Evidence map›Paper›PMID 24945434›Full record

ArticlePloS one2014

STAT3 modulation to enhance motor neuron differentiation in human neural stem cells.

Rajalaxmi Natarajan, Vinamrata Singal, Richard Benes, Junling Gao, Hoi Chan, Haijun Chen, Yongjia Yu, Jia Zhou, Ping Wu

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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

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  13. STAT3 in Skeletal Muscle Function and Disorders.International journal of molecular sciences · 2018
    Review
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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

9 authors at 1 institution in 1 country.

Rajalaxmi NatarajanDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Vinamrata SingalDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Richard BenesDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Junling GaoDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Hoi ChanDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Haijun ChenDepartment of Pharmacology & Toxicology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Yongjia YuDepartment of Radiation Oncology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Jia ZhouDepartment of Pharmacology & Toxicology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Ping WuDepartment of Neuroscience and Cell Biology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
The University of Texas Medical Branch at Galveston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury or amyotrophic lateral sclerosis damages spinal motor neurons and forms a glial scar, which prevents neural regeneration. Signal transducer and activator of transcription 3 (STAT3) plays a critical role in astrogliogenesis and scar formation, and thus a fine modulation of STAT3 signaling may help to control the excessive gliogenic environment and enhance neural repair. The objective of this study was to determine the effect of STAT3 inhibition on human neural stem cells (hNSCs). In vitro hNSCs primed with fibroblast growth factor 2 (FGF2) exhibited a lower level of phosphorylated STAT3 than cells primed by epidermal growth factor (EGF), which correlated with a higher number of motor neurons differentiated from FGF2-primed hNSCs. Treatment with STAT3 inhibitors, Stattic and Niclosamide, enhanced motor neuron differentiation only in FGF2-primed hNSCs, as shown by increased homeobox gene Hb9 mRNA levels as well as HB9+ and microtubule-associated protein 2 (MAP2)+ co-labeled cells. The increased motor neuron differentiation was accompanied by a decrease in the number of glial fibrillary acidic protein (GFAP)-positive astrocytes. Interestingly, Stattic and Niclosamide did not affect the level of STAT3 phosphorylation; rather, they perturbed the nuclear translocation of phosphorylated STAT3. In summary, we demonstrate that FGF2 is required for motor neuron differentiation from hNSCs and that inhibition of STAT3 further increases motor neuron differentiation at the expense of astrogliogenesis. Our study thus suggests a potential benefit of targeting the STAT3 pathway for neurotrauma or neurodegenerative diseases.

Indexed as

Cell DifferentiationAstrocytesCell LineCell NucleusCell SurvivalCyclic S-OxidesFibroblast Growth Factor 2Glial Fibrillary Acidic ProteinHumansMotor NeuronsNeural Stem CellsNiclosamidePhosphorylationPhosphotyrosineProtein TransportSTAT3 Transcription FactorCyclic S-OxidesFibroblast Growth Factor 2Glial Fibrillary Acidic ProteinNiclosamidePhosphotyrosineSTAT3 protein, humanSTAT3 Transcription Factorstattic

Identifiers

PMID24945434
PMCPMC4063761
OpenAlexW1987653030

What OpenQuestion holds

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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.