Evidence map›Paper›PMID 38421867›Full record

ArticleCell reports2024

Neuron cilia restrain glial KCC-3 to a microdomain to regulate multisensory processing.

Sneha Ray, Pralaksha Gurung, R Sean Manning, Alexandra A Kravchuk, Aakanksha Singhvi

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

14 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  7. Review
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  10. Dendrite glia interactions: lessons from theFrontiers in cell and developmental biology · 2025
    Review
  11. Glia Development and Function in the NematodeCold Spring Harbor perspectives in biology · 2024
    Review
  12. Article
  13. Review
  14. Article
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

5 authors at 2 institutions in 1 country.

Sneha RayDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA; Neuroscience Graduate Program, University of Washington, Seattle, WA 98195, USA.
Pralaksha GurungDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA; Neuroscience Graduate Program, University of Washington, Seattle, WA 98195, USA.
R Sean ManningDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Alexandra A KravchukDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA; Department of Biology, University of Washington, Seattle, WA 98195, USA.
Aakanksha SinghviDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA; Department of Biological Structure, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address: asinghvi@fredhutch.org.
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Molecular dissection of glia-neuron interactionsR01NS114222 · NINDS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SINGHVI, AAKANKSHA · 2020 to 2024
$2.2M
Reimbursement request for attending the Meeting of the Jointly Sponsored Institutional Predoctoral Training in the Neurosciences T32 Program Directors in Baltimore, MD on 2/19/19T32NS099578 · NINDS · UNIVERSITY OF WASHINGTON · PI SULLIVAN, JANE M, WONG, RACHEL O · 2016 to 2020
$1.4M
NCI NIH HHS P30 CA015704NIH HHS P40 OD010440NINDS NIH HHS R01 NS114222NINDS NIH HHS T32 NS099578
6 · The paper itself

Abstract

Glia interact with multiple neurons, but it is unclear whether their interactions with each neuron are different. Our interrogation at single-cell resolution reveals that a single glial cell exhibits specificity in its interactions with different contacting neurons. Briefly, C. elegans amphid sheath (AMsh) glia apical-like domains contact 12 neuron-endings. At these ad-neuronal membranes, AMsh glia localize the K/Cl transporter KCC-3 to a microdomain exclusively around the thermosensory AFD neuron to regulate its properties. Glial KCC-3 is transported to ad-neuronal regions, where distal cilia of non-AFD glia-associated chemosensory neurons constrain it to a microdomain at AFD-contacting glial membranes. Aberrant KCC-3 localization impacts both thermosensory (AFD) and chemosensory (non-AFD) neuron properties. Thus, neurons can interact non-synaptically through a shared glial cell by regulating microdomain localization of its cues. As AMsh and glia across species compartmentalize multiple cues like KCC-3, we posit that this may be a broadly conserved glial mechanism that modulates information processing across multimodal circuits.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsCiliaNeurogliaNeuronsCaenorhabditis elegans ProteinsAFDC. eleganscell polarityciliaCP: Neurosciencegliaglial microdomainKCC-3neuron-glia signalingsensory processing

Identifiers

PMID38421867
PMCPMC11296322
OpenAlexW4392215281

What OpenQuestion 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 OpenQuestion graph.