Evidence map›Paper›PMID 29113698›Full record

ArticleJournal of neuroimmunology2019

The control of oligodendrocyte bioenergetics by interferon-gamma (IFN-γ) and Src homology region 2 domain-containing phosphatase-1 (SHP-1).

Scott B Minchenberg, Paul T Massa

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroimmunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.1field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Emerging cellular themes in leukodystrophies.Frontiers in cell and developmental biology · 2022
    Review
  8. Two DuplicatedFrontiers in immunology · 2021
    Article
  9. Review
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.

Scott B MinchenbergDepartment of Microbiology and Immunology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, NY, United States.
Paul T MassaDepartment of Microbiology and Immunology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, NY, United States; Department of Neurology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, NY, United States. Electronic address: MassaP@upstate.edu.
SUNY Upstate Medical University · US

Funding

Function of SHP-1 in oligodendrocytesR01NS073810 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI MASSA, PAUL T · 2012 to 2015
$1.1M
Oligodendrocyte-Specific Regulation of Mitochondrial FunctionF30NS095498 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI MINCHENBERG, SCOTT BRIAN · 2016 to 2018
$105k
NINDS NIH HHS F30 NS095498NINDS NIH HHS R01 NS073810
6 · The paper itself

Abstract

Glycolysis and mitochondrial respiration are essential for oligodendrocyte metabolism in both the developing and adult CNS. Based on recent reports on the effects of the proinflammatory cytokine IFN-γ on metabolism and on oligodendrocytes, we addressed whether IFN-γ may affect oligodendrocyte bioenergetics in ways relevant to CNS disease. Oligodendrocytes of mice treated with IFN-γ showed significant reductions in aerobic glycolysis and mitochondrial respiration. As expected, IFN-γ treatment led to the induction of STAT1 in oligodendrocytes indicating active signaling into these cells. To determine the direct effects of IFN-γ on oligodendrocyte metabolism, cultured oligodendrocytes were treated with IFN-γ in vitro, which resulted in suppression of glycolysis similar to oligodendrocytes of animals treated with IFN-γ in vivo. Mice lacking SHP-1, a key regulator of IFN-γ and STAT1 signaling in CNS glia, had high constitutive levels of STAT1 and decreased aerobic glycolysis and mitochondrial respiration rates relative to wild type mouse oligodendrocytes. Together, these data show that IFN-γ and SHP-1 control oligodendrocyte bioenergetics in ways that may relate to the role of this cytokine in CNS disease.

Indexed as

AnimalsCells, CulturedCentral Nervous SystemEnergy MetabolismEnzyme ActivationEnzyme InductionFemaleGlycolysisInterferon-gammaMaleMiceMice, Inbred C3HMice, Neurologic MutantsOligodendrogliaOxidative PhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 6Interferon-gammaProtein Tyrosine Phosphatase, Non-Receptor Type 6Ptpn6 protein, mouseStat1 protein, mouseSTAT1 Transcription FactorCytokine signalingGlycolysisInterferon gamma [IFN-γ]MetabolismMitochondriaSHP-1 [PTPN6]

Identifiers

PMID29113698
PMCPMC5924629
OpenAlexW2765549544

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.