Cargando…
Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus
In order to explore and interact with their surroundings, animals need to orient toward specific positions in space. Throughout the animal kingdom, head movements represent a primary form of orienting behavior. The superior colliculus (SC) is a fundamental structure for the generation of orienting r...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739420/ https://www.ncbi.nlm.nih.gov/pubmed/31474533 http://dx.doi.org/10.1016/j.cub.2019.07.083 |
_version_ | 1783450941813424128 |
---|---|
author | Masullo, Laura Mariotti, Letizia Alexandre, Nicolas Freire-Pritchett, Paula Boulanger, Jerome Tripodi, Marco |
author_facet | Masullo, Laura Mariotti, Letizia Alexandre, Nicolas Freire-Pritchett, Paula Boulanger, Jerome Tripodi, Marco |
author_sort | Masullo, Laura |
collection | PubMed |
description | In order to explore and interact with their surroundings, animals need to orient toward specific positions in space. Throughout the animal kingdom, head movements represent a primary form of orienting behavior. The superior colliculus (SC) is a fundamental structure for the generation of orienting responses, but how genetically distinct groups of collicular neurons contribute to these spatially tuned behaviors remains largely to be defined. Here, through the genetic dissection of the murine SC, we identify a functionally and genetically homogeneous subclass of glutamatergic neurons defined by the expression of the paired-like homeodomain transcription factor Pitx2. We show that the optogenetic stimulation of Pitx2(ON) neurons drives three-dimensional head displacements characterized by stepwise, saccade-like kinematics. Furthermore, during naturalistic foraging behavior, the activity of Pitx2(ON) neurons precedes and predicts the onset of spatially tuned head movements. Intriguingly, we reveal that Pitx2(ON) neurons are clustered in an orderly array of anatomical modules that tile the entire intermediate layer of the SC. Such a modular organization gives origin to a discrete and discontinuous representation of the motor space, with each Pitx2(ON) module subtending a defined portion of the animal’s egocentric space. The modularity of Pitx2(ON) neurons provides an anatomical substrate for the convergence of spatially coherent sensory and motor signals of cortical and subcortical origins, thereby promoting the recruitment of appropriate movement vectors. Overall, these data support the view of the superior colliculus as a selectively addressable and modularly organized spatial-motor register. |
format | Online Article Text |
id | pubmed-6739420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67394202019-09-16 Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus Masullo, Laura Mariotti, Letizia Alexandre, Nicolas Freire-Pritchett, Paula Boulanger, Jerome Tripodi, Marco Curr Biol Article In order to explore and interact with their surroundings, animals need to orient toward specific positions in space. Throughout the animal kingdom, head movements represent a primary form of orienting behavior. The superior colliculus (SC) is a fundamental structure for the generation of orienting responses, but how genetically distinct groups of collicular neurons contribute to these spatially tuned behaviors remains largely to be defined. Here, through the genetic dissection of the murine SC, we identify a functionally and genetically homogeneous subclass of glutamatergic neurons defined by the expression of the paired-like homeodomain transcription factor Pitx2. We show that the optogenetic stimulation of Pitx2(ON) neurons drives three-dimensional head displacements characterized by stepwise, saccade-like kinematics. Furthermore, during naturalistic foraging behavior, the activity of Pitx2(ON) neurons precedes and predicts the onset of spatially tuned head movements. Intriguingly, we reveal that Pitx2(ON) neurons are clustered in an orderly array of anatomical modules that tile the entire intermediate layer of the SC. Such a modular organization gives origin to a discrete and discontinuous representation of the motor space, with each Pitx2(ON) module subtending a defined portion of the animal’s egocentric space. The modularity of Pitx2(ON) neurons provides an anatomical substrate for the convergence of spatially coherent sensory and motor signals of cortical and subcortical origins, thereby promoting the recruitment of appropriate movement vectors. Overall, these data support the view of the superior colliculus as a selectively addressable and modularly organized spatial-motor register. Cell Press 2019-09-09 /pmc/articles/PMC6739420/ /pubmed/31474533 http://dx.doi.org/10.1016/j.cub.2019.07.083 Text en © 2019 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Masullo, Laura Mariotti, Letizia Alexandre, Nicolas Freire-Pritchett, Paula Boulanger, Jerome Tripodi, Marco Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title | Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title_full | Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title_fullStr | Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title_full_unstemmed | Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title_short | Genetically Defined Functional Modules for Spatial Orienting in the Mouse Superior Colliculus |
title_sort | genetically defined functional modules for spatial orienting in the mouse superior colliculus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739420/ https://www.ncbi.nlm.nih.gov/pubmed/31474533 http://dx.doi.org/10.1016/j.cub.2019.07.083 |
work_keys_str_mv | AT masullolaura geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus AT mariottiletizia geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus AT alexandrenicolas geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus AT freirepritchettpaula geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus AT boulangerjerome geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus AT tripodimarco geneticallydefinedfunctionalmodulesforspatialorientinginthemousesuperiorcolliculus |