OSCR

Ether phospholipids modulate somatosensory responses by tuning multiple receptor functions in <i>Drosophila</i>.

Overview

Authors: Takuto Suito1,2, Xiangmei Deng1,2, Shoma Sato1,2, Kohjiro Nagao3, Christian Ganser2, Takayuki Uchihashi2,4, Motosuke Tsutsumi2,5, Tomomi Nemoto2,5,6, Yuji Hara7, Makoto Tominaga8, Takaaki Sokabe1,2,6
ORCID iDs: Kohjiro Nagao
  1. Section of Sensory Physiology, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Japan
  2. Exploratory Research Center on Life and Living Systems, National Institutes of Natural Sciences, Okazaki, Japan
  3. Department of Biophysical Chemistry, Kyoto Pharmaceutical University, Kyoto, Japan
  4. Department of Physics, Nagoya University, Nagoya, Japan
  5. Division of Biophotonics, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Japan
  6. Graduate Institute for Advanced Studies, SOKENDAI, Hayama, Japan
  7. School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan
  8. Nagoya Advanced Research and Development Center, Nagoya City University, Nagoya, Japan
Journal: iScience, volume 29, issue 4, article 115209
Dates: received 29 August 2025; accepted 26 February 2026; published online 3 March 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1016/j.isci.2026.115209 · PMID 41907445 · PMCID PMC13018890 · OpenAlex W7133359689
Open access: gold, a free copy (OpenAlex)
Status: code on request
Categories: drosophila (organism), cellular / molecular (subfield)
Methods: Statistics, Evoked potentials, Single-unit activity, calcium imaging
Keywords: Mechanobiology, cell biology, model organism
Topic: Neurobiology and Insect Physiology Research (Cellular and Molecular Neuroscience, Neuroscience), according to OpenAlex
Funding: Japan Agency for Medical Research and Development (23gm6510014h0002); Japan Society for the Promotion of Science (21K15192, 19K23790, 21H02531, JP22H04926); RIKEN; Shizuoka University; Ministry of Education, Culture, Sports, Science and Technology
Citations: not cited yet (Europe PMC); 91 references in the paper
Research resources: α-GFP primary antibody RRID:AB_221570, α-Rabbit IgG-Alexa488 RRID:AB_2576217, α-Mouse-CD8a antibody RRID:AB_312751, pU6-BbsI-chiRNA vector RRID:Addgene_45946, Drosophila S2R+ RRID:CVCL_Z831, pHD-ScarlessDsRed vector RRID:DGRC_1364

Abstract

PIEZO and TRP channels are receptors for physical stimuli such as mechanical touch and temperature in sensory neurons. As these receptors are localized in the plasma membrane, the modulation of their activities by membrane lipids has recently attracted attention. In this study, we focused on ether phospholipids (ePLs) enriched in neurons and analyzed their role in somatosensation using Drosophila. Reduced mechanosensory behavior was observed with ePL-synthesizing gene knockout or knockdown in PIEZO-expressing neurons. PIEZO activation was significantly augmented in the presence of ePLs. Furthermore, we observed that ePLs modulate the thermosensory behavior and reduce the temperature threshold of TRPA1. Finally, we revealed that ePLs affect membrane tension and lipid order of the plasma membrane in cultured cells. Our study identified ePLs as a modulator of a specific set of receptors for multiple somatosensory modalities, which underscores the significance of functional interaction between membrane lipids and sensory channel proteins.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.

The paper's code and data availability statement is in the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none (its code is available on request), so it has no map.

Data

No dataset and no data link were found in the paper.

Data and code availability

All data reported in this article will be shared by the lead contact upon request.

This article does not report the original code.

Any additional information required to reanalyze the data reported in this article is available from the lead contact upon request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 30 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 11 authors, 3 keywords, 5 funders, 91 references, 6 RRIDs.

Cite

This paper

Suito, T., Deng, X., Sato, S., Nagao, K., Ganser, C., Uchihashi, T., Tsutsumi, M., Nemoto, T., Hara, Y., Tominaga, M., & Sokabe, T. (2026). Ether phospholipids modulate somatosensory responses by tuning multiple receptor functions in <i>Drosophila</i>. iScience, 29(4), 115209. https://doi.org/10.1016/j.isci.2026.115209

BibTeX

@article{suito2026ether,
author = {Suito, Takuto and Deng, Xiangmei and Sato, Shoma and Nagao, Kohjiro and Ganser, Christian and Uchihashi, Takayuki and Tsutsumi, Motosuke and Nemoto, Tomomi and Hara, Yuji and Tominaga, Makoto and Sokabe, Takaaki},
title = {{Ether phospholipids modulate somatosensory responses by tuning multiple receptor functions in \<i\>Drosophila\</i\>}},
journal = {iScience},
year = {2026},
month = mar,
volume = {29},
number = {4},
pages = {115209},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/j.isci.2026.115209},
url = {https://doi.org/10.1016/j.isci.2026.115209},
pmid = {41907445},
pmcid = {PMC13018890}
}

