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Functional architecture of neural circuits for leg proprioception in Drosophila
To effectively control their bodies, animals rely on feedback from proprioceptive mechanosensory neurons. In the Drosophila leg, different proprioceptor subtypes monitor joint position, movement direction, and vibration. Here, we investigate how these diverse sensory signals are integrated by centra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665017/ https://www.ncbi.nlm.nih.gov/pubmed/34637749 http://dx.doi.org/10.1016/j.cub.2021.09.035 |
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author | Chen, Chenghao Agrawal, Sweta Mark, Brandon Mamiya, Akira Sustar, Anne Phelps, Jasper S. Lee, Wei-Chung Allen Dickson, Barry J. Card, Gwyneth M. Tuthill, John C. |
author_facet | Chen, Chenghao Agrawal, Sweta Mark, Brandon Mamiya, Akira Sustar, Anne Phelps, Jasper S. Lee, Wei-Chung Allen Dickson, Barry J. Card, Gwyneth M. Tuthill, John C. |
author_sort | Chen, Chenghao |
collection | PubMed |
description | To effectively control their bodies, animals rely on feedback from proprioceptive mechanosensory neurons. In the Drosophila leg, different proprioceptor subtypes monitor joint position, movement direction, and vibration. Here, we investigate how these diverse sensory signals are integrated by central proprioceptive circuits. We find that signals for leg joint position and directional movement converge in second-order neurons, revealing pathways for local feedback control of leg posture. Distinct populations of second-order neurons integrate tibia vibration signals across pairs of legs, suggesting a role in detecting external substrate vibration. In each pathway, the flow of sensory information is dynamically gated and sculpted by inhibition. Overall, our results reveal parallel pathways for processing of internal and external mechanosensory signals, which we propose mediate feedback control of leg movement and vibration sensing, respectively. The existence of a functional connectivity map also provides a resource for interpreting connectomic reconstruction of neural circuits for leg proprioception. |
format | Online Article Text |
id | pubmed-8665017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-86650172021-12-11 Functional architecture of neural circuits for leg proprioception in Drosophila Chen, Chenghao Agrawal, Sweta Mark, Brandon Mamiya, Akira Sustar, Anne Phelps, Jasper S. Lee, Wei-Chung Allen Dickson, Barry J. Card, Gwyneth M. Tuthill, John C. Curr Biol Article To effectively control their bodies, animals rely on feedback from proprioceptive mechanosensory neurons. In the Drosophila leg, different proprioceptor subtypes monitor joint position, movement direction, and vibration. Here, we investigate how these diverse sensory signals are integrated by central proprioceptive circuits. We find that signals for leg joint position and directional movement converge in second-order neurons, revealing pathways for local feedback control of leg posture. Distinct populations of second-order neurons integrate tibia vibration signals across pairs of legs, suggesting a role in detecting external substrate vibration. In each pathway, the flow of sensory information is dynamically gated and sculpted by inhibition. Overall, our results reveal parallel pathways for processing of internal and external mechanosensory signals, which we propose mediate feedback control of leg movement and vibration sensing, respectively. The existence of a functional connectivity map also provides a resource for interpreting connectomic reconstruction of neural circuits for leg proprioception. 2021-10-11 2021-12-06 /pmc/articles/PMC8665017/ /pubmed/34637749 http://dx.doi.org/10.1016/j.cub.2021.09.035 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Chen, Chenghao Agrawal, Sweta Mark, Brandon Mamiya, Akira Sustar, Anne Phelps, Jasper S. Lee, Wei-Chung Allen Dickson, Barry J. Card, Gwyneth M. Tuthill, John C. Functional architecture of neural circuits for leg proprioception in Drosophila |
title | Functional architecture of neural circuits for leg proprioception in Drosophila |
title_full | Functional architecture of neural circuits for leg proprioception in Drosophila |
title_fullStr | Functional architecture of neural circuits for leg proprioception in Drosophila |
title_full_unstemmed | Functional architecture of neural circuits for leg proprioception in Drosophila |
title_short | Functional architecture of neural circuits for leg proprioception in Drosophila |
title_sort | functional architecture of neural circuits for leg proprioception in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665017/ https://www.ncbi.nlm.nih.gov/pubmed/34637749 http://dx.doi.org/10.1016/j.cub.2021.09.035 |
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