Evidence map›Paper›PMID 33624208›Full record

ArticleStem cell reviews and reports2021

C3G Regulates STAT3, ERK, Adhesion Signaling, and Is Essential for Differentiation of Embryonic Stem Cells.

Vijay V Vishnu, Bh Muralikrishna, Archana Verma, Sanjeev Chavan Nayak, Divya Tej Sowpati, Vegesna Radha, P Chandra Shekar

Open access · hybridAbstract read
In one paragraph

Article in Stem cell reviews and reports, 2021. 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
0.7field-weighted citation impact, top 32% 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, 12 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 1 institution in 1 country.

Vijay V VishnuCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India.
Bh MuralikrishnaCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India.
Archana VermaCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India.
Sanjeev Chavan NayakCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India.
Divya Tej SowpatiCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India.
Vegesna RadhaCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India. vradha@ccmb.res.in.
P Chandra ShekarCSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, 500 007, India. csp@ccmb.res.in.ORCID http://orcid.org/0000-0002-1737-2105
Centre for Cellular and Molecular Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C3G (RAPGEF1), engaged in multiple signaling pathways, is essential for the early development of the mouse. In this study, we have examined its role in mouse embryonic stem cell self-renewal and differentiation. C3G null cells generated by CRISPR mediated knock-in of a targeting vector exhibited enhanced clonogenicity and long-term self-renewal. They did not differentiate in response to LIF withdrawal when compared to the wild type ES cells and were defective for lineage commitment upon teratoma formation in vivo. Gene expression analysis of C3G KO cells showed misregulated expression of a large number of genes compared with WT cells. They express higher levels of self-renewal factors like KLF4 and ESRRB and show high STAT3 activity, and very low ERK activity compared to WT cells. Reintroduction of C3G expression in a KO line partially reverted expression of ESRRB, and KLF4, and ERK activity similar to that seen in WT cells. The expression of self-renewal factors was persistent for a longer time, and induction of lineage-specific markers was not seen when C3G KO cells were induced to form embryoid bodies. C3G KO cells showed poor adhesion and significantly reduced levels of pFAK, pPaxillin, and Integrin-β1, in addition to downregulation of the cluster of genes involved in cell adhesion, compared to WT cells. Our results show that C3G is essential for the regulation of STAT3, ERK, and adhesion signaling, to maintain pluripotency of mouse embryonic stem cells and enable their lineage commitment for differentiation.

Indexed as

Cell DifferentiationMouse Embryonic Stem CellsSignal TransductionAnimalsExtracellular Signal-Regulated MAP KinasesGuanine Nucleotide-Releasing Factor 2Leukemia Inhibitory FactorMiceSTAT3 Transcription FactorExtracellular Signal-Regulated MAP KinasesGuanine Nucleotide-Releasing Factor 2Leukemia Inhibitory FactorRapgef1 protein, mouseStat3 protein, mouseSTAT3 Transcription FactorAdhesionC3GDifferentiationE14Tg2a mouse embryonic stem cellsERKKnock outRAPGEF1Self-renewalSTAT3Transcriptome analysis

Identifiers

PMID33624208
PMCPMC8372029
OpenAlexW3129342626

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.