Evidence map›Paper›PMID 23863900›Full record

ArticleBlood2013

Neddylation plays an important role in the regulation of murine and human dendritic cell function.

Nathan Mathewson, Tomomi Toubai, Steven Kapeles, Yaping Sun, Katherine Oravecz-Wilson, Hiroya Tamaki, Ying Wang, Guoqing Hou, Yi Sun, Pavan Reddy

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

53 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Review
  3. [Endogenous neddylation in B cells regulates immune responses in mice].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Neddylation steers the fate of cellular receptors.Experimental & molecular medicine · 2024
    Review
  10. Protein neddylation and its role in health and diseases.Signal transduction and targeted therapy · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Neddylation Regulation of Immune Responses.Research (Washington, D.C.) · 2023
    Review
  18. Article
  19. Article
  20. Association Between Neddylation and Immune Response.Frontiers in cell and developmental biology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Nathan MathewsonDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI; and.
Tomomi Toubai
Steven Kapeles
Yaping Sun
Katherine Oravecz-Wilson
Hiroya Tamaki
Ying Wang
Guoqing Hou
Yi Sun
Pavan Reddy
University of Michigan–Ann Arbor · US

Funding

Targeting antigen presentation to enhance GVL responses after Bone Marrow TransplR01HL090775 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2008 to 2016
$3.4M
Role of APCs in Modulating Donor Natural Tregs Mediated Suppression of GVHDR01AI075284 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2008 to 2012
$1.8M
Development of a Novel Strategy to Prevent Experimental GVHDR01CA143379 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2010 to 2014
$739k
NCI NIH HHS CA143379NCI NIH HHS R01 CA143379NHLBI NIH HHS HL-090775NHLBI NIH HHS R01 HL090775NIAID NIH HHS AI-075284NIAID NIH HHS R01 AI075284
6 · The paper itself

Abstract

Posttranslational protein modifications (PTMs) are necessary for cells to function properly. The role of PTMs in regulating immune responses, specifically those mediated by dendritic cells (DCs), which are critical for both innate and adaptive immunity, is not well understood. Utilizing multiple but complementary approaches, we determined the role of an important but less understood type of PTM, namely, neddylation, in regulating DC functions. Inhibition of neddylation suppressed the release of proinflammatory cytokines by DCs in response to Toll-like receptor, nucleotide oligomerization domain-like receptor, and noninfectious CD40L stimulation. These effects were more profound than those mediated by the proteasome inhibitor bortezomib or a commonly used antiinflammatory agent, dexamethasone. Targeting neddylation also suppressed the ability of DCs to stimulate murine allogeneic T cells in vitro and in vivo and human allogeneic T-cell responses in vitro. Mechanistic studies demonstrated that inhibition of neddylation reduced both canonical and noncanonical nuclear factor-κB (NF-κB) activity. Neddylation inhibition prevented the degradation of inhibitor-κB and thus reduced the translocation and activation of NF-κB, but without perturbation of the mitogen-activated protein kinase/extracellular signal-regulated kinase pathway. Thus, blocking neddylation could be a novel strategy for mitigating immune-mediated disease processes.

Indexed as

Protein Processing, Post-TranslationalAnimalsApoptosisbeta-Transducin Repeat-Containing ProteinsCarrier ProteinsCell LineCyclopentanesCytokinesDendritic CellsEnzyme ActivationExtracellular Signal-Regulated MAP KinasesFemaleHumansI-kappa B ProteinsInflammation MediatorsLipopolysaccharidesbeta-Transducin Repeat-Containing ProteinsCarrier ProteinsCyclopentanesCytokinesExtracellular Signal-Regulated MAP KinasesI-kappa B ProteinsInflammation MediatorsLipopolysaccharidesMitogen-Activated Protein KinasesNEDD8 ProteinNEDD8 protein, humanNedd8 protein, mouseNF-kappa BpevonedistatPyrimidinesSAG protein, mouseUbiquitins

Identifiers

PMID23863900
PMCPMC3778550
OpenAlexW2048263813

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.