Evidence map›Paper›PMID 36289499›Full record

ArticleMolecular brain2022

Spinal microglia contribute to sustained inflammatory pain via amplifying neuronal activity.

Nan Gu, Min-Hee Yi, Madhuvika Murugan, Manling Xie, Sebastian Parusel, Jiyun Peng, Ukpong B Eyo, Christine L Hunt, Hailong Dong, Long-Jun Wu

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 23 citations in OpenAlex.

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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

10 authors at 4 institutions in 2 countries.

Nan Gu *Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Min-Hee Yi *Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
Madhuvika MuruganDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Manling XieDepartment of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
Sebastian ParuselDepartment of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
Jiyun PengDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Ukpong B EyoDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Christine L HuntDepartment of Pain Medicine, Mayo Clinic, Jacksonville, FL, 32224, USA.
Hailong DongDepartment of Anesthesiology & Perioperative Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, 710032, PR China. hldong6@hotmail.com.
Long-Jun WuDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA. wu.longjun@mayo.edu.ORCID 0000-0001-8019-3380
Rutgers, The State University of New Jersey · USMayo Clinic · USMayo Clinic in Florida · USXijing Hospital · CN

Funding

The glial mechanism for electrical brain stimulationR01NS112144 · NINDS · MAYO CLINIC ROCHESTER · PI WANG, HAI-LONG, WORRELL, GREGORY A · 2019 to 2023
$3.8M
The Role of Microglia in EpilepsyR01NS088627 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, LONG-JUN · 2014 to 2023
$3.6M
The role of microglia in neuromyelitis opticaR01NS110949 · NINDS · MAYO CLINIC ROCHESTER · PI LENNON, VANDA A, WU, LONG-JUN · 2020 to 2024
$2.0M
NINDS NIH HHS R01 NS088627NINDS NIH HHS R01NS088627NINDS NIH HHS R01 NS110949NINDS NIH HHS R01NS110949NINDS NIH HHS R01 NS112144
6 · The paper itself

Abstract

Microglia are highly dynamic immune cells of the central nervous system (CNS). Microglial processes interact with neuronal elements constantly on the order of minutes. The functional significance of this acute microglia-neuron interaction and its potential role in the context of pain is still largely unknown. Here, we found that spinal microglia increased their process motility and electrophysiological reactivity within an hour after the insult in a mouse model of formalin-induced acute, sustained, inflammatory pain. Using an ablation strategy to specifically deplete resident microglia in the CNS, we demonstrate that microglia participate in formalin-induced acute sustained pain behaviors by amplifying neuronal activity in the spinal dorsal horn. Moreover, we identified that the P2Y12 receptor, which is specifically expressed in microglia in the CNS, was required for microglial function in formalin-induced pain. Taken together, our study provides a novel insight into the contribution of microglia and the P2Y12 receptor in inflammatory pain that could be used for potential therapeutic strategies.

Indexed as

MicrogliaNeuralgiaAnimalsFormaldehydeMiceNeuronsPurinergic P2Y Receptor AntagonistsFormaldehydePurinergic P2Y Receptor AntagonistsFormalinInflammatory painMicrogliaMicroglia–neuron interactionP2Y12 receptorTwo-photon imaging

Identifiers

PMID36289499
PMCPMC9609165
OpenAlexW4307659024

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.