Evidence map›Paper›PMID 23710283›Full record

ArticleOxidative medicine and cellular longevity2013

Adaptive redox response of mesenchymal stromal cells to stimulation with lipopolysaccharide inflammagen: mechanisms of remodeling of tissue barriers in sepsis.

Nikolai V Gorbunov, Bradley R Garrison, Dennis P McDaniel, Min Zhai, Pei-Jyun Liao, Dilber Nurmemet, Juliann G Kiang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  8. State of the field: cellular and exosomal therapeutic approaches in vascular regeneration.American journal of physiology. Heart and circulatory physiology · 2022
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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.

Nikolai V GorbunovRadiation Combined Injury Program, Armed Forces Radiobiology Research Institute, Bethesda, MD 20889-1402, USA. nikolaiv.gorbunov@gmail.com
Bradley R Garrison
Dennis P McDaniel
Min Zhai
Pei-Jyun Liao
Dilber Nurmemet
Juliann G Kiang
Armed Forces Institute of Pathology · USUniformed Services University of the Health Sciences · US

Funding

Ciprofloxacin enhances DNA repair capacity after radiation combined injuryR33AI080553 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI KIANG, JULIANN GONG · 2010 to 2012
$1.1M
Ciprofloxacin enhances DNA repair capacity after radiation combined injuryR21AI080553 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI KIANG, JULIANN GONG · 2008 to 2009
$378k
NIAID NIH HHS R21/33AI080553NIAID NIH HHS R33 AI080553NIAID NIH HHS Y01 AI005045NIAID NIH HHS Y1-AI-5045-04
6 · The paper itself

Abstract

Acute bacterial inflammation is accompanied by excessive release of bacterial toxins and production of reactive oxygen and nitrogen species (ROS and RNS), which ultimately results in redox stress. These factors can induce damage to components of tissue barriers, including damage to ubiquitous mesenchymal stromal cells (MSCs), and thus can exacerbate the septic multiple organ dysfunctions. The mechanisms employed by MSCs in order to survive these stress conditions are still poorly understood and require clarification. In this report, we demonstrated that in vitro treatment of MSCs with lipopolysaccharide (LPS) induced inflammatory responses, which included, but not limited to, upregulation of iNOS and release of RNS and ROS. These events triggered in MSCs a cascade of responses driving adaptive remodeling and resistance to a "self-inflicted" oxidative stress. Thus, while MSCs displayed high levels of constitutively present adaptogens, for example, HSP70 and mitochondrial Sirt3, treatment with LPS induced a number of adaptive responses that included induction and nuclear translocation of redox response elements such as NFkB, TRX1, Ref1, Nrf2, FoxO3a, HO1, and activation of autophagy and mitochondrial remodeling. We propose that the above prosurvival pathways activated in MSCs in vitro could be a part of adaptive responses employed by stromal cells under septic conditions.

Indexed as

AnimalsCell NucleusFluorescent Antibody TechniqueInflammationLipopolysaccharidesMesenchymal Stem CellsMiceMitochondriaNF-kappa BNitric OxideNitric Oxide Synthase Type IIOxidation-ReductionPhagosomesReactive Nitrogen SpeciesReactive Oxygen SpeciesResponse ElementsLipopolysaccharidesNF-kappa BNitric OxideNitric Oxide Synthase Type IIReactive Nitrogen SpeciesReactive Oxygen SpeciesThioredoxinsTranscription Factor RelA

Identifiers

PMID23710283
PMCPMC3654342
OpenAlexW2084077039

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.