Evidence map›Paper›PMID 36945622›Full record

ArticlebioRxiv : the preprint server for biology2023

Jedi-1/MEGF12-mediated phagocytosis controls the pro-neurogenic properties of microglia in the ventricular-subventricular zone.

Vivianne E Morrison, Matthew G Houpert, Jonathan B Trapani, Asa A Brockman, Philip J Kingsley, Ketaki A Katdare, Hillary M Layden, Gabriela Nguena-Jones, Alexandra J Trevisan, Kathleen A Maguire-Zeiss and 4 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Vivianne E MorrisonVanderbilt University Department of Biochemistry.
Matthew G HoupertVanderbilt University Department of Biochemistry.
Jonathan B TrapaniVanderbilt University Department of Biochemistry.
Asa A BrockmanVanderbilt University Department of Cell and Developmental Biology.
Philip J KingsleyVanderbilt University Department of Biochemistry.
Ketaki A KatdareVanderbilt Brain Institute.
Hillary M LaydenVanderbilt University Department of Biochemistry.
Gabriela Nguena-JonesVanderbilt University Department of Biochemistry.
Alexandra J TrevisanVanderbilt University Department of Biochemistry.
Kathleen A Maguire-ZeissGeorgetown University Department of Neuroscience.
Lawrence J MarnettVanderbilt University Department of Biochemistry.
Gregory J BixTulane University Center for Clinical Neuroscience Research.
Rebecca A IhrieVanderbilt University Department of Cell and Developmental Biology.
Bruce D CarterVanderbilt University Department of Biochemistry.
Allen Institute for Brain Science · USVanderbilt University · USTulane University · USGeorgetown University · USSt. Jude Children's Research Hospital · US

Funding

MULTIDISCIPLINARY TRAINING IN MOLECULAR ENDOCRINOLOGYT32DK007563 · NIDDK · VANDERBILT UNIVERSITY · PI Richard M O'Brien · 1988 to 2026
$15.9M
Identifying mTOR Dependent Periods During Brain DevelopmentR01NS118580 · NINDS · VANDERBILT UNIVERSITY · PI ESS, KEVIN C, IHRIE, REBECCA A · 2020 to 2024
$2.1M
PAR-1 Signaling and HANDR01NS083410 · NINDS · GEORGETOWN UNIVERSITY · PI CONANT, KATHERINE E, MAGUIRE-ZEISS, KATHLEEN ANNE · 2013 to 2017
$1.9M
The role of the glial engulfment receptor Jedi1 in regulating sensory neuron functionR01NS102365 · NINDS · VANDERBILT UNIVERSITY · PI CARTER, BRUCE D · 2018 to 2022
$1.7M
Loss of Jedi-1 impairs microglia phagocytosis, resulting in reduced postnatal neurogenesis in the ventricular-subventricular zone.F32HD107930 · NICHD · TULANE UNIVERSITY OF LOUISIANA · PI MORRISON, VIVIANNE E · 2022 to 2022
$77k
NICHD NIH HHS F32 HD107930NIDDK NIH HHS T32 DK007563NINDS NIH HHS R01 NS083410NINDS NIH HHS R01 NS102365NINDS NIH HHS R01 NS118580
6 · The paper itself

Abstract

Microglia are the primary phagocytes in the central nervous system and are responsible for clearing dead cells generated during development or disease. The phagocytic process shapes the phenotype of the microglia, which affects the local environment. A unique population of microglia reside in the ventricular-subventricular zone (V-SVZ) of neonatal mice, but how they influence this neurogenic niche is not well-understood. Here, we demonstrate that phagocytosis creates a pro-neurogenic microglial phenotype in the V-SVZ and that these microglia phagocytose apoptotic cells via the engulfment receptor Jedi-1. Deletion of

Indexed as

aging/neurodegenerationMicroglianeuroinflammationphagocytosissequencingTREM2

Identifiers

PMID36945622
PMCPMC10028845
OpenAlexW4323355267

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.