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Afferent Projections to Area Prostriata of the Mouse

Area prostriata plays important roles in fast detection and analysis of peripheral visual information. It remains unclear whether the prostriata directly receives and integrates information from other modalities. To gain insight into this issue, we investigated brain-wide afferent projections to mou...

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Autores principales: Hu, Jin-Meng, Chen, Chang-Hui, Chen, Sheng-Qiang, Ding, Song-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728849/
https://www.ncbi.nlm.nih.gov/pubmed/33328909
http://dx.doi.org/10.3389/fnana.2020.605021
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author Hu, Jin-Meng
Chen, Chang-Hui
Chen, Sheng-Qiang
Ding, Song-Lin
author_facet Hu, Jin-Meng
Chen, Chang-Hui
Chen, Sheng-Qiang
Ding, Song-Lin
author_sort Hu, Jin-Meng
collection PubMed
description Area prostriata plays important roles in fast detection and analysis of peripheral visual information. It remains unclear whether the prostriata directly receives and integrates information from other modalities. To gain insight into this issue, we investigated brain-wide afferent projections to mouse prostriata. We find convergent projections to layer 1 of the prostriata from primary and association visual and auditory cortices; retrosplenial, lateral entorhinal, and anterior cingulate cortices; subiculum; presubiculum; and anterior thalamic nuclei. Innervation of layers 2–3 of the prostriata mainly originates from the presubiculum (including postsubiculum) and anterior midline thalamic region. Layer 5 of the prostriata mainly receives its inputs from medial entorhinal, granular retrosplenial, and medial orbitofrontal cortices and anteromedial thalamic nucleus while layer 6 gets its major inputs from ectorhinal, postrhinal, and agranular retrosplenial cortices. The claustrum, locus coeruleus, and basal forebrain provide relatively diffuse innervation to the prostriata. Moreover, Cre-dependent tracing in cortical areas reveals that the cells of origin of the prostriata inputs are located in layers 2–4 and 5 of the neocortical areas, layers 2 and 5 of the medial entorhinal cortex, and layer 5 of the retrosplenial cortex. These results indicate that the prostriata is a unique region where primary and association visual and auditory inputs directly integrate with many limbic inputs.
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spelling pubmed-77288492020-12-15 Afferent Projections to Area Prostriata of the Mouse Hu, Jin-Meng Chen, Chang-Hui Chen, Sheng-Qiang Ding, Song-Lin Front Neuroanat Neuroscience Area prostriata plays important roles in fast detection and analysis of peripheral visual information. It remains unclear whether the prostriata directly receives and integrates information from other modalities. To gain insight into this issue, we investigated brain-wide afferent projections to mouse prostriata. We find convergent projections to layer 1 of the prostriata from primary and association visual and auditory cortices; retrosplenial, lateral entorhinal, and anterior cingulate cortices; subiculum; presubiculum; and anterior thalamic nuclei. Innervation of layers 2–3 of the prostriata mainly originates from the presubiculum (including postsubiculum) and anterior midline thalamic region. Layer 5 of the prostriata mainly receives its inputs from medial entorhinal, granular retrosplenial, and medial orbitofrontal cortices and anteromedial thalamic nucleus while layer 6 gets its major inputs from ectorhinal, postrhinal, and agranular retrosplenial cortices. The claustrum, locus coeruleus, and basal forebrain provide relatively diffuse innervation to the prostriata. Moreover, Cre-dependent tracing in cortical areas reveals that the cells of origin of the prostriata inputs are located in layers 2–4 and 5 of the neocortical areas, layers 2 and 5 of the medial entorhinal cortex, and layer 5 of the retrosplenial cortex. These results indicate that the prostriata is a unique region where primary and association visual and auditory inputs directly integrate with many limbic inputs. Frontiers Media S.A. 2020-11-27 /pmc/articles/PMC7728849/ /pubmed/33328909 http://dx.doi.org/10.3389/fnana.2020.605021 Text en Copyright © 2020 Hu, Chen, Chen and Ding. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Hu, Jin-Meng
Chen, Chang-Hui
Chen, Sheng-Qiang
Ding, Song-Lin
Afferent Projections to Area Prostriata of the Mouse
title Afferent Projections to Area Prostriata of the Mouse
title_full Afferent Projections to Area Prostriata of the Mouse
title_fullStr Afferent Projections to Area Prostriata of the Mouse
title_full_unstemmed Afferent Projections to Area Prostriata of the Mouse
title_short Afferent Projections to Area Prostriata of the Mouse
title_sort afferent projections to area prostriata of the mouse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728849/
https://www.ncbi.nlm.nih.gov/pubmed/33328909
http://dx.doi.org/10.3389/fnana.2020.605021
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