Evidence map›Paper›PMID 36701202›Full record

ArticleThe Journal of clinical investigation2023

A TRPV4-dependent neuroimmune axis in the spinal cord promotes neuropathic pain.

Xueming Hu, Lixia Du, Shenbin Liu, Zhou Lan, Kaikai Zang, Jing Feng, Yonghui Zhao, Xingliang Yang, Zili Xie, Peter L Wang and 8 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

63 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  4. Glial cells in neuropathic pain.Physiological reviews · 2026
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3 more citing papers are in PubMed but not listed here.

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

18 authors at 4 institutions in 3 countries.

Xueming HuDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Lixia DuDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Shenbin LiuDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Zhou LanDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Kaikai ZangDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Jing FengDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Yonghui ZhaoDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Xingliang YangDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Zili XieDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Peter L WangDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Aaron M Ver HeulDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Lvyi ChenDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Vijay K SamineniDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Yan-Qing WangInstitute of Acupuncture and Moxibustion and Institute of Integrative Medicine; Department of Integrative Medicine and Neurobiology, School of Basic Medical Science; and State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, Fudan University, Shanghai, China.
Kory J LavineDepartment of Internal Medicine, Cardiovascular Division and.
Robert W GereauDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Gregory F WuDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Hongzhen HuDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, and Washington University Pain Center and.
Washington Center · USWashington University in St. Louis · USCardiovascular Research Center · BRShanghai Medical College of Fudan University · CN

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Training Grant in Molecular Imaging Research (MGH/HMS)T32CA079443 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2025
$10.1M
Specification and Function of Tissue Resident and Recruited Macrophages in Cardiac Remodeling and Heart FailureR35HL161185 · NHLBI · WASHINGTON UNIVERSITY · PI Kory J. Lavine · 2022 to 2026
$4.3M
TARGETING THE TRANSIENT RECEPTOR POTENTIAL CHANNELS TO IMPROVE BOWEL DYSFUNCTIONR01DK103901 · NIDDK · WASHINGTON UNIVERSITY · PI HU, HONGZHEN · 2015 to 2023
$3.4M
Deciphering the Piezo2-Merkel cell signaling mechanisms in itchR01AR077183 · NIAMS · WASHINGTON UNIVERSITY · PI HU, HONGZHEN · 2020 to 2024
$2.6M
MECHANISMS OF TRPV4-MEDIATED NEUROPATHIC PAINR01AA027065 · NIAAA · WASHINGTON UNIVERSITY · PI HU, HONGZHEN · 2018 to 2022
$2.5M
Neural Mechanisms Underlying IC/BPSR01DK128475 · NIDDK · WASHINGTON UNIVERSITY · PI SAMINENI, VIJAY K · 2021 to 2025
$2.3M
The Role of TRPV4 in central nervous system immunity and diseaseR01NS106289 · NINDS · WASHINGTON UNIVERSITY · PI WU, GREGORY · 2018 to 2021
$1.6M
DEFINING THE NEURAL BASIS FOR CHRONIC BLADDER PAIN AND ITS ASSOCIATED COMORBID DISORDERSK01DK115634 · NIDDK · WASHINGTON UNIVERSITY · PI SAMINENI, VIJAY K · 2018 to 2022
$582k
Skin Neuroimmune Mechanisms of Urticarial ItchK08AR080219 · NIAMS · WASHINGTON UNIVERSITY · PI VER HEUL, AARON · 2022 to 2024
$438k
NCI NIH HHS T32 CA079443NHLBI NIH HHS R35 HL161185NIAAA NIH HHS R01 AA027065NIAMS NIH HHS K08 AR080219NIAMS NIH HHS R01 AR077183NIDDK NIH HHS K01 DK115634NIDDK NIH HHS P30 DK052574NIDDK NIH HHS R01 DK103901NIDDK NIH HHS R01 DK128475NINDS NIH HHS R01 NS106289
6 · The paper itself

Abstract

Microglia, resident macrophages of the CNS, are essential to brain development, homeostasis, and disease. Microglial activation and proliferation are hallmarks of many CNS diseases, including neuropathic pain. However, molecular mechanisms that govern the spinal neuroimmune axis in the setting of neuropathic pain remain incompletely understood. Here, we show that genetic ablation or pharmacological blockade of transient receptor potential vanilloid type 4 (TRPV4) markedly attenuated neuropathic pain-like behaviors in a mouse model of spared nerve injury. Mechanistically, microglia-expressed TRPV4 mediated microglial activation and proliferation and promoted functional and structural plasticity of excitatory spinal neurons through release of lipocalin-2. Our results suggest that microglial TRPV4 channels reside at the center of the neuroimmune axis in the spinal cord, which transforms peripheral nerve injury into central sensitization and neuropathic pain, thereby identifying TRPV4 as a potential new target for the treatment of chronic pain.

Indexed as

NeuralgiaNeuroimmunomodulationAnimalsMiceMicrogliaSpinal CordTRPV Cation ChannelsTrpv4 protein, mouseTRPV Cation ChannelsNeurosciencePain

Identifiers

PMID36701202
PMCPMC9974096
OpenAlexW4318071678

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.