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Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain

Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons....

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Autores principales: Marin, Elizabeth C., Büld, Laurin, Theiss, Maria, Sarkissian, Tatevik, Roberts, Ruairí J.V., Turnbull, Robert, Tamimi, Imaan F.M., Pleijzier, Markus W., Laursen, Willem J., Drummond, Nik, Schlegel, Philipp, Bates, Alexander S., Li, Feng, Landgraf, Matthias, Costa, Marta, Bock, Davi D., Garrity, Paul A., Jefferis, Gregory S.X.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443704/
https://www.ncbi.nlm.nih.gov/pubmed/32619476
http://dx.doi.org/10.1016/j.cub.2020.06.028
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author Marin, Elizabeth C.
Büld, Laurin
Theiss, Maria
Sarkissian, Tatevik
Roberts, Ruairí J.V.
Turnbull, Robert
Tamimi, Imaan F.M.
Pleijzier, Markus W.
Laursen, Willem J.
Drummond, Nik
Schlegel, Philipp
Bates, Alexander S.
Li, Feng
Landgraf, Matthias
Costa, Marta
Bock, Davi D.
Garrity, Paul A.
Jefferis, Gregory S.X.E.
author_facet Marin, Elizabeth C.
Büld, Laurin
Theiss, Maria
Sarkissian, Tatevik
Roberts, Ruairí J.V.
Turnbull, Robert
Tamimi, Imaan F.M.
Pleijzier, Markus W.
Laursen, Willem J.
Drummond, Nik
Schlegel, Philipp
Bates, Alexander S.
Li, Feng
Landgraf, Matthias
Costa, Marta
Bock, Davi D.
Garrity, Paul A.
Jefferis, Gregory S.X.E.
author_sort Marin, Elizabeth C.
collection PubMed
description Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons. We have identified two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay thermo- and hygrosensory information to higher brain centers, including the mushroom body and lateral horn, seats of learned and innate behavior. We present the first connectome of a thermo- and hygrosensory neuropil, the lateral accessory calyx (lACA), by reconstructing neurons downstream of heating- and cooling-responsive VP PNs. A few mushroom body-intrinsic neurons solely receive thermosensory input from the lACA, while most receive additional olfactory and thermo- and/or hygrosensory PN inputs. Furthermore, several classes of lACA-associated neurons form a local network with outputs to other brain neuropils, suggesting that the lACA serves as a hub for thermo- and hygrosensory circuitry. For example, DN1a neurons link thermosensory PNs in the lACA to the circadian clock via the accessory medulla. Finally, we survey strongly connected downstream partners of VP PNs across the protocerebrum; these include a descending neuron targeted by dry-responsive VP PNs, meaning that just two synapses might separate hygrosensory inputs from motor circuits. These data provide a comprehensive first- and second-order layer analysis of Drosophila thermo- and hygrosensory systems and an initial survey of third-order neurons that could directly modulate behavior.
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spelling pubmed-74437042020-08-28 Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain Marin, Elizabeth C. Büld, Laurin Theiss, Maria Sarkissian, Tatevik Roberts, Ruairí J.V. Turnbull, Robert Tamimi, Imaan F.M. Pleijzier, Markus W. Laursen, Willem J. Drummond, Nik Schlegel, Philipp Bates, Alexander S. Li, Feng Landgraf, Matthias Costa, Marta Bock, Davi D. Garrity, Paul A. Jefferis, Gregory S.X.E. Curr Biol Article Animals exhibit innate and learned preferences for temperature and humidity—conditions critical for their survival and reproduction. Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antennal thermo- and hygrosensory neurons. We have identified two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay thermo- and hygrosensory information to higher brain centers, including the mushroom body and lateral horn, seats of learned and innate behavior. We present the first connectome of a thermo- and hygrosensory neuropil, the lateral accessory calyx (lACA), by reconstructing neurons downstream of heating- and cooling-responsive VP PNs. A few mushroom body-intrinsic neurons solely receive thermosensory input from the lACA, while most receive additional olfactory and thermo- and/or hygrosensory PN inputs. Furthermore, several classes of lACA-associated neurons form a local network with outputs to other brain neuropils, suggesting that the lACA serves as a hub for thermo- and hygrosensory circuitry. For example, DN1a neurons link thermosensory PNs in the lACA to the circadian clock via the accessory medulla. Finally, we survey strongly connected downstream partners of VP PNs across the protocerebrum; these include a descending neuron targeted by dry-responsive VP PNs, meaning that just two synapses might separate hygrosensory inputs from motor circuits. These data provide a comprehensive first- and second-order layer analysis of Drosophila thermo- and hygrosensory systems and an initial survey of third-order neurons that could directly modulate behavior. Cell Press 2020-08-17 /pmc/articles/PMC7443704/ /pubmed/32619476 http://dx.doi.org/10.1016/j.cub.2020.06.028 Text en © 2020 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marin, Elizabeth C.
Büld, Laurin
Theiss, Maria
Sarkissian, Tatevik
Roberts, Ruairí J.V.
Turnbull, Robert
Tamimi, Imaan F.M.
Pleijzier, Markus W.
Laursen, Willem J.
Drummond, Nik
Schlegel, Philipp
Bates, Alexander S.
Li, Feng
Landgraf, Matthias
Costa, Marta
Bock, Davi D.
Garrity, Paul A.
Jefferis, Gregory S.X.E.
Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title_full Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title_fullStr Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title_full_unstemmed Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title_short Connectomics Analysis Reveals First-, Second-, and Third-Order Thermosensory and Hygrosensory Neurons in the Adult Drosophila Brain
title_sort connectomics analysis reveals first-, second-, and third-order thermosensory and hygrosensory neurons in the adult drosophila brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443704/
https://www.ncbi.nlm.nih.gov/pubmed/32619476
http://dx.doi.org/10.1016/j.cub.2020.06.028
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