Evidence map›Paper›PMID 27385127›Full record

ArticleJournal of neurochemistry2017

Reduced sterol regulatory element-binding protein (SREBP) processing through site-1 protease (S1P) inhibition alters oligodendrocyte differentiation in vitro.

Hubert Monnerie, Micah Romer, Brigid K Jensen, John S Millar, Kelly L Jordan-Sciutto, Sangwon F Kim, Judith B Grinspan

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 34 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

7 authors at 2 institutions in 1 country.

Hubert MonnerieDepartment of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Micah RomerDepartment of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Brigid K JensenDepartment of Neuroscience, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
John S MillarInstitute of Diabetes, Obesity and Metabolism, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Kelly L Jordan-SciuttoDepartment of Pathology, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sangwon F KimDepartment of Psychiatry, Center for Neurobiology and Behavior, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Judith B GrinspanDepartment of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

TRANSGENIC MOUSE MODELS OF MENTAL RETARDATIONP30HD026979 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI ROBERTS, TIMOTHY P · 1990 to 2015
$15.3M
Oligodendrocyte damage and dysfunction in HIV associated neurocognitive disorderR01MH098742 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI JUDITH B GRINSPAN, Kelly L Jordan-Sciutto · 2012 to 2026
$9.0M
Secoisolariciresinol diglucoside to mitigate inflammation and toxicity in HANDR01MH106967 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI JORDAN-SCIUTTO, KELLY L, PERSIDSKY, YURI · 2015 to 2019
$3.3M
TRAINING IN NEUROVIROLOGY AND NEUROIMMUNOLOGYT32NS007180 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI WEISS, SUSAN R · 1985 to 2018
$2.8M
NICHD NIH HHS P30 HD026979NIMH NIH HHS R01 MH098742NIMH NIH HHS R01 MH106967NINDS NIH HHS T32 NS007180
6 · The paper itself

Abstract

The formation of the myelin membrane of the oligodendrocyte in the CNS is a fundamental process requiring the coordinated synthesis of many different components. The myelin membrane is particularly rich in lipids, however, the regulation of this lipid synthesis is not understood. In other cell types, including Schwann cells, the myelin-forming cells of the PNS, lipid synthesis is tightly regulated by the sterol regulatory element-binding protein (SREBP) family of transcription factors, but this has not been previously shown in oligodendrocytes. We investigated SREBPs' role during oligodendrocyte differentiation in vitro. Both SREBP-1 and SREBP-2 were expressed in oligodendrocyte precursor cells and differentiating oligodendrocytes. Using the selective site-1 protease (S1P) inhibitor PF-429242, which inhibits the cleavage of SREBP precursor forms into mature forms, we found that preventing SREBP processing inhibited process growth and reduced the expression level of myelin basic protein, a major component of myelin. Further, process extension deficits could be rescued by the addition of exogenous cholesterol. Blocking SREBP processing reduced mRNA transcription and protein levels of SREBP target genes involved in both the fatty acid and the cholesterol synthetic pathways. Furthermore, de novo levels and total levels of cholesterol synthesis were greatly diminished when SREBP processing was inhibited. Together these results indicate that SREBPs are important regulators of oligodendrocyte maturation and that perturbation of their activity may affect myelin formation and integrity. Cover Image for this issue: doi: 10.1111/jnc.13781.

Indexed as

AnimalsAnimals, NewbornCell DifferentiationCells, CulturedFemaleMaleMiceOligodendrogliaProprotein ConvertasesPyrrolidinesSerine EndopeptidasesSterol Regulatory Element Binding Proteinsmembrane-bound transcription factor peptidase, site 1PF-429242Proprotein ConvertasesPyrrolidinesSerine EndopeptidasesSterol Regulatory Element Binding Proteinslipidmyelinoligodendrocyteprocess growthSREBP

Identifiers

PMID27385127
PMCPMC5548300
OpenAlexW2471167444

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.