Evidence map›Paper›PMID 39548079›Full record

ArticleNature communications2024

Membrane lipid nanodomains modulate HCN pacemaker channels in nociceptor DRG neurons.

Lucas J Handlin, Natalie L Macchi, Nicolas L A Dumaire, Lyuba Salih, Erin N Lessie, Kyle S McCommis, Aubin Moutal, Gucan Dai

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Lucas J HandlinEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, USA.ORCID 0009-0008-0960-742X
Natalie L MacchiEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, USA.
Nicolas L A DumaireDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, Saint Louis, USA.ORCID 0000-0001-9905-1366
Lyuba SalihDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, Saint Louis, USA.
Erin N LessieEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, USA.
Kyle S McCommisEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, USA.ORCID 0000-0003-2381-1589
Aubin MoutalDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, Saint Louis, USA.ORCID 0000-0003-4268-1206
Gucan DaiEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, USA. gucan.dai@health.slu.edu.ORCID 0000-0002-4692-4060

Funding

Exploring CRMP5 as a novel target for Alzheimers diseaseR01NS119263 · NINDS · UNIVERSITY OF ARIZONA · PI Aubin Moutal · 2021 to 2026
$2.2M
VOLTAGE-SENSING MECHANISMS OF ION CHANNELS IN DYNAMIC LIPID MEMBRANESR35GM154778 · NIGMS · SAINT LOUIS UNIVERSITY · PI Gucan Dai · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM154778NINDS NIH HHS R01 NS119263U.S. Department of Defense (United States Department of Defense) CP220080P1U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM154778U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS119263U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS119263-04S1
6 · The paper itself

Abstract

Cell membranes consist of heterogeneous lipid nanodomains that influence key cellular processes. Using FRET-based fluorescent assays and fluorescence lifetime imaging microscopy (FLIM), we find that the dimension of cholesterol-enriched ordered membrane domains (OMD) varies considerably, depending on specific cell types. Particularly, nociceptor dorsal root ganglion (DRG) neurons exhibit large OMDs. Disruption of OMDs potentiated action potential firing in nociceptor DRG neurons and facilitated the opening of native hyperpolarization-activated cyclic nucleotide-gated (HCN) pacemaker channels. This increased neuronal firing is partially due to an increased open probability and altered gating kinetics of HCN channels. The gating effect on HCN channels is likely due to a direct modulation of their voltage sensors by OMDs. In animal models of neuropathic pain, we observe reduced OMD size and a loss of HCN channel localization within OMDs. Additionally, cholesterol supplementation inhibited HCN channels and reduced neuronal hyperexcitability in pain models. These findings suggest that disturbances in lipid nanodomains play a critical role in regulating HCN channels within nociceptor DRG neurons, influencing pain modulation.

Indexed as

CholesterolGanglia, SpinalHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsNociceptorsAction PotentialsAnimalsHumansMaleMembrane LipidsMembrane MicrodomainsMiceMice, Inbred C57BLNeuralgiaRatsCholesterolHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsMembrane Lipids

Identifiers

PMID39548079
PMCPMC11568329

What OpenQuestion holds

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Registered trials

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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.