RIS

TY - JOUR
AU - Suito, Takuto
AU - Deng, Xiangmei
AU - Sato, Shoma
AU - Nagao, Kohjiro
AU - Ganser, Christian
AU - Uchihashi, Takayuki
AU - Tsutsumi, Motosuke
AU - Nemoto, Tomomi
AU - Hara, Yuji
AU - Tominaga, Makoto
AU - Sokabe, Takaaki
TI - Ether phospholipids modulate somatosensory responses by tuning multiple receptor functions in <i>Drosophila</i>
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/03/03
VL - 29
IS - 4
SP - 115209
SN - 2589-0042
PB - Elsevier
DO - 10.1016/j.isci.2026.115209
UR - https://doi.org/10.1016/j.isci.2026.115209
LA - en
ER -

CSL-JSON

{
"id": "10.1016/j.isci.2026.115209",
"type": "article-journal",
"title": "Ether phospholipids modulate somatosensory responses by tuning multiple receptor functions in <i>Drosophila</i>",
"container-title": "iScience",
"author": [
{
"family": "Suito",
"given": "Takuto"
},
{
"family": "Deng",
"given": "Xiangmei"
},
{
"family": "Sato",
"given": "Shoma"
},
{
"family": "Nagao",
"given": "Kohjiro"
},
{
"family": "Ganser",
"given": "Christian"
},
{
"family": "Uchihashi",
"given": "Takayuki"
},
{
"family": "Tsutsumi",
"given": "Motosuke"
},
{
"family": "Nemoto",
"given": "Tomomi"
},
{
"family": "Hara",
"given": "Yuji"
},
{
"family": "Tominaga",
"given": "Makoto"
},
{
"family": "Sokabe",
"given": "Takaaki"
}
],
"container-title-short": "iScience",
"volume": "29",
"issue": "4",
"page": "115209",
"DOI": "10.1016/j.isci.2026.115209",
"PMID": "41907445",
"PMCID": "PMC13018890",
"ISSN": "2589-0042",
"publisher": "Elsevier",
"URL": "https://doi.org/10.1016/j.isci.2026.115209",
"language": "en",
"issued": {
"date-parts": [
[
2026,
3,
3
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1038/s41467-026-76927-0 [code]
State-dependent binding of the wedge domain controls inactivation of the mechanosensitive ion channel PIEZO1.
Journal: Nature communications
In common: cellular / molecular, 5 references
[2] doi:10.1038/s41586-026-10182-7 [code]
The molecular basis of force selectivity by PIEZO2.
Journal: Nature
In common: cellular / molecular, 5 references
[3] doi:10.7554/elife.107867 [code]
Peripheral anatomy and central connectivity of proprioceptive sensory neurons in the <i>Drosophila</i> wing.
Journal: eLife
In common: drosophila, cellular / molecular, 2 references
[4] doi:10.7554/elife.105710 [code]
Neuropeptidergic circuit modulation of developmental sleep in <i>Drosophila</i>.
Journal: eLife
In common: drosophila, 2 references
[5] doi:10.1126/sciadv.aeh9771 [code]
Lipidomic profiling reveals age-dependent changes in plasma membrane lipids that affect neural stem cell aging.
Journal: Science advances
In common: 2 references
[6] doi:10.1038/s41467-026-76812-w [code]
Assessing molecular, cellular and transcriptomic bases of laminar perfusion and cytoarchitecture coupling in the human cortex.
Journal: Nature communications
In common: cellular / molecular, 2 references
[7] doi:10.1016/j.cdnut.2026.109508
Maternal Diet Enrichment in <i>n</i>-3 Long-Chain Polyunsaturated Fatty Acids during Pregnancy and Lactation Improves Their Transfer from the Mother to the Offspring and Counterbalances High-Fat Diet-Induced Alterations in a Sex-Dependent Manner in Rats.
Journal: Current developments in nutrition
In common: 2 references
[8] doi:10.1002/advs.202510538 [code]
Temporal and Cell-Specific Regulation of Synaptic Homeostasis by the Chromatin Remodeler Chd1.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
In common: drosophila, cellular / molecular, 1 reference
[9] doi:10.1038/s42255-026-01508-w
Neuronal lipid droplets play a conserved and sex-biased role in maintaining whole-body energy homeostasis.
Journal: Nature metabolism
In common: cellular / molecular, 2 references
[10] doi:10.1126/sciadv.aec4153
An octopamine-glutamate cotransmitting neuron gates aggressive escalation through layered inhibition in <i>Drosophila</i>.
Journal: Science advances
In common: drosophila, cellular / molecular, 1 reference

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.