Evidence map›Paper›PMID 25221943›Full record

ArticlePloS one2014

mTORC1 is essential for early steps during Schwann cell differentiation of amniotic fluid stem cells and regulates lipogenic gene expression.

Andrea Preitschopf, Kongzhao Li, David Schörghofer, Katharina Kinslechner, Birgit Schütz, Ha Thi Thanh Pham, Margit Rosner, Gabor Jozsef Joo, Clemens Röhrl, Thomas Weichhart and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Amniotic Fluid Stem Cells: What They Are and What They Can Become.Current stem cell research & therapy · 2023
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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

14 authors at 2 institutions in 2 countries.

Andrea PreitschopfInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Kongzhao LiInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria; Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
David SchörghoferInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Katharina KinslechnerInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Birgit SchützInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Ha Thi Thanh PhamInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Margit RosnerInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Gabor Jozsef Joo1st Department of Obstetrics and Gynaecology, Semmelweis University Medical School, Budapest, Hungary.
Clemens RöhrlInstitute of Medical Chemistry, Medical University of Vienna, Vienna, Austria.
Thomas WeichhartInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Herbert StanglInstitute of Medical Chemistry, Medical University of Vienna, Vienna, Austria.
Gert LubecDepartment of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Markus HengstschlägerInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Mario MikulaInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATSemmelweis University · HU

Funding

Austrian Science Fund FWF P 25336
6 · The paper itself

Abstract

Schwann cell development is hallmarked by the induction of a lipogenic profile. Here we used amniotic fluid stem (AFS) cells and focused on the mechanisms occurring during early steps of differentiation along the Schwann cell lineage. Therefore, we initiated Schwann cell differentiation in AFS cells and monitored as well as modulated the activity of the mechanistic target of rapamycin (mTOR) pathway, the major regulator of anabolic processes. Our results show that mTOR complex 1 (mTORC1) activity is essential for glial marker expression and expression of Sterol Regulatory Element-Binding Protein (SREBP) target genes. Moreover, SREBP target gene activation by statin treatment promoted lipogenic gene expression, induced mTORC1 activation and stimulated Schwann cell differentiation. To investigate mTORC1 downstream signaling we expressed a mutant S6K1, which subsequently induced the expression of the Schwann cell marker S100b, but did not affect lipogenic gene expression. This suggests that S6K1 dependent and independent pathways downstream of mTORC1 drive AFS cells to early Schwann cell differentiation and lipogenic gene expression. In conclusion our results propose that future strategies for peripheral nervous system regeneration will depend on ways to efficiently induce the mTORC1 pathway.

Indexed as

Amniotic FluidAnimalsCell DifferentiationGene Expression RegulationHumansLipogenesisMechanistic Target of Rapamycin Complex 1Mice, Inbred C57BLMultiprotein ComplexesSchwann CellsSignal TransductionStem CellsTOR Serine-Threonine KinasesMechanistic Target of Rapamycin Complex 1MTOR protein, humanMultiprotein ComplexesTOR Serine-Threonine Kinases

Identifiers

PMID25221943
PMCPMC4164523
OpenAlexW2088667782

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.