Evidence map›Paper›PMID 24441789›Full record

ArticleNature immunology2014

The unfolded-protein-response sensor IRE-1α regulates the function of CD8α+ dendritic cells.

Fabiola Osorio, Simon J Tavernier, Eik Hoffmann, Yvan Saeys, Liesbet Martens, Jessica Vetters, Iris Delrue, Riet De Rycke, Eef Parthoens, Philippe Pouliot and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

157 citing papers in PubMed, 224 citations in OpenAlex.

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  20. Endoplasmic reticulum stress in non-small cell lung cancer.American journal of cancer research · 2025
    Review

97 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Fabiola Osorio1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium. [4].
Simon J Tavernier1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium. [4].
Eik Hoffmann1] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [2] Unit of Molecular Signal Transduction in Inflammation, VIB Inflammation Research Center, Ghent, Belgium.
Yvan Saeys1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Liesbet Martens1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Jessica Vetters1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Iris Delrue1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Riet De RyckeMicroscopy Core Facility, VIB Inflammation Research Center, Ghent, Belgium.
Eef ParthoensMicroscopy Core Facility, VIB Inflammation Research Center, Ghent, Belgium.
Philippe Pouliot1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Takao IwawakiAdvanced Scientific Research Leaders Development Unit, Gunma University, Gunma, Japan.
Sophie Janssens1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium. [4].
Bart N Lambrecht1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent, Belgium. [2] GROUP-ID Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium. [4] Department of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands. [5].
VIB-UGent Center for Inflammation Research · BEGhent University Hospital · BEGunma University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the unfolded protein response (UPR) and endoplasmic reticulum (ER) stress in homeostasis of the immune system is incompletely understood. Here we found that dendritic cells (DCs) constitutively activated the UPR sensor IRE-1α and its target, the transcription factor XBP-1, in the absence of ER stress. Loss of XBP-1 in CD11c+ cells led to defects in phenotype, ER homeostasis and antigen presentation by CD8α+ conventional DCs, yet the closely related CD11b+ DCs were unaffected. Whereas the dysregulated ER in XBP-1-deficient DCs resulted from loss of XBP-1 transcriptional activity, the phenotypic and functional defects resulted from regulated IRE-1α-dependent degradation (RIDD) of mRNAs, including those encoding CD18 integrins and components of the major histocompatibility complex (MHC) class I machinery. Thus, a precisely regulated feedback circuit involving IRE-1α and XBP-1 controls the homeostasis of CD8α+ conventional DCs.

Indexed as

Protein UnfoldingAnimalsAntigen PresentationCD8 AntigensCross-PrimingDendritic CellsDNA-Binding ProteinsEndoplasmic ReticulumEndoribonucleasesFeedback, PhysiologicalHomeostasisImmunoblottingImmunohistochemistryMiceMice, Inbred C57BLMice, KnockoutCD8alpha antigenCD8 AntigensDNA-Binding ProteinsEndoribonucleasesErn1 protein, mouseProtein Serine-Threonine KinasesRegulatory Factor X Transcription FactorsTranscription FactorsX-Box Binding Protein 1Xbp1 protein, mouse

Identifiers

PMID24441789
OpenAlexW1530495975

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.