Evidence map›Paper›PMID 21976681›Full record

ArticleThe Journal of biological chemistry2011

Efnb1 and Efnb2 proteins regulate thymocyte development, peripheral T cell differentiation, and antiviral immune responses and are essential for interleukin-6 (IL-6) signaling.

Hongyu Luo, Tania Charpentier, Xuehai Wang, Shijie Qi, Bing Han, Tao Wu, Rafik Terra, Alain Lamarre, Jiangping Wu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
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  3. Proteomic Analysis of COVID-19 Infection.Advances in experimental medicine and biology · 2026
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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

9 authors at 3 institutions in 2 countries.

Hongyu LuoLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada.
Tania CharpentierInstitut National de la Recherche Scientifique, INRS-Institut Armand-Frappier, Laval, Québec H7V 1B7, Canada.
Xuehai WangLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada.
Shijie QiLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada.
Bing HanLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada.
Tao WuLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada; Institute of Cardiology, First Affiliated Hospital, Medical College, Zhejiang University, 310003 Hangzhou, China.
Rafik TerraLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada.
Alain LamarreInstitut National de la Recherche Scientifique, INRS-Institut Armand-Frappier, Laval, Québec H7V 1B7, Canada.
Jiangping WuLaboratoire Immunologie, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada; Service Nephrologie, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Notre-Dame Hospital, Montreal, Quebec H2L 4M1, Canada. Electronic address: jianping.wu@umontreal.ca.
Hôpital Notre-Dame · CAInstitut National de la Recherche Scientifique · CAFirst Affiliated Hospital Zhejiang University · CN

Funding

Canadian Institutes of Health Research IMH 79565Canadian Institutes of Health Research MOP57697Canadian Institutes of Health Research MOP69089Canadian Institutes of Health Research MOP89797Canadian Institutes of Health Research MOP97829
6 · The paper itself

Abstract

Erythropoietin-producing hepatocellular kinases (Eph kinases) constitute the largest family of cell membrane receptor tyrosine kinases, and their ligand ephrins are also cell surface molecules. Because of promiscuous interaction between Ephs and ephrins, there is considerable redundancy in this system, reflecting the essential roles of these molecules in the biological system through evolution. In this study, both Efnb1 and Efnb2 were null-mutated in the T cell compartment of mice through loxP-mediated gene deletion. Mice with this double conditional mutation (double KO mice) showed reduced thymus and spleen size and cellularity. There was a significant decrease in the DN4, double positive, and single positive thymocyte subpopulations and mature CD4 and CD8 cells in the periphery. dKO thymocytes and peripheral T cells failed to compete with their WT counterparts in irradiated recipients, and the T cells showed compromised ability of homeostatic expansion. dKO naive T cells were inferior in differentiating into Th1 and Th17 effectors in vitro. The dKO mice showed diminished immune response against LCMV infection. Mechanistic studies revealed that IL-6 signaling in dKO T cells was compromised, in terms of abated induction of STAT3 phosphorylation upon IL-6 stimulation. This defect likely contributed to the observed in vitro and in vivo phenotype in dKO mice. This study revealed novel roles of Efnb1 and Efnb2 in T cell development and function.

Indexed as

Immunity, InnateAnimalsCD8-Positive T-LymphocytesCell DifferentiationEphrin-B1Interleukin-6Lymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, KnockoutOrgan SizePhosphorylationSignal TransductionSpleenSTAT3 Transcription FactorTh17 CellsEfnb1 protein, mouseEphrin-B1Interleukin-6Stat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID21976681
PMCPMC3308828
OpenAlexW2070371849

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.