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Neural bases of self‐ and object‐motion in a naturalistic vision

To plan movements toward objects our brain must recognize whether retinal displacement is due to self‐motion and/or to object‐motion. Here, we aimed to test whether motion areas are able to segregate these types of motion. We combined an event‐related functional magnetic resonance imaging experiment...

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Autores principales: Pitzalis, Sabrina, Serra, Chiara, Sulpizio, Valentina, Committeri, Giorgia, de Pasquale, Francesco, Fattori, Patrizia, Galletti, Claudio, Sepe, Rosamaria, Galati, Gaspare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267932/
https://www.ncbi.nlm.nih.gov/pubmed/31713304
http://dx.doi.org/10.1002/hbm.24862
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author Pitzalis, Sabrina
Serra, Chiara
Sulpizio, Valentina
Committeri, Giorgia
de Pasquale, Francesco
Fattori, Patrizia
Galletti, Claudio
Sepe, Rosamaria
Galati, Gaspare
author_facet Pitzalis, Sabrina
Serra, Chiara
Sulpizio, Valentina
Committeri, Giorgia
de Pasquale, Francesco
Fattori, Patrizia
Galletti, Claudio
Sepe, Rosamaria
Galati, Gaspare
author_sort Pitzalis, Sabrina
collection PubMed
description To plan movements toward objects our brain must recognize whether retinal displacement is due to self‐motion and/or to object‐motion. Here, we aimed to test whether motion areas are able to segregate these types of motion. We combined an event‐related functional magnetic resonance imaging experiment, brain mapping techniques, and wide‐field stimulation to study the responsivity of motion‐sensitive areas to pure and combined self‐ and object‐motion conditions during virtual movies of a train running within a realistic landscape. We observed a selective response in MT to the pure object‐motion condition, and in medial (PEc, pCi, CSv, and CMA) and lateral (PIC and LOR) areas to the pure self‐motion condition. Some other regions (like V6) responded more to complex visual stimulation where both object‐ and self‐motion were present. Among all, we found that some motion regions (V3A, LOR, MT, V6, and IPSmot) could extract object‐motion information from the overall motion, recognizing the real movement of the train even when the images remain still (on the screen), or moved, because of self‐movements. We propose that these motion areas might be good candidates for the “flow parsing mechanism,” that is the capability to extract object‐motion information from retinal motion signals by subtracting out the optic flow components.
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spelling pubmed-72679322020-06-12 Neural bases of self‐ and object‐motion in a naturalistic vision Pitzalis, Sabrina Serra, Chiara Sulpizio, Valentina Committeri, Giorgia de Pasquale, Francesco Fattori, Patrizia Galletti, Claudio Sepe, Rosamaria Galati, Gaspare Hum Brain Mapp Research Articles To plan movements toward objects our brain must recognize whether retinal displacement is due to self‐motion and/or to object‐motion. Here, we aimed to test whether motion areas are able to segregate these types of motion. We combined an event‐related functional magnetic resonance imaging experiment, brain mapping techniques, and wide‐field stimulation to study the responsivity of motion‐sensitive areas to pure and combined self‐ and object‐motion conditions during virtual movies of a train running within a realistic landscape. We observed a selective response in MT to the pure object‐motion condition, and in medial (PEc, pCi, CSv, and CMA) and lateral (PIC and LOR) areas to the pure self‐motion condition. Some other regions (like V6) responded more to complex visual stimulation where both object‐ and self‐motion were present. Among all, we found that some motion regions (V3A, LOR, MT, V6, and IPSmot) could extract object‐motion information from the overall motion, recognizing the real movement of the train even when the images remain still (on the screen), or moved, because of self‐movements. We propose that these motion areas might be good candidates for the “flow parsing mechanism,” that is the capability to extract object‐motion information from retinal motion signals by subtracting out the optic flow components. John Wiley & Sons, Inc. 2019-11-11 /pmc/articles/PMC7267932/ /pubmed/31713304 http://dx.doi.org/10.1002/hbm.24862 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Pitzalis, Sabrina
Serra, Chiara
Sulpizio, Valentina
Committeri, Giorgia
de Pasquale, Francesco
Fattori, Patrizia
Galletti, Claudio
Sepe, Rosamaria
Galati, Gaspare
Neural bases of self‐ and object‐motion in a naturalistic vision
title Neural bases of self‐ and object‐motion in a naturalistic vision
title_full Neural bases of self‐ and object‐motion in a naturalistic vision
title_fullStr Neural bases of self‐ and object‐motion in a naturalistic vision
title_full_unstemmed Neural bases of self‐ and object‐motion in a naturalistic vision
title_short Neural bases of self‐ and object‐motion in a naturalistic vision
title_sort neural bases of self‐ and object‐motion in a naturalistic vision
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267932/
https://www.ncbi.nlm.nih.gov/pubmed/31713304
http://dx.doi.org/10.1002/hbm.24862
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