Evidence map›Paper›PMID 38926390›Full record

ArticleNature communications2024

Microglia contribute to neuronal synchrony despite endogenous ATP-related phenotypic transformation in acute mouse brain slices.

Péter Berki, Csaba Cserép, Zsuzsanna Környei, Balázs Pósfai, Eszter Szabadits, Andor Domonkos, Anna Kellermayer, Miklós Nyerges, Xiaofei Wei, Istvan Mody and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Microglia Modulate Information Processing in the Mouse Barrel Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  4. Article
  5. Article
  6. Microglial activation and RAS signaling: a dual-edged sword in neuroinflammation.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Capturing the Electrical Activity of all Cortical Neurons: Are Solutions Within Reach?Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  12. Review
  13. Article
  14. Article
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

20 authors.

Péter Berki *János Szentágothai Doctoral School of Neuroscience, Semmelweis University, Budapest, H-1083, Hungary.
Csaba Cserép *Momentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0001-5513-2471
Zsuzsanna Környei *Momentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0001-8281-7994
Balázs PósfaiMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0003-1035-565X
Eszter SzabaditsMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.
Andor DomonkosMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0002-0007-5948
Anna KellermayerMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.
Miklós NyergesMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0001-5044-6439
Xiaofei WeiDepartment of Neurology, The David Geffen School of Medicine at UCLA, Los Angeles, CA, 90095, USA.ORCID 0000-0002-1173-4734
Istvan ModyDepartment of Neurology, The David Geffen School of Medicine at UCLA, Los Angeles, CA, 90095, USA.ORCID 0000-0002-7975-7959
Araki KunihikoInstitute of Experimental Epileptology and Cognition Research, Medical University of Bonn, Bonn, 53127, Germany.
Heinz BeckInstitute of Experimental Epileptology and Cognition Research, Medical University of Bonn, Bonn, 53127, Germany.
He KaikaiState Key Laboratory of Membrane Biology, New Cornerstone Science Laboratory, School of Life Sciences, Peking University, 100871, Beijing, China.
Wang YaChinese Institute for Brain Research, 102206, Beijing, China.
Nikolett LénártMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.
Zhaofa WuState Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, 100101, Beijing, China.ORCID 0000-0003-2027-5194
Miao JingChinese Institute for Brain Research, 102206, Beijing, China.ORCID 0000-0002-7782-5065
Yulong LiState Key Laboratory of Membrane Biology, New Cornerstone Science Laboratory, School of Life Sciences, Peking University, 100871, Beijing, China.ORCID 0000-0002-9166-9919
Attila I GulyásLaboratory of Cerebral Cortex Research, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary.ORCID 0000-0003-4961-636X
Ádám DénesMomentum Laboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, H-1083, Hungary. denes.adam@koki.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute brain slices represent a workhorse model for studying the central nervous system (CNS) from nanoscale events to complex circuits. While slice preparation inherently involves tissue damage, it is unclear how microglia, the main immune cells and damage sensors of the CNS react to this injury and shape neuronal activity ex vivo. To this end, we investigated microglial phenotypes and contribution to network organization and functioning in acute brain slices. We reveal time-dependent microglial phenotype changes influenced by complex extracellular ATP dynamics through P2Y12R and CX3CR1 signalling, which is sustained for hours in ex vivo mouse brain slices. Downregulation of P2Y12R and changes of microglia-neuron interactions occur in line with alterations in the number of excitatory and inhibitory synapses over time. Importantly, functional microglia modulate synapse sprouting, while microglial dysfunction results in markedly impaired ripple activity both ex vivo and in vivo. Collectively, our data suggest that microglia are modulators of complex neuronal networks with important roles to maintain neuronal network integrity and activity. We suggest that slice preparation can be used to model time-dependent changes of microglia-neuron interactions to reveal how microglia shape neuronal circuits in physiological and pathological conditions.

Indexed as

Adenosine TriphosphateBrainCX3C Chemokine Receptor 1MicrogliaNeuronsReceptors, Purinergic P2Y12SynapsesAnimalsMaleMiceMice, Inbred C57BLPhenotypeSignal TransductionAdenosine TriphosphateCX3C Chemokine Receptor 1Cx3cr1 protein, mouseP2ry12 protein, mouseReceptors, Purinergic P2Y12

Identifiers

PMID38926390
PMCPMC11208608

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.