in inhibitory neurons upregulated the basal protein level of ARC, a synaptic plasticity-associated immediate-early gene product, likely through the BDNF-ERK pathway. Altered basal levels of ARC may play an important role in epileptogenesis after Clock deletion in inhibitory neurons. Although sEPSCs and intrinsic properties of layer 5 pyramidal neurons in the somatosensory cortex exhibit no changes, the spine density increased in apical dendrite of pyramidal neurons in CLOCK knockout group. Our results suggest an underlying mechanism by which the circadian protein CLOCK in inhibitory neurons participates in neuronal activity and regulates the predisposition to epilepsy | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a ARC | |
650 | 4 | |a CLOCK | |
650 | 4 | |a Epilepsy | |
650 | 4 | |a Inhibitory neurons | |
650 | 7 | |a Clock protein, mouse |2 NLM | |
650 | 7 | |a EC 2.3.1.48 |2 NLM | |
700 | 1 | |a Jiang, Hong |e verfasserin |4 aut | |
700 | 1 | |a Lin, Jingjing |e verfasserin |4 aut | |
700 | 1 | |a Xu, Di |e verfasserin |4 aut | |
700 | 1 | |a Qi, Ailin |e verfasserin |4 aut | |
700 | 1 | |a Guo, Qing |e verfasserin |4 aut | |
700 | 1 | |a Li, Ping-Ping |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xinshi |e verfasserin |4 aut | |
700 | 1 | |a Liu, Judy S |e verfasserin |4 aut | |
700 | 1 | |a Fu, Xiaoqin |e verfasserin |4 aut | |
700 | 1 | |a Li, Peijun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Neurobiology of disease |d 1997 |g 193(2024) vom: 29. März, Seite 106457 |w (DE-627)NLM089461223 |x 1095-953X |7 nnns |
773 | 1 | 8 | |g volume:193 |g year:2024 |g day:29 |g month:03 |g pages:106457 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.nbd.2024.106457 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 193 |j 2024 |b 29 |c 03 |h 106457 |