Evidence map›Paper›PMID 33054973›Full record

ArticleeLife2020

A MAC2-positive progenitor-like microglial population is resistant to CSF1R inhibition in adult mouse brain.

Lihong Zhan, Li Fan, Lay Kodama, Peter Dongmin Sohn, Man Ying Wong, Gergey Alzaem Mousa, Yungui Zhou, Yaqiao Li, Li Gan

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.0field-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

51 citing papers in PubMed, 80 citations in OpenAlex.

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  17. CCR2Cell reports · 2024
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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

9 authors at 2 institutions in 1 country.

Lihong Zhan *Gladstone Institute of Neurological Diseases, San Francisco, United States.
Li Fan *Helen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.ORCID 0000-0003-1780-6919
Lay KodamaGladstone Institute of Neurological Diseases, San Francisco, United States.
Peter Dongmin SohnGladstone Institute of Neurological Diseases, San Francisco, United States.
Man Ying WongHelen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
Gergey Alzaem MousaHelen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
Yungui ZhouGladstone Institute of Neurological Diseases, San Francisco, United States.
Yaqiao LiGladstone Institute of Neurological Diseases, San Francisco, United States.
Li GanGladstone Institute of Neurological Diseases, San Francisco, United States.ORCID 0000-0003-4600-275X
Gladstone Institutes · USCornell University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007618 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 1985 to 2020
$29.6M
Project 3: Autophagy dysfunction and neuronal activity in FTDU54NS100717 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GAN, LI · 2016 to 2020
$10.8M
Tau acetylation in Alzheimer's diseaseR01AG054214 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI GAN, LI · 2017 to 2021
$3.3M
Molecular mechanisms in progranulin deficient frontotemporal dementiaR01AG051390 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI GAN, LI · 2015 to 2019
$2.5M
BD FACSAria II Flow CytometerS10RR028962 · NCRR · J. DAVID GLADSTONE INSTITUTES · PI CAVROIS, MARIELLE · 2011 to 2011
$544k
Investigating the role of microRNAs in microglia in a mouse model of Alzheimer’s DiseaseF30AG062043 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KODAMA, LAY · 2018 to 2020
$116k
National Institute of Aging F30 AG062043-02NCRR NIH HHS S10 RR028962NIA NIH HHS F30 AG062043NIA NIH HHS R01 AG051390NIA NIH HHS R01 AG054214NIGMS NIH HHS T32 GM007618NIH HHS 1R01AG054214-01A1NIH HHS R01AG051390NIH HHS T32GM007618NIH HHS U54NS100717NINDS NIH HHS U54 NS100717
6 · The paper itself

Abstract

Microglia are the resident myeloid cells in the central nervous system (CNS). The majority of microglia rely on CSF1R signaling for survival. However, a small subset of microglia in mouse brains can survive without CSF1R signaling and reestablish the microglial homeostatic population after CSF1R signaling returns. Using single-cell transcriptomic analysis, we characterized the heterogeneous microglial populations under CSF1R inhibition, including microglia with reduced homeostatic markers and elevated markers of inflammatory chemokines and proliferation. Importantly, MAC2/

Indexed as

AnimalsBrainFemaleGalectin 3HomeostasisMaleMiceMice, Inbred C57BLMicrogliaReceptors, Granulocyte-Macrophage Colony-Stimulating FactorSignal TransductionCsf1r protein, mouseGalectin 3Lgals3 protein, mouseReceptors, Granulocyte-Macrophage Colony-Stimulating Factoradult microglial progenitorscsf1r signalingMac2microgliamicroglia homeostasismousemyeloid cellsneuroscience

Identifiers

PMID33054973
PMCPMC7591254
OpenAlexW3092993329

What OpenQuestion 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 OpenQuestion graph.