Cholinergic signaling at the body wall neuromuscular junction distally inhibits feeding behavior in Caenorhabditis elegans
Cholinergic signaling at the body wall neuromuscular junction distally inhibits feeding behavior in Caenorhabditis elegans
Complex biological functions within organisms are frequently orchestrated by systemic communication between tissues. In the model organism Caenorhabditis elegans, the pharyngeal and body wall neuromuscular junctions are two discrete structures that control feeding and locomotion, respectively. Separate, the well-defined neuromuscular circuits control these distinct tissues. Nonetheless, the emergent behaviors, feeding and locomotion, are coordinated to guarantee the efficiency of food intake. Here, we show that pharmacological hyperactivation of cholinergic transmission at the body wall muscle reduces the rate of pumping behavior. This was evidenced by a systematic screening of the effect of the cholinesterase inhibitor aldicarb on the rate of pharyngeal pumping on food in mutant worms. The screening revealed that the key determinants of the inhibitory effect of aldicarb on pharyngeal pumping are located at the body wall neuromuscular junction. In fact, the selective stimulation of the body wall muscle receptors with the agonist levamisole inhibited pumping in a lev-1-dependent fashion. Interestingly, this response was independent of unc-38, an alpha subunit of the nicotinic receptor classically expressed with lev-1 at the body wall muscle. This implies an uncharacterized lev-1-containing receptor underpins this effect. Overall, our results reveal that body wall cholinergic transmission not only controls locomotion but simultaneously inhibits feeding behavior.
101466
Izquierdo, Patricia G.
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Calahorro, Fernando
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Thisainathan, Thibana
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Atkins, James H.
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Haszczyn, Johanna
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Lewis, Christian J.
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Tattersall, John E.h.
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Green, A. Christopher
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Holden-dye, Lindy
8032bf60-5db6-40cb-b71c-ddda9d212c8e
O'connor, Vincent
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1 January 2022
Izquierdo, Patricia G.
819a11cd-238c-4031-901f-5921a04a20ee
Calahorro, Fernando
dddfa373-d3cc-433f-8851-9ca37f2f3950
Thisainathan, Thibana
b14aed45-0ba1-4ee2-b375-f8c3c078b9a8
Atkins, James H.
49cd073d-a27b-4d9a-8cea-71c422f4c64b
Haszczyn, Johanna
f55b4da4-7290-44b1-8043-8e7560b31c02
Lewis, Christian J.
6a953646-70d2-4785-9f6d-ee6f90b16cd5
Tattersall, John E.h.
82b5784c-d040-4483-ae31-cce48fa3b6be
Green, A. Christopher
72d85b3c-b173-4e3c-b5fb-7b6d63425239
Holden-dye, Lindy
8032bf60-5db6-40cb-b71c-ddda9d212c8e
O'connor, Vincent
8021b06c-01a0-4925-9dde-a61c8fe278ca
Izquierdo, Patricia G., Calahorro, Fernando, Thisainathan, Thibana, Atkins, James H., Haszczyn, Johanna, Lewis, Christian J., Tattersall, John E.h., Green, A. Christopher, Holden-dye, Lindy and O'connor, Vincent
(2022)
Cholinergic signaling at the body wall neuromuscular junction distally inhibits feeding behavior in Caenorhabditis elegans.
Journal of Biological Chemistry, 298 (1), , [101466].
(doi:10.1016/j.jbc.2021.101466).
Abstract
Complex biological functions within organisms are frequently orchestrated by systemic communication between tissues. In the model organism Caenorhabditis elegans, the pharyngeal and body wall neuromuscular junctions are two discrete structures that control feeding and locomotion, respectively. Separate, the well-defined neuromuscular circuits control these distinct tissues. Nonetheless, the emergent behaviors, feeding and locomotion, are coordinated to guarantee the efficiency of food intake. Here, we show that pharmacological hyperactivation of cholinergic transmission at the body wall muscle reduces the rate of pumping behavior. This was evidenced by a systematic screening of the effect of the cholinesterase inhibitor aldicarb on the rate of pharyngeal pumping on food in mutant worms. The screening revealed that the key determinants of the inhibitory effect of aldicarb on pharyngeal pumping are located at the body wall neuromuscular junction. In fact, the selective stimulation of the body wall muscle receptors with the agonist levamisole inhibited pumping in a lev-1-dependent fashion. Interestingly, this response was independent of unc-38, an alpha subunit of the nicotinic receptor classically expressed with lev-1 at the body wall muscle. This implies an uncharacterized lev-1-containing receptor underpins this effect. Overall, our results reveal that body wall cholinergic transmission not only controls locomotion but simultaneously inhibits feeding behavior.
Text
2021.02.12.430967v1.full
- Accepted Manuscript
More information
Accepted/In Press date: 1 August 2021
e-pub ahead of print date: 3 December 2021
Published date: 1 January 2022
Additional Information:
Funding Information:
Acknowledgments—We thank Dr Jean-Louis Bessereau, Dr Denise Walker, Dr William Schafer, Dr Mark Alkema, and Dr Michael Francis for sharing strains; and Dr Antonio Miranda-Vizuete for sharing Punc-122::gfp marker plasmid. We thank Emeritus Professor Robert Walker and Dr Helena Rawsthorne-Manning for critical reading of the article and for detailed comments. Additional C. elegans strains were provided by the CGC, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). This work was funded by the University of Southampton (United Kingdom) and the Defence Science and Technology Laboratory, Porton Down, Wiltshire (United Kingdom). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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© 2021 THE AUTHORS. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology.
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Local EPrints ID: 455897
URI: http://eprints.soton.ac.uk/id/eprint/455897
ISSN: 0021-9258
PURE UUID: ba7eb1d3-65cf-4dc2-9a4b-c17abb986e2d
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Date deposited: 07 Apr 2022 16:51
Last modified: 17 Mar 2024 03:32
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Author:
Patricia G. Izquierdo
Author:
Thibana Thisainathan
Author:
James H. Atkins
Author:
Christian J. Lewis
Author:
John E.h. Tattersall
Author:
A. Christopher Green
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