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Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior

The GPCR HCAR1 is known to be the sole receptor for lactate, which modulates its metabolic effects. Despite its significant role in many processes, mice deficient in HCAR1 exhibit no visible phenotype and are healthy and fertile. We performed transcriptomic analysis on HCAR1 deficient cells, in comb...

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Autores principales: Mohammad Nezhady, Mohammad Ali, Cagnone, Gael, Joyal, Jean-Sébastien, Chemtob, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634184/
https://www.ncbi.nlm.nih.gov/pubmed/37940970
http://dx.doi.org/10.1186/s12964-023-01188-z
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author Mohammad Nezhady, Mohammad Ali
Cagnone, Gael
Joyal, Jean-Sébastien
Chemtob, Sylvain
author_facet Mohammad Nezhady, Mohammad Ali
Cagnone, Gael
Joyal, Jean-Sébastien
Chemtob, Sylvain
author_sort Mohammad Nezhady, Mohammad Ali
collection PubMed
description The GPCR HCAR1 is known to be the sole receptor for lactate, which modulates its metabolic effects. Despite its significant role in many processes, mice deficient in HCAR1 exhibit no visible phenotype and are healthy and fertile. We performed transcriptomic analysis on HCAR1 deficient cells, in combination with lactate, to explore pathophysiologically altered processes. Processes such as immune regulation, various cancers, and neurodegenerative diseases were significantly enriched for HCAR1 transcriptomic signature. However, the most affected process of all was autism spectrum disorder. We performed behavioral tests on HCAR1 KO mice and observed that these mice manifest autistic-like behavior. Our data opens new avenues for research on HCAR1 and lactate effect at a pathological level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01188-z.
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spelling pubmed-106341842023-11-10 Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior Mohammad Nezhady, Mohammad Ali Cagnone, Gael Joyal, Jean-Sébastien Chemtob, Sylvain Cell Commun Signal Brief Report The GPCR HCAR1 is known to be the sole receptor for lactate, which modulates its metabolic effects. Despite its significant role in many processes, mice deficient in HCAR1 exhibit no visible phenotype and are healthy and fertile. We performed transcriptomic analysis on HCAR1 deficient cells, in combination with lactate, to explore pathophysiologically altered processes. Processes such as immune regulation, various cancers, and neurodegenerative diseases were significantly enriched for HCAR1 transcriptomic signature. However, the most affected process of all was autism spectrum disorder. We performed behavioral tests on HCAR1 KO mice and observed that these mice manifest autistic-like behavior. Our data opens new avenues for research on HCAR1 and lactate effect at a pathological level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01188-z. BioMed Central 2023-11-09 /pmc/articles/PMC10634184/ /pubmed/37940970 http://dx.doi.org/10.1186/s12964-023-01188-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Brief Report
Mohammad Nezhady, Mohammad Ali
Cagnone, Gael
Joyal, Jean-Sébastien
Chemtob, Sylvain
Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title_full Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title_fullStr Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title_full_unstemmed Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title_short Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior
title_sort lack of hcar1, the lactate gpcr, signaling promotes autistic-like behavior
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634184/
https://www.ncbi.nlm.nih.gov/pubmed/37940970
http://dx.doi.org/10.1186/s12964-023-01188-z
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