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In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans
Many neuronal groups such as dopamine-releasing (dopaminergic) neurons are functionally divergent, although the details of such divergence are not well understood. Dopamine in the nematode Caenorhabditis elegans modulates various neural functions and is released from four left-right pairs of neurons...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872038/ https://www.ncbi.nlm.nih.gov/pubmed/27193056 http://dx.doi.org/10.1038/srep26297 |
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author | Tanimoto, Yuki Zheng, Ying Grace Fei, Xianfeng Fujie, Yukako Hashimoto, Koichi Kimura, Koutarou D. |
author_facet | Tanimoto, Yuki Zheng, Ying Grace Fei, Xianfeng Fujie, Yukako Hashimoto, Koichi Kimura, Koutarou D. |
author_sort | Tanimoto, Yuki |
collection | PubMed |
description | Many neuronal groups such as dopamine-releasing (dopaminergic) neurons are functionally divergent, although the details of such divergence are not well understood. Dopamine in the nematode Caenorhabditis elegans modulates various neural functions and is released from four left-right pairs of neurons. The terminal identities of these dopaminergic neurons are regulated by the same genetic program, and previous studies have suggested that they are functionally redundant. In this study, however, we show functional divergence within the dopaminergic neurons of C. elegans. Because dopaminergic neurons of the animals were supposedly activated by mechanical stimulus upon entry into a lawn of their food bacteria, we developed a novel integrated microscope system that can auto-track a freely-moving (in actio) C. elegans to individually monitor and stimulate the neuronal activities of multiple neurons. We found that only head-dorsal pair of dopaminergic neurons (CEPD), but not head-ventral or posterior pairs, were preferentially activated upon food entry. In addition, the optogenetic activation of CEPD neurons alone exhibited effects similar to those observed upon food entry. Thus, our results demonstrated functional divergence in the genetically similar dopaminergic neurons, which may provide a new entry point toward understanding functional diversity of neurons beyond genetic terminal identification. |
format | Online Article Text |
id | pubmed-4872038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48720382016-06-01 In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans Tanimoto, Yuki Zheng, Ying Grace Fei, Xianfeng Fujie, Yukako Hashimoto, Koichi Kimura, Koutarou D. Sci Rep Article Many neuronal groups such as dopamine-releasing (dopaminergic) neurons are functionally divergent, although the details of such divergence are not well understood. Dopamine in the nematode Caenorhabditis elegans modulates various neural functions and is released from four left-right pairs of neurons. The terminal identities of these dopaminergic neurons are regulated by the same genetic program, and previous studies have suggested that they are functionally redundant. In this study, however, we show functional divergence within the dopaminergic neurons of C. elegans. Because dopaminergic neurons of the animals were supposedly activated by mechanical stimulus upon entry into a lawn of their food bacteria, we developed a novel integrated microscope system that can auto-track a freely-moving (in actio) C. elegans to individually monitor and stimulate the neuronal activities of multiple neurons. We found that only head-dorsal pair of dopaminergic neurons (CEPD), but not head-ventral or posterior pairs, were preferentially activated upon food entry. In addition, the optogenetic activation of CEPD neurons alone exhibited effects similar to those observed upon food entry. Thus, our results demonstrated functional divergence in the genetically similar dopaminergic neurons, which may provide a new entry point toward understanding functional diversity of neurons beyond genetic terminal identification. Nature Publishing Group 2016-05-19 /pmc/articles/PMC4872038/ /pubmed/27193056 http://dx.doi.org/10.1038/srep26297 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tanimoto, Yuki Zheng, Ying Grace Fei, Xianfeng Fujie, Yukako Hashimoto, Koichi Kimura, Koutarou D. In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title_full | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title_fullStr | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title_full_unstemmed | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title_short | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans |
title_sort | in actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872038/ https://www.ncbi.nlm.nih.gov/pubmed/27193056 http://dx.doi.org/10.1038/srep26297 |
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