Evidence map›Paper›PMID 40381194›Full record

ArticleCell reports2025

Optogenetic activation of cortical microglia promotes neuronal activity and pain hypersensitivity.

Min-Hee Yi, Yi Liu, Yong U Liu, Jinkyung Lee, Priyanka Hanumaihgari, Sebastian Parusel, Dale B Bosco, Lingxiao Wang, Jiaying Zheng, Wu Shi and 4 more

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. VlPAG/DRN Microglia Drive Neuropathic Pain-Induced Depression via a Defined Neuroimmune Axis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
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

14 authors.

Min-Hee YiDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Department of Microbiology and Immunology, Chonnam National University Medical School, Hwasun, Jeollanam-do 58128, Republic of Korea; Institute for Biomedical Science (IBS) of Chonnam National University Hwasun Hospital, Hwasun, Jeollanam-do 58128, Republic of Korea; BioMedical Sciences Graduate Program (BMSGP), Chonnam National University, Hwasun, Jeollanam-do 58128, Republic of Korea.
Yi LiuDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Center for Neuroimmunology and Glial Biology, Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA; Department of Anesthesiology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510080, China.
Yong U LiuDepartment of Anesthesiology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, China.
Jinkyung LeeBioMedical Sciences Graduate Program (BMSGP), Chonnam National University, Hwasun, Jeollanam-do 58128, Republic of Korea.
Priyanka HanumaihgariDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Department of Neuroscience, Johns Hopkins Medical Institute, Baltimore, MD 21205, USA.
Sebastian ParuselDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Dale B BoscoDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Lingxiao WangDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Jiaying ZhengDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Center for Neuroimmunology and Glial Biology, Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA.
Wu ShiDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Center for Neuroimmunology and Glial Biology, Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA.
Lattawat EauchaiDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Supin ChompoopongFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Christine L HuntDepartment of Pain Medicine, Mayo Clinic, Jacksonville, FL 32224, USA.
Long-Jun WuDepartment of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Center for Neuroimmunology and Glial Biology, Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA. Electronic address: longjun.wu@uth.tmc.edu.

Funding

The glial mechanism for electrical brain stimulationR01NS112144 · NINDS · MAYO CLINIC ROCHESTER · PI WANG, HAI-LONG, WORRELL, GREGORY A · 2019 to 2023
$3.8M
How microglia sense and regulate neuronal activity in the adult brainR35NS132326 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Long-Jun Wu · 2023 to 2026
$3.2M
Microglial regulation of neuronal activity in TDP-43 neurodegenerationRF1AG082314 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, LONG-JUN · 2023 to 2023
$1.9M
Optimizing Pharmacotherapy with Noninvasive Wearable Sensors and Subscalp EEGUH3NS123066 · NINDS · MAYO CLINIC ROCHESTER · PI Benjamin H Brinkmann, Gregory A Worrell · 2025 to 2026
$1.4M
Microglial regulation of neuronal activity in TDP-43 neurodegenerationR01AG082314 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Long-Jun Wu · 2026 to 2026
$712k
NIA NIH HHS R01 AG082314NIA NIH HHS RF1 AG082314NINDS NIH HHS R01 NS112144NINDS NIH HHS R35 NS132326NINDS NIH HHS UH3 NS123066
6 · The paper itself

Abstract

Chronic pain following peripheral nerve injury is accompanied by increased neuronal activity in the somatosensory cortex. However, whether and how cortical microglia contribute to these changes is less understood. To this end, we applied an optogenetic strategy to specifically target cortical microglia and investigate their function in behavioral pain sensitization. We found that optogenetic activation of microglia in the primary somatosensory cortex (S1) via red-activated channelrhodopsin (ReaChR) triggered pain hypersensitivity and affective-motivational responses in mice. Remarkably, S1-targeted optogenetic stimulation increased microglial landscape changes and ATP release. In addition, optogenetic stimulation altered the microglial proteomic profile, upregulated neuronal c-Fos expression, and enhanced neuronal Ca

Indexed as

HyperalgesiaMicrogliaNeuronsOptogeneticsSomatosensory CortexAdenosine TriphosphateAnimalsChannelrhodopsinsMaleMiceMice, Inbred C57BLProto-Oncogene Proteins c-fosAdenosine TriphosphateChannelrhodopsinsProto-Oncogene Proteins c-fosATPchronic painCP: Neurosciencemicrogliamicroglial landscape changeoptogeneticsReaChRsomatosensory cortextwo-photon imaging

Identifiers

PMID40381194
PMCPMC12161772

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.