Evidence map›Paper›PMID 41569490›Full record

ReviewAdvances in neurobiology2026

Roles of Glia in Synapse Nano-organization.

Young-Jin Choi, Won-Suk Chung

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Young-Jin ChoiCenter for Vascular Research, Institute for Basic Science, Daejeon, Republic of Korea.
Won-Suk ChungCenter for Vascular Research, Institute for Basic Science, Daejeon, Republic of Korea. wonsuk.chung@kaist.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glia, which are nonneuronal cells in the central nervous system, include astrocytes, microglia, and oligodendrocyte lineage cells. Historically, their passive roles in maintaining central nervous system function-such as supplying substrates for neuronal energy, buffering neurotransmitters, and improving neural conductance-have been primarily highlighted. Importantly, recent research has revealed that glial cells express genes directly related to controlling synapse nano-organization. In particular, astrocytes have the ability to secrete molecules that induce synapse formation and maturation. They also modulate the structure of synapses by expressing proteins that make direct contact with the synaptic membrane. Moreover, astrocytes can actively eliminate synapses through their phagocytic machinery during development and adulthood, thereby establishing circuit homeostasis. Microglia can also assist in the integration of synapses into the neural circuit and regulate synapse formation, maintenance, and elimination. Here, we review key findings on the mechanisms of glial contributions to synapse nano-organization. We will also discuss how different glial cells contribute to the development and homeostasis of synapses through distinct cellular and molecular pathways in both health and disease.

Indexed as

AstrocytesMicrogliaNeurogliaOligodendrogliaSynapsesAnimalsHumansNeurodevelopmentAstrocytesMicrogliaOligodendrocyte precursor cellsSynapse eliminationSynapse formationSynapse nano-organization

Identifiers

What Socratic holds

Textmetadata
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.