Evidence map›Paper›PMID 26773039›Full record

ArticleBlood2016

B-cell survival and development controlled by the coordination of NF-κB family members RelB and cRel.

Jonathan V Almaden, Yi C Liu, Edward Yang, Dennis C Otero, Harry Birnbaum, Jeremy Davis-Turak, Masataka Asagiri, Michael David, Ananda W Goldrath, Alexander Hoffmann

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 48 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Jonathan V AlmadenSignaling Systems Laboratory and San Diego Center for Systems Biology, University of California, San Diego, La Jolla, CA;
Yi C LiuSignaling Systems Laboratory and San Diego Center for Systems Biology, University of California, San Diego, La Jolla, CA; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA;ORCID http://orcid.org/0000-0003-1372-2101
Edward YangDivision of Biological Sciences, University of California, San Diego, La Jolla, CA; and.
Dennis C OteroDivision of Biological Sciences, University of California, San Diego, La Jolla, CA; and.
Harry BirnbaumDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA;
Jeremy Davis-TurakSignaling Systems Laboratory and San Diego Center for Systems Biology, University of California, San Diego, La Jolla, CA;
Masataka AsagiriInnovation Center for Immunoregulation and Therapeutics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Michael DavidDivision of Biological Sciences, University of California, San Diego, La Jolla, CA; and.
Ananda W GoldrathDivision of Biological Sciences, University of California, San Diego, La Jolla, CA; and.
Alexander HoffmannSignaling Systems Laboratory and San Diego Center for Systems Biology, University of California, San Diego, La Jolla, CA; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA;
University of California San Diego · USUniversity of California, Los Angeles · USKyoto University · JP

Funding

SYNTHETIC SYSTEMSP50GM085764 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HASTY, JEFF M, IDEKER, TREY · 2010 to 2018
$23.3M
T cell maintenance: molecular mediators of the TCR-derived survival signalR01AI067545 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GOLDRATH, ANANDA W · 2006 to 2021
$6.1M
T cell maintenance: molecular mediators of T cell differentiation and survivalR37AI067545 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Ananda W Goldrath · 2022 to 2026
$3.0M
IKK:Biophysical basis of dynamic regulationR01CA141722 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, GOURISANKAR, HOFFMANN, ALEXANDER · 2009 to 2013
$2.7M
Regulation of signaling via the lkB-NF-kB interactionR01GM071573 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HOFFMANN, ALEXANDER · 2005 to 2013
$2.2M
The NF-kB signaling system as a regulator of B-cell activationR01AI083453 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HOFFMANN, ALEXANDER · 2010 to 2014
$1.7M
NCI NIH HHS R01 CA141722NIAID NIH HHS R01 AI083453NIAID NIH HHS R37 AI067545NIGMS NIH HHS P50 GM085764NIGMS NIH HHS R01 GM071573
6 · The paper itself

Abstract

Targeted deletion of BAFF causes severe deficiency of splenic B cells. BAFF-R is commonly thought to signal to nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB)-inducing kinase dependent noncanonical NF-κB RelB. However, RelB-deficient mice have normal B-cell numbers. Recent studies showed that BAFF also signals to the canonical NF-κB pathway, and we found that both RelB and cRel are persistently activated, suggesting BAFF signaling coordinates both pathways to ensure robust B-cell development. Indeed, we report now that combined loss of these 2 NF-κB family members leads to impaired BAFF-mediated survival and development in vitro. Although single deletion of RelB and cRel was dispensable for normal B-cell development, double knockout mice displayed an early B-cell developmental blockade and decreased mature B cells. Despite disorganized splenic architecture in Relb(-/-)cRel(-/-) mice, generation of mixed-mouse chimeras established the developmental phenotype to be B-cell intrinsic. Together, our results indicate that BAFF signals coordinate both RelB and cRel activities to ensure survival during peripheral B-cell maturation.

Indexed as

AnimalsB-Cell Activating FactorB-Cell Activation Factor ReceptorB-LymphocytesCell SurvivalMiceMice, KnockoutProto-Oncogene Proteins c-retSignal TransductionTranscription Factor RelBB-Cell Activating FactorB-Cell Activation Factor ReceptorProto-Oncogene Proteins c-retRelb protein, mouseTnfrsf13c protein, mouseTnfsf13b protein, mouseTranscription Factor RelB

Identifiers

PMID26773039
PMCPMC4786837
OpenAlexW2292985931

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.