Evidence map›Paper›PMID 28186505›Full record

ArticleCell death and differentiation2017

N-glycosylation of mouse TRAIL-R and human TRAIL-R1 enhances TRAIL-induced death.

Florent Dufour, Thibault Rattier, Sarah Shirley, Gaelle Picarda, Andrei Alexandru Constantinescu, Aymeric Morlé, Al Batoul Zakaria, Guillaume Marcion, Sebastien Causse, Eva Szegezdi and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Nano-TRAIL: a promising path to cancer therapy.Cancer drug resistance (Alhambra, Calif.) · 2023
    Review
  11. Article
  12. TRAIL and its receptors in cardiac diseases.Frontiers in physiology · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. The T/Tn-SpecificCancers · 2021
    Article
  19. Review
  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

20 authors at 5 institutions in 5 countries.

Florent DufourUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Thibault RattierUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Sarah ShirleyUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Gaelle PicardaThe La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.
Andrei Alexandru ConstantinescuUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Aymeric MorléUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Al Batoul ZakariaNanomedicine Lab, Imagery and Therapeutics, EA 4662 Univ. de Bourgogne Franche-Comté, 25030 Besançon Cedex, France.
Guillaume MarcionUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Sebastien CausseUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Eva SzegezdiApoptosis Research Centre, School of Natural Sciences, National University of Ireland, Galway, Ireland.
Dirk Michael ZajoncThe La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.
Renaud SeigneuricUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Gilles GuichardUniversity de Bordeaux, CNRS, IPB, UMR 5248, CBMN, Institut Européen de Chimie et de Biologie, 2 rue Robert Escarpit, 33607 Pessac, France.
Tijani GharbiNanomedicine Lab, Imagery and Therapeutics, EA 4662 Univ. de Bourgogne Franche-Comté, 25030 Besançon Cedex, France.
Fabien PicaudNanomedicine Lab, Imagery and Therapeutics, EA 4662 Univ. de Bourgogne Franche-Comté, 25030 Besançon Cedex, France.
Guillaume HerlemNanomedicine Lab, Imagery and Therapeutics, EA 4662 Univ. de Bourgogne Franche-Comté, 25030 Besançon Cedex, France.
Carmen GarridoUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
Pascal SchneiderDepartment of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland.
Chris Alan BenedictThe La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.
Olivier MicheauUniversity Bourgogne Franche-Comté, LNC UMR866, F-21000 Dijon, France.
La Jolla Institute for Immunology · USCentre Georges François Leclerc · FRCentre National de la Recherche Scientifique · FROllscoil na Gaillimhe – University of Galway · IEUniversity of Lausanne · CH

Funding

The role of TRAIL in immune control of cytomegalovirusR01AI101423 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A · 2013 to 2023
$4.6M
CD4 T cell control of cytomegalovirusR01AI139749 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A · 2019 to 2023
$3.2M
Structural basis of UL141 mediated NK cell inhibition by HCMVR21AI117530 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI ZAJONC, DIRK M · 2015 to 2016
$487k
The role of TRAIL in immune control of cytomegalovirusR56AI101423 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI BENEDICT, CHRISTOPHER A · 2012 to 2012
$435k
NIAID NIH HHS R01 AI101423NIAID NIH HHS R01 AI139749NIAID NIH HHS R21 AI117530NIAID NIH HHS R56 AI101423
6 · The paper itself

Abstract

APO2L/TRAIL (TNF-related apoptosis-inducing ligand) induces death of tumor cells through two agonist receptors, TRAIL-R1 and TRAIL-R2. We demonstrate here that N-linked glycosylation (N-glyc) plays also an important regulatory role for TRAIL-R1-mediated and mouse TRAIL receptor (mTRAIL-R)-mediated apoptosis, but not for TRAIL-R2, which is devoid of N-glycans. Cells expressing N-glyc-defective mutants of TRAIL-R1 and mouse TRAIL-R were less sensitive to TRAIL than their wild-type counterparts. Defective apoptotic signaling by N-glyc-deficient TRAIL receptors was associated with lower TRAIL receptor aggregation and reduced DISC formation, but not with reduced TRAIL-binding affinity. Our results also indicate that TRAIL receptor N-glyc impacts immune evasion strategies. The cytomegalovirus (CMV) UL141 protein, which restricts cell-surface expression of human TRAIL death receptors, binds with significant higher affinity TRAIL-R1 lacking N-glyc, suggesting that this sugar modification may have evolved as a counterstrategy to prevent receptor inhibition by UL141. Altogether our findings demonstrate that N-glyc of TRAIL-R1 promotes TRAIL signaling and restricts virus-mediated inhibition.

Indexed as

Amino Acid SequenceAnimalsApoptosisCell LineCytomegalovirusGlycosylationHCT116 CellsHumansMembrane GlycoproteinsMiceMutagenesis, Site-DirectedNanoparticlesReceptors, TNF-Related Apoptosis-Inducing LigandSequence AlignmentTNF-Related Apoptosis-Inducing LigandTunicamycinMembrane GlycoproteinsReceptors, TNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing LigandTunicamycinUL141 glycoprotein, human cytomegalovirusViral Proteins

Identifiers

PMID28186505
PMCPMC5344210
OpenAlexW2586706543

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.