Evidence map›Paper›PMID 40012396›Full record

ReviewCurrent neuropharmacology2026

Roles of Microglia in Synaptogenesis, Synaptic Pruning, and Synaptic Plasticity in Physiological Conditions and Central Nervous System Disorders.

Meizhen Xie, Tian Wang, Jiachun Feng, Di Ma, Liangshu Feng, Yulei Hao

Abstract readReview
In one paragraph

Review in Current neuropharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Neuroimmune Mechanisms and Emerging Intervention Strategies for Post-Stroke Fatigue: A Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Bidirectional Interplay Between Microglia and Mast Cells.International journal of molecular sciences · 2025
    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

6 authors.

Meizhen XieCell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht 3584 CH, The Netherlands.
Tian WangThe Second Hospital of Jilin University, Changchun, Jilin Province 130021, People's Republic of China.
Jiachun FengDepartment of Neurology and Neuroscience Center, The First Hospital of Jilin University, Xinmin Street No. 1, Changchun, Jilin Province 130021, China.
Di MaDepartment of Neurology and Neuroscience Center, The First Hospital of Jilin University, Xinmin Street No. 1, Changchun, Jilin Province 130021, China.
Liangshu FengStroke Center, Department of Neurology, The First Hospital of Jilin University, Xinmin Street No. 1 , Changchun, Jilin Province 130021, China.
Yulei HaoDoctor of Excellence Program (DEP), The First Hospital of Jilin University, Xinmin Street No. 1, Changchun, Jilin Province 130021, China.

Funding

Young Scientists Fund of the National Nature Science Foundation of China 82301425
6 · The paper itself

Abstract

Microglia are resident immune cells in the brain that have been widely studied for their immune surveillance and phagocytosis. In recent years, the important role of microglia in synapse formation, elimination, and plasticity is gradually being recognized. Synapses are the main communication mode between neurons. They undergo constant changes in quantity and plasticity throughout the life cycle, which is the basis of learning and memory. Microglia are highly motile, branched forms that monitor the microenvironment of the central nervous system (CNS) and promote synapse formation and maturation. They recognize and phagocytose redundant synapses through specific phagocytosis receptors. Furthermore, microglia regulate synaptic plasticity by releasing various effectors. The roles of microglia on synapses ensure the proper function of neural networks. Synaptic dysfunction and microglia activation are common features in CNS disorders, such as Alzheimer's disease, Parkinson's disease, ischemic stroke, cerebral hemorrhage, traumatic brain injury, multiple sclerosis, and epilepsy. Highly heterogeneous microglia exhibit diverse functions in these diseases and participate in disease progression by exacerbating or inhibiting synaptic dysfunction, in addition to neuroimmune and inflammation. In this article, we summarize the role of microglia on synapses under physiological conditions and in CNS disorders. We highlight the possible mechanisms by which microglia regulate synapse function in CNS disorders and how this affects the progression of the diseases. We aim to explore potential therapeutic targets for CNS disorders.

Indexed as

Central Nervous System DiseasesMicrogliaNeurogenesisNeuronal PlasticitySynapsesAnimalsHumansAlzheimer’s diseaseischemic stroke.microgliaParkinson’s diseasesynapsesynaptic plasticitysynaptogenesistranscriptomic

Identifiers

PMID40012396
PMCPMC13054735

What OpenQuestion holds

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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.