Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783621357492240384 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7728849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hujinmeng afferentprojectionstoareaprostriataofthemouse AT chenchanghui afferentprojectionstoareaprostriataofthemouse AT chenshengqiang afferentprojectionstoareaprostriataofthemouse AT dingsonglin afferentprojectionstoareaprostriataofthemouse |