Evidence map›Paper›PMID 26779600›Full record

ArticleNature immunology2016

Blimp-1 controls plasma cell function through the regulation of immunoglobulin secretion and the unfolded protein response.

Julie Tellier, Wei Shi, Martina Minnich, Yang Liao, Simon Crawford, Gordon K Smyth, Axel Kallies, Meinrad Busslinger, Stephen L Nutt

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 211 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
211citing papers in PubMed, 2 pooled it
16.5field-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

211 citing papers in PubMed, 2 syntheses or guidelines pooled it, 348 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
  8. Review
  9. Article
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  19. Epstein-Barr virus (EBV) infection causes human germinal center B cell-derived lymphomas in the absence of EBNA2 expression.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  20. Review

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

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

9 authors at 2 institutions in 2 countries.

Julie TellierThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Wei ShiThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Martina MinnichResearch Institute of Molecular Pathology, Vienna Biocenter, Vienna, Austria.
Yang LiaoThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Simon CrawfordSchool of BioSciences, The University of Melbourne, Parkville, Australia.
Gordon K SmythThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.ORCID http://orcid.org/0000-0001-9221-2892
Axel KalliesThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Meinrad BusslingerResearch Institute of Molecular Pathology, Vienna Biocenter, Vienna, Austria.
Stephen L NuttThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
The University of Melbourne · AUResearch Institute of Molecular Pathology · AT

Funding

European Research Council 291740
6 · The paper itself

Abstract

Plasma cell differentiation requires silencing of B cell transcription, while it establishes antibody-secretory function and long-term survival. The transcription factors Blimp-1 and IRF4 are essential for the generation of plasma cells; however, their function in mature plasma cells has remained elusive. We found that while IRF4 was essential for the survival of plasma cells, Blimp-1 was dispensable for this. Blimp-1-deficient plasma cells retained their transcriptional identity but lost the ability to secrete antibody. Blimp-1 regulated many components of the unfolded protein response (UPR), including XBP-1 and ATF6. The overlap in the functions of Blimp-1 and XBP-1 was restricted to that response, with Blimp-1 uniquely regulating activity of the kinase mTOR and the size of plasma cells. Thus, Blimp-1 was required for the unique physiological ability of plasma cells that enables the secretion of protective antibody.

Indexed as

Activating Transcription Factor 6AnimalsCell DifferentiationCell SizeChromatin ImmunoprecipitationDNA-Binding ProteinsEnzyme-Linked Immunosorbent AssayFlow CytometryGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingImmunoglobulinsInterferon Regulatory Factor-4Interferon Regulatory FactorsMiceMice, KnockoutActivating Transcription Factor 6Atf6 protein, mouseDNA-Binding ProteinsImmunoglobulinsInterferon Regulatory Factor-4Interferon Regulatory FactorsmTOR protein, mousePositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseRegulatory Factor X Transcription FactorsTOR Serine-Threonine KinasesTranscription FactorsX-Box Binding Protein 1Xbp1 protein, mouse

Identifiers

PMID26779600
PMCPMC4757736
OpenAlexW2260507520

What OpenQuestion holds

Textmetadata
LicenceTDM
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.