Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice

Abstract Lamellipodin (Lpd) functions as an important signalling integrator downstream of growth factor and axon guidance receptors. Mechanistically, Lpd promotes actin polymerization by interacting with F-actin and the actin effectors Ena/VASP proteins and the SCAR/WAVE complex. Thereby, Lpd suppor...

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Autores principales: Cristian Bodo, Cathy Fernandes, Matthias Krause
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/602c36a7f5d1499a9eb0309abd188dfd
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spelling oai:doaj.org-article:602c36a7f5d1499a9eb0309abd188dfd2021-12-02T11:40:30ZBrain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice10.1038/s41598-017-05043-32045-2322https://doaj.org/article/602c36a7f5d1499a9eb0309abd188dfd2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-05043-3https://doaj.org/toc/2045-2322Abstract Lamellipodin (Lpd) functions as an important signalling integrator downstream of growth factor and axon guidance receptors. Mechanistically, Lpd promotes actin polymerization by interacting with F-actin and the actin effectors Ena/VASP proteins and the SCAR/WAVE complex. Thereby, Lpd supports lamellipodia protrusion, cell migration and endocytosis. In the mammalian central nervous system, Lpd contributes to neuronal morphogenesis, neuronal migration during development and its C. elegans orthologue MIG-10 also supports synaptogenesis. However, the consequences of loss of Lpd in the CNS on behaviour are unknown. In our current study, we crossed our Lpd conditional knockout mice with a mouse line expressing Cre under the CNS specific Nestin promoter to restrict the genetic ablation of Lpd to the central nervous system. Detailed behavioural analysis of the resulting Nestin-Cre-Lpd knockout mouse line revealed a specific behavioural phenotype characterised by hyperactivity and increased anxiety.Cristian BodoCathy FernandesMatthias KrauseNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Cristian Bodo
Cathy Fernandes
Matthias Krause
Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
description Abstract Lamellipodin (Lpd) functions as an important signalling integrator downstream of growth factor and axon guidance receptors. Mechanistically, Lpd promotes actin polymerization by interacting with F-actin and the actin effectors Ena/VASP proteins and the SCAR/WAVE complex. Thereby, Lpd supports lamellipodia protrusion, cell migration and endocytosis. In the mammalian central nervous system, Lpd contributes to neuronal morphogenesis, neuronal migration during development and its C. elegans orthologue MIG-10 also supports synaptogenesis. However, the consequences of loss of Lpd in the CNS on behaviour are unknown. In our current study, we crossed our Lpd conditional knockout mice with a mouse line expressing Cre under the CNS specific Nestin promoter to restrict the genetic ablation of Lpd to the central nervous system. Detailed behavioural analysis of the resulting Nestin-Cre-Lpd knockout mouse line revealed a specific behavioural phenotype characterised by hyperactivity and increased anxiety.
format article
author Cristian Bodo
Cathy Fernandes
Matthias Krause
author_facet Cristian Bodo
Cathy Fernandes
Matthias Krause
author_sort Cristian Bodo
title Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
title_short Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
title_full Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
title_fullStr Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
title_full_unstemmed Brain specific Lamellipodin knockout results in hyperactivity and increased anxiety of mice
title_sort brain specific lamellipodin knockout results in hyperactivity and increased anxiety of mice
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/602c36a7f5d1499a9eb0309abd188dfd
work_keys_str_mv AT cristianbodo brainspecificlamellipodinknockoutresultsinhyperactivityandincreasedanxietyofmice
AT cathyfernandes brainspecificlamellipodinknockoutresultsinhyperactivityandincreasedanxietyofmice
AT matthiaskrause brainspecificlamellipodinknockoutresultsinhyperactivityandincreasedanxietyofmice
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