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p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus
PAK1 inhibitors are known to markedly improve social and cognitive function in several animal models of brain disorders, including autism, but the underlying mechanisms remain elusive. We show here that disruption of PAK1 in mice suppresses inhibitory neurotransmission through an increase in tonic,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907698/ https://www.ncbi.nlm.nih.gov/pubmed/27296803 http://dx.doi.org/10.7554/eLife.14653 |
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author | Xia, Shuting Zhou, Zikai Leung, Celeste Zhu, Yuehua Pan, Xingxiu Qi, Junxia Morena, Maria Hill, Matthew N Xie, Wei Jia, Zhengping |
author_facet | Xia, Shuting Zhou, Zikai Leung, Celeste Zhu, Yuehua Pan, Xingxiu Qi, Junxia Morena, Maria Hill, Matthew N Xie, Wei Jia, Zhengping |
author_sort | Xia, Shuting |
collection | PubMed |
description | PAK1 inhibitors are known to markedly improve social and cognitive function in several animal models of brain disorders, including autism, but the underlying mechanisms remain elusive. We show here that disruption of PAK1 in mice suppresses inhibitory neurotransmission through an increase in tonic, but not phasic, secretion of endocannabinoids (eCB). Consistently, we found elevated levels of anandamide (AEA), but not 2-arachidonoylglycerol (2-AG) following PAK1 disruption. This increased tonic AEA signaling is mediated by reduced cyclooxygenase-2 (COX-2), and COX-2 inhibitors recapitulate the effect of PAK1 deletion on GABAergic transmission in a CB1 receptor-dependent manner. These results establish a novel signaling process whereby PAK1 upregulates COX-2, reduces AEA and restricts tonic eCB-mediated processes. Because PAK1 and eCB are both critically involved in many other organ systems in addition to the brain, our findings may provide a unified mechanism by which PAK1 regulates these systems and their dysfunctions including cancers, inflammations and allergies. DOI: http://dx.doi.org/10.7554/eLife.14653.001 |
format | Online Article Text |
id | pubmed-4907698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49076982016-06-16 p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus Xia, Shuting Zhou, Zikai Leung, Celeste Zhu, Yuehua Pan, Xingxiu Qi, Junxia Morena, Maria Hill, Matthew N Xie, Wei Jia, Zhengping eLife Neuroscience PAK1 inhibitors are known to markedly improve social and cognitive function in several animal models of brain disorders, including autism, but the underlying mechanisms remain elusive. We show here that disruption of PAK1 in mice suppresses inhibitory neurotransmission through an increase in tonic, but not phasic, secretion of endocannabinoids (eCB). Consistently, we found elevated levels of anandamide (AEA), but not 2-arachidonoylglycerol (2-AG) following PAK1 disruption. This increased tonic AEA signaling is mediated by reduced cyclooxygenase-2 (COX-2), and COX-2 inhibitors recapitulate the effect of PAK1 deletion on GABAergic transmission in a CB1 receptor-dependent manner. These results establish a novel signaling process whereby PAK1 upregulates COX-2, reduces AEA and restricts tonic eCB-mediated processes. Because PAK1 and eCB are both critically involved in many other organ systems in addition to the brain, our findings may provide a unified mechanism by which PAK1 regulates these systems and their dysfunctions including cancers, inflammations and allergies. DOI: http://dx.doi.org/10.7554/eLife.14653.001 eLife Sciences Publications, Ltd 2016-06-14 /pmc/articles/PMC4907698/ /pubmed/27296803 http://dx.doi.org/10.7554/eLife.14653 Text en © 2016, Xia et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Xia, Shuting Zhou, Zikai Leung, Celeste Zhu, Yuehua Pan, Xingxiu Qi, Junxia Morena, Maria Hill, Matthew N Xie, Wei Jia, Zhengping p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title_full | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title_fullStr | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title_full_unstemmed | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title_short | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
title_sort | p21-activated kinase 1 restricts tonic endocannabinoid signaling in the hippocampus |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907698/ https://www.ncbi.nlm.nih.gov/pubmed/27296803 http://dx.doi.org/10.7554/eLife.14653 |
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