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Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice
Neuronal calcium sensor 1 (NCS1) regulates a wide range of cellular functions throughout the mammalian nervous systems. Altered NCS1 expression is associated with neurodevelopmental and neurodegenerative diseases. Previous studies focused on affective and cognitive behaviors in NCS1 knockout (KO) mi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840744/ https://www.ncbi.nlm.nih.gov/pubmed/33504822 http://dx.doi.org/10.1038/s41598-021-81650-5 |
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author | Nguyen, Lien D. Nolte, Luca G. Tan, Winston J. T. Giuvelis, Denise Santos-Sacchi, Joseph Bilsky, Edward Ehrlich, Barbara E. |
author_facet | Nguyen, Lien D. Nolte, Luca G. Tan, Winston J. T. Giuvelis, Denise Santos-Sacchi, Joseph Bilsky, Edward Ehrlich, Barbara E. |
author_sort | Nguyen, Lien D. |
collection | PubMed |
description | Neuronal calcium sensor 1 (NCS1) regulates a wide range of cellular functions throughout the mammalian nervous systems. Altered NCS1 expression is associated with neurodevelopmental and neurodegenerative diseases. Previous studies focused on affective and cognitive behaviors in NCS1 knockout (KO) mice, but little is known about the physiological and pathological states associated with the loss of NCS1 in the peripheral nervous system. We previously reported that NCS1 expression was reduced following paclitaxel-induced peripheral neuropathy. Here, we comprehensively investigated the phenotypes of NCS1-KO mice through a battery of behavioral tests examining both central and peripheral nervous systems. Generally, only mild differences were observed in thermal sensation and memory acquisition between NCS1-WT and -KO male mice, but not in female mice. No differences were observed in motor performance, affective behaviors, and hearing in both sexes. These results suggest that NCS1 plays a modulatory role in sensory perceptions and cognition, particularly in male mice. NCS1 has been proposed as a pharmacological target for various diseases. Therefore, the sex-specific effects of NCS1 loss may be of clinical interest. As we examined a constitutive KO model, future studies focusing on various conditional KO models will further elucidate the precise physiological significance of NCS1. |
format | Online Article Text |
id | pubmed-7840744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78407442021-01-28 Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice Nguyen, Lien D. Nolte, Luca G. Tan, Winston J. T. Giuvelis, Denise Santos-Sacchi, Joseph Bilsky, Edward Ehrlich, Barbara E. Sci Rep Article Neuronal calcium sensor 1 (NCS1) regulates a wide range of cellular functions throughout the mammalian nervous systems. Altered NCS1 expression is associated with neurodevelopmental and neurodegenerative diseases. Previous studies focused on affective and cognitive behaviors in NCS1 knockout (KO) mice, but little is known about the physiological and pathological states associated with the loss of NCS1 in the peripheral nervous system. We previously reported that NCS1 expression was reduced following paclitaxel-induced peripheral neuropathy. Here, we comprehensively investigated the phenotypes of NCS1-KO mice through a battery of behavioral tests examining both central and peripheral nervous systems. Generally, only mild differences were observed in thermal sensation and memory acquisition between NCS1-WT and -KO male mice, but not in female mice. No differences were observed in motor performance, affective behaviors, and hearing in both sexes. These results suggest that NCS1 plays a modulatory role in sensory perceptions and cognition, particularly in male mice. NCS1 has been proposed as a pharmacological target for various diseases. Therefore, the sex-specific effects of NCS1 loss may be of clinical interest. As we examined a constitutive KO model, future studies focusing on various conditional KO models will further elucidate the precise physiological significance of NCS1. Nature Publishing Group UK 2021-01-27 /pmc/articles/PMC7840744/ /pubmed/33504822 http://dx.doi.org/10.1038/s41598-021-81650-5 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Nguyen, Lien D. Nolte, Luca G. Tan, Winston J. T. Giuvelis, Denise Santos-Sacchi, Joseph Bilsky, Edward Ehrlich, Barbara E. Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title | Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title_full | Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title_fullStr | Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title_full_unstemmed | Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title_short | Comprehensive somatosensory and neurological phenotyping of NCS1 knockout mice |
title_sort | comprehensive somatosensory and neurological phenotyping of ncs1 knockout mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840744/ https://www.ncbi.nlm.nih.gov/pubmed/33504822 http://dx.doi.org/10.1038/s41598-021-81650-5 |
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