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Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse
Mitochondrial dysfunction is strongly associated with autism spectrum disorder (ASD) and the Inner mitochondrial membrane protein 2-like (IMMP2L) gene is linked to autism inheritance. However, the biological basis of this linkage is unknown notwithstanding independent reports of oxidative stress in...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531238/ https://www.ncbi.nlm.nih.gov/pubmed/37761857 http://dx.doi.org/10.3390/genes14091717 |
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author | Lawther, Adam J. Zieba, Jerzy Fang, Zhiming Furlong, Teri M. Conn, Illya Govindaraju, Hemna Choong, Laura L. Y. Turner, Nigel Siddiqui, Khawar Sohail Bridge, Wallace Merlin, Sam Hyams, Tzipi Cohen Killingsworth, Murray Eapen, Valsamma Clarke, Raymond A. Walker, Adam K. |
author_facet | Lawther, Adam J. Zieba, Jerzy Fang, Zhiming Furlong, Teri M. Conn, Illya Govindaraju, Hemna Choong, Laura L. Y. Turner, Nigel Siddiqui, Khawar Sohail Bridge, Wallace Merlin, Sam Hyams, Tzipi Cohen Killingsworth, Murray Eapen, Valsamma Clarke, Raymond A. Walker, Adam K. |
author_sort | Lawther, Adam J. |
collection | PubMed |
description | Mitochondrial dysfunction is strongly associated with autism spectrum disorder (ASD) and the Inner mitochondrial membrane protein 2-like (IMMP2L) gene is linked to autism inheritance. However, the biological basis of this linkage is unknown notwithstanding independent reports of oxidative stress in association with both IMMP2L and ASD. To better understand IMMP2L’s association with behaviour, we developed the Immp2l(KD) knockout (KO) mouse model which is devoid of Immp2l peptidase activity. Immp2l(KD) −/− KO mice do not display any of the core behavioural symptoms of ASD, albeit homozygous Immp2l(KD) −/− KO mice do display increased auditory stimulus-driven instrumental behaviour and increased amphetamine-induced locomotion. Due to reports of increased ROS and oxidative stress phenotypes in an earlier truncated Immp2l mouse model resulting from an intragenic deletion within Immp2l, we tested whether high doses of the synthetic mitochondrial targeted antioxidant (MitoQ) could reverse or moderate the behavioural changes in Immp2l(KD) −/− KO mice. To our surprise, we observed that ROS levels were not increased but significantly lowered in our new Immp2l(KD) −/− KO mice and that these mice had no oxidative stress-associated phenotypes and were fully fertile with no age-related ataxia or neurodegeneration as ascertained using electron microscopy. Furthermore, the antioxidant MitoQ had no effect on the increased amphetamine-induced locomotion of these mice. Together, these findings indicate that the behavioural changes in Immp2l(KD) −/− KO mice are associated with an antioxidant-like phenotype with lowered and not increased levels of ROS and no oxidative stress-related phenotypes. This suggested that treatments with antioxidants are unlikely to be effective in treating behaviours directly resulting from the loss of Immp2l/IMMP2L activity, while any behavioural deficits that maybe associated with IMMP2L intragenic deletion-associated truncations have yet to be determined. |
format | Online Article Text |
id | pubmed-10531238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105312382023-09-28 Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse Lawther, Adam J. Zieba, Jerzy Fang, Zhiming Furlong, Teri M. Conn, Illya Govindaraju, Hemna Choong, Laura L. Y. Turner, Nigel Siddiqui, Khawar Sohail Bridge, Wallace Merlin, Sam Hyams, Tzipi Cohen Killingsworth, Murray Eapen, Valsamma Clarke, Raymond A. Walker, Adam K. Genes (Basel) Article Mitochondrial dysfunction is strongly associated with autism spectrum disorder (ASD) and the Inner mitochondrial membrane protein 2-like (IMMP2L) gene is linked to autism inheritance. However, the biological basis of this linkage is unknown notwithstanding independent reports of oxidative stress in association with both IMMP2L and ASD. To better understand IMMP2L’s association with behaviour, we developed the Immp2l(KD) knockout (KO) mouse model which is devoid of Immp2l peptidase activity. Immp2l(KD) −/− KO mice do not display any of the core behavioural symptoms of ASD, albeit homozygous Immp2l(KD) −/− KO mice do display increased auditory stimulus-driven instrumental behaviour and increased amphetamine-induced locomotion. Due to reports of increased ROS and oxidative stress phenotypes in an earlier truncated Immp2l mouse model resulting from an intragenic deletion within Immp2l, we tested whether high doses of the synthetic mitochondrial targeted antioxidant (MitoQ) could reverse or moderate the behavioural changes in Immp2l(KD) −/− KO mice. To our surprise, we observed that ROS levels were not increased but significantly lowered in our new Immp2l(KD) −/− KO mice and that these mice had no oxidative stress-associated phenotypes and were fully fertile with no age-related ataxia or neurodegeneration as ascertained using electron microscopy. Furthermore, the antioxidant MitoQ had no effect on the increased amphetamine-induced locomotion of these mice. Together, these findings indicate that the behavioural changes in Immp2l(KD) −/− KO mice are associated with an antioxidant-like phenotype with lowered and not increased levels of ROS and no oxidative stress-related phenotypes. This suggested that treatments with antioxidants are unlikely to be effective in treating behaviours directly resulting from the loss of Immp2l/IMMP2L activity, while any behavioural deficits that maybe associated with IMMP2L intragenic deletion-associated truncations have yet to be determined. MDPI 2023-08-28 /pmc/articles/PMC10531238/ /pubmed/37761857 http://dx.doi.org/10.3390/genes14091717 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lawther, Adam J. Zieba, Jerzy Fang, Zhiming Furlong, Teri M. Conn, Illya Govindaraju, Hemna Choong, Laura L. Y. Turner, Nigel Siddiqui, Khawar Sohail Bridge, Wallace Merlin, Sam Hyams, Tzipi Cohen Killingsworth, Murray Eapen, Valsamma Clarke, Raymond A. Walker, Adam K. Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title | Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title_full | Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title_fullStr | Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title_full_unstemmed | Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title_short | Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse |
title_sort | antioxidant behavioural phenotype in the immp2l gene knock-out mouse |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531238/ https://www.ncbi.nlm.nih.gov/pubmed/37761857 http://dx.doi.org/10.3390/genes14091717 |
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