Evidence map›Paper›PMID 28130495›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

The Molecular Basis for the Lack of Inflammatory Responses in Mouse Embryonic Stem Cells and Their Differentiated Cells.

William D'Angelo, Chandan Gurung, Dhiraj Acharya, Bohan Chen, Natalya Ortolano, Vivian Gama, Fengwei Bai, Yan-Lin Guo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Mouse Trophoblast Stem Cells Are Deficient in TNFα-Activated NFκB Signaling Pathway and Inflammatory Response.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
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  14. Novel function ofIranian journal of basic medical sciences · 2021
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  17. Explaining Pathogenicity of Congenital Zika and Guillain-Barré Syndromes: Does Dysregulation of RNA Editing Play a Role?BioEssays : news and reviews in molecular, cellular and developmental biology · 2019
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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

8 authors at 2 institutions in 1 country.

William D'AngeloDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and.
Chandan GurungDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and.ORCID 0000-0003-2411-0733
Dhiraj AcharyaDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and.
Bohan ChenDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and.ORCID 0000-0002-9781-2982
Natalya OrtolanoDepartment of Cell and Developmental Biology, Vanderbilt Center for Stem Cell Biology, Vanderbilt University School of Medicine, Nashville, TN 37240.
Vivian GamaDepartment of Cell and Developmental Biology, Vanderbilt Center for Stem Cell Biology, Vanderbilt University School of Medicine, Nashville, TN 37240.
Fengwei BaiDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and.
Yan-Lin GuoDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406; and yanlin.guo@usm.edu.ORCID 0000-0001-6116-2247
University of Southern Mississippi · USVanderbilt University · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
Apoptotic Proteins as Molecular Modulators of Stem Cell FateR00CA178190 · NCI · VANDERBILT UNIVERSITY · PI GAMA, VIVIAN · 2015 to 2017
$747k
Embryonic stem cell-based fibroblast model of innate immunity developmentR15GM109299 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI GUO, YAN-LIN · 2014 to 2014
$354k
NCI NIH HHS R00 CA178190NICHD NIH HHS T32 HD007502NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM109299
6 · The paper itself

Abstract

We reported previously that mouse embryonic stem cells do not have a functional IFN-based antiviral mechanism. The current study extends our investigation to the inflammatory response in mouse embryonic stem cells and mouse embryonic stem cell-differentiated cells. We demonstrate that LPS, TNF-α, and viral infection, all of which induce robust inflammatory responses in naturally differentiated cells, failed to activate NF-κB, the key transcription factor that mediates inflammatory responses, and were unable to induce the expression of inflammatory genes in mouse embryonic stem cells. Similar results were obtained in human embryonic stem cells. In addition to the inactive state of NF-κB, the deficiency in the inflammatory response in mouse embryonic stem cells is also attributed to the lack of functional receptors for LPS and TNF-α. In vitro differentiation can trigger the development of the inflammatory response mechanism, as indicated by the transition of NF-κB from its inactive to active state. However, a limited response to TNF-α and viral infection, but not to LPS, was observed in mouse embryonic stem cell-differentiated fibroblasts. We conclude that the inflammatory response mechanism is not active in mouse embryonic stem cells, and in vitro differentiation promotes only partial development of this mechanism. Together with our previous studies, the findings described in this article demonstrate that embryonic stem cells are fundamentally different from differentiated somatic cells in their innate immunity, which may have important implications in developmental biology, immunology, and embryonic stem cell-based regenerative medicine.

Indexed as

AnimalsCell DifferentiationChikungunya FeverChikungunya virusEmbryonic Stem CellsImmunityInflammationInterferonsLipopolysaccharidesMiceMice, Inbred DBANF-kappa BRAW 264.7 CellsTumor Necrosis Factor-alphaVirus DiseasesInterferonsLipopolysaccharidesNF-kappa BTumor Necrosis Factor-alpha

Identifiers

PMID28130495
PMCPMC5321812
OpenAlexW2584931446

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.