Evidence map›Paper›PMID 24676276›Full record

ArticleJournal of leukocyte biology2014

The mechanisms of up-regulation of dendritic cell activity by oxidative stress.

Ibrahim Batal, Jamil Azzi, Marwan Mounayar, Rozita Abdoli, Robert Moore, Jack Y Lee, Florencia Rosetti, Chang Wang, Paolo Fiorina, Robert Sackstein and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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  13. Homocysteine and psoriasis.Bioscience reports · 2019
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  19. Novel Application of Localized Nanodelivery of Anti-Interleukin-6 Protects Organ Transplant From Ischemia-Reperfusion Injuries.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2017
    Article
  20. Article
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

12 authors at 2 institutions in 1 country.

Ibrahim BatalTransplantation Research Center, Departments of Pathology and.
Jamil AzziTransplantation Research Center.
Marwan MounayarTransplantation Research Center.
Rozita AbdoliTransplantation Research Center.
Robert MooreTransplantation Research Center.
Jack Y LeeDermatology, and.
Florencia RosettiDepartments of Pathology and.
Chang WangRenal Division, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Paolo FiorinaTransplantation Research Center.
Robert SacksteinDermatology, and.
Takaharu IchimuraRenal Division, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Reza AbdiTransplantation Research Center, rabdi@rics.bwh.harvard.edu.
Brigham and Women's Hospital · USHarvard University · US

Funding

REGULATION OF LACTOSAMINYL GLYCAN BIOSYNTHESIS IN HEMATOPOIETIC CELLSP01HL107146 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKSTEIN, ROBERT · 2011 to 2017
$17.7M
Ischemia-reperfusion injury in transplantation: novel cytoprotection strategiesR01AI091930 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI ABDI, REZA · 2011 to 2015
$2.1M
NHLBI NIH HHS P01 HL107146NIAID NIH HHS R01 AI091930NIAID NIH HHS R01-AI091930-03
6 · The paper itself

Abstract

Whereas DC have increasingly been recognized for their role in activating the inflammatory cascades during IRIs, the mechanisms by which oxidative stress enhances DC activation remain to be explored. We examined the role of oxidative stress on two important features of DC: T cell activation and trafficking. Bone marrow-derived OS-DC were compared with untreated DC. DC exposed to oxidative stress augmented allogeneic T cell proliferation and showed increased migration in a chemotaxis chamber. These results were confirmed by using hypoxanthine and xanthine oxidase as another inducer of oxidative stress. We used OT-II and OT-I mice to assess the effect of oxidative stress on DC activation of OVA-specific CD4(+) and CD8(+) T cells, respectively. Oxidative stress increased DC capacity to promote OVA-specific CD4(+) T cell activity, demonstrated by an increase in their proliferation and production of IFN-γ, IL-6, and IL-2 proinflammatory cytokines. Whereas oxidative stress increased the DC ability to stimulate IFN-γ production by OVA-specific CD8(+) T cells, cellular proliferation and cytotoxicity were not affected. Compared with untreated DC, oxidative stress significantly reduced the capacity of DC to generate T(regs), which were restored by using anti-IL-6. With regard to DC trafficking, whereas oxidative stress increased DC expression of p-Akt and p-NF-κB, targeting PI3Kγ and NF-κB pathways abrogated the observed increase in DC migration. Our data propose novel insights on the activation of DC by oxidative stress and provide rationales for targeted therapies, which can potentially attenuate IRI.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell MovementCytokinesDendritic CellsMiceMice, Inbred BALB CMice, KnockoutNF-kappa BOxidative StressPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktT-Lymphocytes, RegulatoryUp-RegulationCytokinesNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktH2O2migrationT cell activation

Identifiers

PMID24676276
PMCPMC4101089
OpenAlexW2132394487

What OpenQuestion holds

Textmetadata
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.