Evidence map›Paper›PMID 35394085›Full record

ArticleGlia2022

Microglia maintain the normal structure and function of the hippocampal astrocyte network.

Yixing Du, Faith H Brennan, Phillip G Popovich, Min Zhou

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  5. Glial Cells in Behavioral and Psychological Symptoms of Alzheimer's Disease.International journal of molecular sciences · 2026
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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

4 authors at 1 institution in 1 country.

Yixing DuDepartment of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.ORCID 0000-0001-7728-7095
Faith H BrennanDepartment of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.ORCID 0000-0002-9201-2476
Phillip G PopovichDepartment of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.ORCID 0000-0003-1329-7395
Min ZhouDepartment of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.ORCID 0000-0001-6249-2977
The Ohio State University Wexner Medical Center · US

Funding

Overcoming Neurogenic “Meta-Inflammation” to Promote Recovery After Spinal Cord InjuryR35NS111582 · NINDS · OHIO STATE UNIVERSITY · PI PHILLIP G POPOVICH · 2019 to 2026
$8.7M
Preventing autonomic dysreflexia to restore immune function after SCIR01NS083942 · NINDS · OHIO STATE UNIVERSITY · PI POPOVICH, PHILLIP G · 2014 to 2018
$2.2M
Functional plasticity of astrocyte syncytial networkR01NS116059 · NINDS · OHIO STATE UNIVERSITY · PI ZHOU, MIN · 2020 to 2024
$1.9M
Role of the spinal cord - gut - immune axis after spinal cord injuryR01NS099532 · NINDS · OHIO STATE UNIVERSITY · PI POPOVICH, PHILLIP G · 2017 to 2018
$1.0M
NINDS NIH HHS R01 NS083942NINDS NIH HHS R01 NS099532NINDS NIH HHS R01 NS116059NINDS NIH HHS R35 NS111582
6 · The paper itself

Abstract

Microglial control of activity-dependent plasticity and synaptic remodeling in neuronal networks has been the subject of intense research in the past several years. Although microglia-neuron interactions have been extensively studied, less is known about how microglia influence astrocyte-dependent control over neuronal structure and function. Here, we explored a role for microglia in regulating the structure and function of the astrocyte syncytium in mouse hippocampus. After depleting microglia using a CSF1R antagonist (PLX5622, Plexxikon), we observed severe disruption of astrocyte syncytial isopotentiality and dye coupling. A decrease in astrocyte-specific gap junction connexin (Cx) 30 and 43 expression, at least partially accounts for these microglia-dependent changes in astrocytes. Because neuronal function requires intact astrocyte coupling, we also evaluated the effects of microglia depletion on synaptic transmission in the hippocampus. Without microglia, the strength of synaptic transmission was reduced at baseline and after long-term potentiation (LTP). Conversely, priming microglia with systemic injections of lipopolysaccharide enhanced CA3-CA1 synaptic transmission. This microglia-induced scaling of synaptic transmission was associated with increased expression of post-synaptic scaffold proteins (Homer1) in CA1. However, astrocyte network function was not affected by microglia priming, indicating that microglia-dependent effects on astrocytes and neurons vary across functional states. Through manipulation of microglia in the brain, our results reveal the importance of microglia in homeostatic regulation of the astrocyte syncytium and scaling of synaptic transmission. These novel mechanisms uncover a new direction for future studies interrogating microglia function in various physiological and pathological contexts.

Indexed as

AstrocytesMicrogliaAnimalsConnexin 30HippocampusLong-Term PotentiationMiceNeuronal PlasticitySynaptic TransmissionConnexin 30astrocyteshippocampusmicrogliasynaptic plasticitysynaptic transmission

Identifiers

PMID35394085
PMCPMC9324808
OpenAlexW4224283842

What Socratic 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 Socratic graph.