Evidence map›Paper›PMID 39979341›Full record

ArticleNature communications2025

Calcium levels in ASER neurons determine behavioral valence by engaging distinct neuronal circuits in C. elegans.

Weikang Xue, Yuanhua Chen, Ziyi Lei, Yuanxia Wang, Jiaze Liu, Xin Wen, Fang Xu, Pu Chen, Zhengxing Wu, Youngnam N Jin and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Weikang Xue *Department of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Yuanhua Chen *Department of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China. yuanhuachen2022@gmail.com.
Ziyi LeiDepartment of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Yuanxia WangDepartment of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Jiaze LiuDepartment of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Xin WenCollege of Life Science, Henan Agricultural University, Zhengzhou, China.
Fang XuDepartment of Biomedical Engineering, Tissue Engineering and Organ Manufacturing (TEOM) Lab, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, China.
Pu ChenDepartment of Biomedical Engineering, Tissue Engineering and Organ Manufacturing (TEOM) Lab, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, China.ORCID http://orcid.org/0000-0002-6857-2211
Zhengxing WuKey Laboratory of Molecular Biophysics of Ministry of Education, Institute of Biophysics and Biochemistry, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0002-8336-5456
Youngnam N JinDepartment of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China. youngnam_jin@whu.edu.cn.ORCID http://orcid.org/0009-0007-2632-3237
Yanxun V YuDepartment of Neurology, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China. yanxunyu@whu.edu.cn.ORCID http://orcid.org/0000-0001-6617-0166

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2021ZD0202603National Natural Science Foundation of China (National Science Foundation of China) 32070832National Natural Science Foundation of China (National Science Foundation of China) 32150610476NIH HHS P40 OD010440
6 · The paper itself

Abstract

The valence of stimuli is shaped by various factors, including environmental cues, internal states, genetic variability, and past experience. However, the mechanisms behind this flexibility remain elusive. In the nematode C. elegans, we found that ethanol, an olfactory stimulus, can elicit opposite chemotaxis responses - attraction vs. aversion - depending on NaCl concentration, demonstrating the role of environmental factors in altering valence. Remarkably, a single chemosensory neuron, ASER, orchestrate this bidirectional ethanol chemotaxis by integrating information from both stimuli - ethanol and NaCl - into its neuronal activity dynamics. Specifically, different calcium dynamics in the ASER neuron differentially activate the signaling molecule CMK-1, thereby engaging different downstream interneurons and leading to opposite chemotaxis directions. Consistently, optogenetic manipulations of the ASER neuron reverse the chemotaxis directions, by altering its calcium dynamics. Our findings reveal a mechanism by which a single neuron integrates multisensory inputs to determine context-dependent behavioral valence, contributing to our current understanding of valence encoding.

Indexed as

Caenorhabditis elegansCalciumNeuronsAnimalsAnimals, Genetically ModifiedBehavior, AnimalCaenorhabditis elegans ProteinsChemotaxisEthanolInterneuronsOptogeneticsSodium ChlorideCaenorhabditis elegans ProteinsCalciumEthanolSodium Chloride

Identifiers

PMID39979341
PMCPMC11842750

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.