Evidence map›Paper›PMID 31968056›Full record

ArticleThe Journal of cell biology2020

The stress-responsive gene GDPGP1/mcp-1 regulates neuronal glycogen metabolism and survival.

Alexander Schulz, Yuichi Sekine, Motunrayo J Oyeyemi, Alexander J Abrams, Manasa Basavaraju, Sung Min Han, Marco Groth, Helen Morrison, Stephen M Strittmatter, Marc Hammarlund

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  3. Glycogen supports glycolytic plasticity in neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Alexander SchulzDepartment of Genetics, Yale University, New Haven, CT.
Yuichi SekineDepartment of Genetics, Yale University, New Haven, CT.
Motunrayo J OyeyemiDepartment of Genetics, Yale University, New Haven, CT.
Alexander J AbramsDepartment of Genetics, Yale University, New Haven, CT.
Manasa BasavarajuDepartment of Genetics, Yale University, New Haven, CT.
Sung Min HanDepartment of Genetics, Yale University, New Haven, CT.
Marco GrothLeibniz Institute on Aging, Fritz Lipmann Institute, Jena, Germany.
Helen MorrisonLeibniz Institute on Aging, Fritz Lipmann Institute, Jena, Germany.
Stephen M StrittmatterDepartment of Neuroscience, Yale University, New Haven, CT.
Marc HammarlundDepartment of Genetics, Yale University, New Haven, CT.
Yale University · USLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
New Mechanisms in Axon RegenerationR01NS094219 · NINDS · YALE UNIVERSITY · PI HAMMARLUND, MARC · 2015 to 2025
$4.0M
Evaluation of Novel Axon Regeneration Targets for Spinal Cord injury TherapyR01NS098817 · NINDS · YALE UNIVERSITY · PI HAMMARLUND, MARC, STRITTMATTER, STEPHEN M · 2016 to 2020
$1.4M
NIH HHS P40 OD010440NINDS NIH HHS R01 NS094219NINDS NIH HHS R01 NS098817
6 · The paper itself

Abstract

Maladaptive responses to stress might play a role in the sensitivity of neurons to stress. To identify novel cellular responses to stress, we performed transcriptional analysis in acutely stressed mouse neurons, followed by functional characterization in Caenorhabditis elegans. In both contexts, we found that the gene GDPGP1/mcp-1 is down-regulated by a variety of stresses. Functionally, the enzyme GDPGP1/mcp-1 protects against stress. Knockdown of GDPGP1 in mouse neurons leads to widespread neuronal cell death. Loss of mcp-1, the single homologue of GDPGP1 in C. elegans, leads to increased degeneration of GABA neurons as well as reduced survival of animals following environmental stress. Overexpression of mcp-1 in neurons enhances survival under hypoxia and protects against neurodegeneration in a tauopathy model. GDPGP1/mcp-1 regulates neuronal glycogen levels, indicating a key role for this metabolite in neuronal stress resistance. Together, our data indicate that down-regulation of GDPGP1/mcp-1 and consequent loss of neuronal glycogen is a maladaptive response that limits neuronal stress resistance and reduces survival.

Indexed as

AnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsDisease Models, AnimalDNA DamageGlucosyltransferasesGlycogenHumansMiceNerve DegenerationNeuronsCaenorhabditis elegans ProteinsGDPGP1 protein, humanGlucosyltransferasesGlycogenmcp-1 protein, C elegans

Identifiers

PMID31968056
PMCPMC7041677
OpenAlexW3001074179

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.