Evidence map›Paper›PMID 32848054›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Age-related loss of neural stem cell O-GlcNAc promotes a glial fate switch through STAT3 activation.

Charles W White, Xuelai Fan, Jason C Maynard, Elizabeth G Wheatley, Gregor Bieri, Julien Couthouis, Alma L Burlingame, Saul A Villeda

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 2 pooled it
10.2field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 2 syntheses or guidelines pooled it, 107 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Charles W WhiteDepartment of Anatomy, University of California, San Francisco, CA 94143.
Xuelai FanDepartment of Anatomy, University of California, San Francisco, CA 94143.
Jason C MaynardMass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158.ORCID 0000-0001-7838-5420
Elizabeth G WheatleyDepartment of Anatomy, University of California, San Francisco, CA 94143.ORCID 0000-0001-5459-8827
Gregor BieriDepartment of Anatomy, University of California, San Francisco, CA 94143.ORCID 0000-0003-0737-231X
Julien CouthouisDepartment of Genetics, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0002-2378-4595
Alma L BurlingameMass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158.ORCID 0000-0002-8403-7307
Saul A VilledaDepartment of Anatomy, University of California, San Francisco, CA 94143; Saul.Villeda@ucsf.edu.
University of California, San Francisco · USStanford University · US

Funding

Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
Role of O-GlcNAcylation in Regulating Neurodegeneration in Aging and Alzheimer’s DiseaseRF1AG062357 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2018 to 2018
$2.0M
Investigating the pro-aging role of B2M and MHC molecules on regenerative and cognitive function in the brainR01AG055797 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2017 to 2021
$1.6M
The Role of OGT in Regulating Hippocampal Neuronal Integrity and Cognition with AgeF31AG050415 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WHEATLEY, ELIZABETH GRACE · 2015 to 2017
$115k
Howard Hughes Medical InstituteNIA NIH HHS F31 AG050415NIA NIH HHS R01 AG055797NIA NIH HHS RF1 AG062357NIGMS NIH HHS P41 GM103481
6 · The paper itself

Abstract

Increased neural stem cell (NSC) quiescence is a major determinant of age-related regenerative decline in the adult hippocampus. However, a coextensive model has been proposed in which division-coupled conversion of NSCs into differentiated astrocytes restrict the stem cell pool with age. Here we report that age-related loss of the posttranslational modification, O-linked β-

Indexed as

AgingAnimalsCell DifferentiationCell ProliferationComputational BiologyGene Expression RegulationGlucosamineHippocampusMiceNeural Stem CellsNeurogenesisNeurogliaSequence Analysis, RNASTAT3 Transcription FactorGlucosamineN-acetylglucopyranosylamineStat3 protein, mouseSTAT3 Transcription Factoraginggliogenesisneural stem cellsneurogenesisO-GlcNAcylation

Identifiers

PMID32848054
PMCPMC7486730
OpenAlexW3080531673

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.