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Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice
Animals respond to environmental threats, e.g. looming visual stimuli, with innate defensive behaviors such as escape and freezing. The key neural circuits that participate in the generation of such dimorphic defensive behaviors remain unclear. Here we show that the dimorphic behavioral patterns tri...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964329/ https://www.ncbi.nlm.nih.gov/pubmed/29581428 http://dx.doi.org/10.1038/s41467-018-03580-7 |
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author | Shang, Congping Chen, Zijun Liu, Aixue Li, Yang Zhang, Jiajing Qu, Baole Yan, Fei Zhang, Yaning Liu, Weixiu Liu, Zhihui Guo, Xiaofei Li, Dapeng Wang, Yi Cao, Peng |
author_facet | Shang, Congping Chen, Zijun Liu, Aixue Li, Yang Zhang, Jiajing Qu, Baole Yan, Fei Zhang, Yaning Liu, Weixiu Liu, Zhihui Guo, Xiaofei Li, Dapeng Wang, Yi Cao, Peng |
author_sort | Shang, Congping |
collection | PubMed |
description | Animals respond to environmental threats, e.g. looming visual stimuli, with innate defensive behaviors such as escape and freezing. The key neural circuits that participate in the generation of such dimorphic defensive behaviors remain unclear. Here we show that the dimorphic behavioral patterns triggered by looming visual stimuli are mediated by parvalbumin-positive (PV(+)) projection neurons in mouse superior colliculus (SC). Two distinct groups of SC PV(+) neurons form divergent pathways to transmit threat-relevant visual signals to neurons in the parabigeminal nucleus (PBGN) and lateral posterior thalamic nucleus (LPTN). Activations of PV(+) SC-PBGN and SC-LPTN pathways mimic the dimorphic defensive behaviors. The PBGN and LPTN neurons are co-activated by looming visual stimuli. Bilateral inactivation of either nucleus results in the defensive behavior dominated by the other nucleus. Together, these data suggest that the SC orchestrates dimorphic defensive behaviors through two separate tectofugal pathways that may have interactions. |
format | Online Article Text |
id | pubmed-5964329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59643292018-05-24 Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice Shang, Congping Chen, Zijun Liu, Aixue Li, Yang Zhang, Jiajing Qu, Baole Yan, Fei Zhang, Yaning Liu, Weixiu Liu, Zhihui Guo, Xiaofei Li, Dapeng Wang, Yi Cao, Peng Nat Commun Article Animals respond to environmental threats, e.g. looming visual stimuli, with innate defensive behaviors such as escape and freezing. The key neural circuits that participate in the generation of such dimorphic defensive behaviors remain unclear. Here we show that the dimorphic behavioral patterns triggered by looming visual stimuli are mediated by parvalbumin-positive (PV(+)) projection neurons in mouse superior colliculus (SC). Two distinct groups of SC PV(+) neurons form divergent pathways to transmit threat-relevant visual signals to neurons in the parabigeminal nucleus (PBGN) and lateral posterior thalamic nucleus (LPTN). Activations of PV(+) SC-PBGN and SC-LPTN pathways mimic the dimorphic defensive behaviors. The PBGN and LPTN neurons are co-activated by looming visual stimuli. Bilateral inactivation of either nucleus results in the defensive behavior dominated by the other nucleus. Together, these data suggest that the SC orchestrates dimorphic defensive behaviors through two separate tectofugal pathways that may have interactions. Nature Publishing Group UK 2018-03-26 /pmc/articles/PMC5964329/ /pubmed/29581428 http://dx.doi.org/10.1038/s41467-018-03580-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shang, Congping Chen, Zijun Liu, Aixue Li, Yang Zhang, Jiajing Qu, Baole Yan, Fei Zhang, Yaning Liu, Weixiu Liu, Zhihui Guo, Xiaofei Li, Dapeng Wang, Yi Cao, Peng Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title | Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title_full | Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title_fullStr | Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title_full_unstemmed | Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title_short | Divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
title_sort | divergent midbrain circuits orchestrate escape and freezing responses to looming stimuli in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964329/ https://www.ncbi.nlm.nih.gov/pubmed/29581428 http://dx.doi.org/10.1038/s41467-018-03580-7 |
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