Evidence map›Paper›PMID 33835613›Full record

ReviewThe European journal of neuroscience2021

An overview of microglia ontogeny and maturation in the homeostatic and pathological brain.

Monique S Mendes, Ania K Majewska

Open access · greenAbstract readReview
In one paragraph

Review in The European journal of neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

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  11. The Influence of Kynurenine Metabolites on Neurodegenerative Pathologies.International journal of molecular sciences · 2024
    Review
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  20. Synapse-specific plasticity relies on neuroimmune interactions.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

2 authors at 1 institution in 1 country.

Monique S MendesDepartment of Neuroscience, University of Rochester Medical Center, Rochester, NY, USA.ORCID 0000-0001-9800-5923
Ania K MajewskaDepartment of Neuroscience, University of Rochester Medical Center, Rochester, NY, USA.ORCID 0000-0002-2167-6849
University of Rochester Medical Center · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI B Paige Lawrence · 1985 to 2026
$42.8M
Dynamic neuroimmune interactions in the onset and progression of FASDR01AA027111 · NIAAA · UNIV OF ARKANSAS FOR MED SCIS · PI DREW, PAUL D, MAJEWSKA, ANNA K · 2018 to 2022
$2.3M
Mechanisms that regulate microglial dynamics in the context of plasticity (Supplement)R01NS114480 · NINDS · UNIVERSITY OF ROCHESTER · PI MAJEWSKA, ANNA K · 2020 to 2024
$2.2M
The effects of arousal on microglial motilityR21NS099973 · NINDS · UNIVERSITY OF ROCHESTER · PI MAJEWSKA, ANNA K · 2016 to 2017
$423k
The Role of Purinergic Signaling in Microglia Birth and Maturation in the Adult BrainK00NS108486 · NINDS · STANFORD UNIVERSITY · PI MENDES, MONIQUE SHANICE · 2021 to 2023
$232k
The role of purinergic signaling in mediating the dynamics of microglia repopulation following depletion in the adult cortex in vivoF99NS108486 · NINDS · UNIVERSITY OF ROCHESTER · PI MENDES, MONIQUE SHANICE · 2018 to 2020
$100k
NIAAA NIH HHS R01 AA027111NIEHS NIH HHS P30 ES001247NINDS NIH HHS F99 NS108486NINDS NIH HHS K00 NS108486NINDS NIH HHS R01 NS114480NINDS NIH HHS R21 NS099973
6 · The paper itself

Abstract

Microglia are the resident immune cells of the central nervous system (CNS) and are increasingly recognized as critical players in development, brain homeostasis, and disease pathogenesis. The lifespan, maintenance, proliferation, and turnover of microglia are important factors that regulate microglial behavior and affect their roles in the CNS. However, emerging evidence suggests that microglia are morphologically and phenotypically distinct in different brain areas, at different ages, and during disease. Ongoing research focuses on understanding how microglia acquire specific phenotypes in response to extrinsic cues in the environment and how phenotypes are specified by intrinsic properties of different populations of microglia. With the development of pharmacological and genetic tools that allow the investigation of microglia in vivo, there have been considerable advances in understanding molecular signatures of both homeostatic microglia and those reacting to injury and disease. Here, we review the master gene regulators that define microglia as well as discuss the evidence that microglia are heterogeneous and fall into distinct clusters that display specific intrinsic properties and perform unique tasks in different settings. Taken together, the information presented supports the idea that microglia morphology and transcriptional heterogeneity should be considered when studying the complex nature of microglia and their roles in brain health and disease.

Indexed as

BrainMicrogliaCentral Nervous SystemHomeostasisPhenotypedepletiondevelopmentheterogeneitymicrobiotamicrogliarepopulation

Identifiers

PMID33835613
PMCPMC8225243
OpenAlexW3151367753

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.