Evidence map›Paper›PMID 40646506›Full record

ReviewJournal of translational medicine2025

TREM2-mediated regulation of microglial activity: a promising target for the treatment of ischemic stroke.

Haihan Yu, Li Zhang, Bo Song, Kaidi Ren, Xing Chen, Yuwan Dai, Yang Yang, Yuming Xu, Ziqing Wei

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Designing Neural Dynamics: From Digital Twin Modeling to Regeneration.International journal of molecular sciences · 2025
    Review
  12. 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

9 authors.

Haihan Yu *Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China.
Li Zhang *Key Clinical Laboratory of Henan Province, Department of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China.
Bo SongDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China.
Kaidi RenDepartment of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China.
Xing ChenClinical Systems Biology Laboratories, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China.
Yuwan DaiDepartment of Blood Transfusion, Henan Provincial People's Hospital, Zhengzhou, 450003, P. R. China.
Yang YangClinical Systems Biology Laboratories, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China. yangyangbio@163.com.
Yuming XuDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China. 13903711125@126.com.
Ziqing WeiDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, P. R. China. ziqingwei102@163.com.ORCID 0009-0007-7314-0265

Funding

National Natural Science Foundation of China 82201455National Natural Science Foundation of China 82204389National Natural Science Foundation of China 82301342National Natural Science Foundation of China 82470403
6 · The paper itself

Abstract

Ischemic stroke, the most prevalent type of stroke globally, poses significant challenges due to its high incidence, morbidity, and long-term disability. Microglia, the resident immune cells of the central nervous system (CNS), play a dual role in the context of ischemic stroke. While they contribute to neuroinflammation by releasing pro-inflammatory cytokines and exacerbating neuronal injury, they also facilitate tissue repair, angiogenesis, and restoration of the blood-brain barrier (BBB) integrity through the secretion of anti-inflammatory and neurotrophic factors. Triggering receptor expressed on myeloid cells 2 (TREM2), predominantly expressed on microglia, is a critical regulator of microglial proliferation, survival, phagocytosis, polarization, inflammation, and metabolism. TREM2 has emerged as a key modulator of immune responses in ischemic stroke. This review provides a comprehensive examination of the multifaceted roles of TREM2 in microglial biology during ischemic stroke, integrating current insights into its molecular mechanisms. Furthermore, it highlights TREM2's potential as a transformative therapeutic target, advancing our understanding of neuroimmune regulation and promoting recovery after stroke.

Indexed as

Ischemic StrokeMembrane GlycoproteinsMicrogliaMolecular Targeted TherapyReceptors, ImmunologicAnimalsHumansMembrane GlycoproteinsReceptors, ImmunologicTREM2 protein, humanIschemic strokeMicrogliaNeuroinflammationTherapeutic targetTriggering receptor expressed on myeloid cells 2 (TREM2)

Identifiers

PMID40646506
PMCPMC12247297

What Socratic 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 Socratic graph.