Evidence map›Paper›PMID 23509253›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

FCRL5 exerts binary and compartment-specific influence on innate-like B-cell receptor signaling.

Zilu Zhu, Ran Li, Hao Li, Tong Zhou, Randall S Davis

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Curcumin alleviates experimental colitisWorld journal of gastroenterology · 2022
    Article
  10. Article
  11. FCRL1 Regulates B Cell Receptor-Induced ERK Activation through GRB2.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  12. Age-associated B Cells Appear in Patients with Granulomatous Lung Diseases.American journal of respiratory and critical care medicine · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. FCRL5Cell reports · 2019
    Article
  17. eLife · 2018
    Article
  18. FCRL regulation in innate-like B cells.Annals of the New York Academy of Sciences · 2015
    Review
  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

5 authors at 2 institutions in 2 countries.

Zilu ZhuDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Ran Li
Hao Li
Tong Zhou
Randall S Davis
University of Alabama at Birmingham · USCzech Academy of Sciences, Institute of Microbiology · CZ

Funding

Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
Functional Role of Fc Receptor Homologs on B Lineage CellsR01AI067467 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVIS, RANDALL S · 2007 to 2011
$1.6M
NIAID NIH HHS AI027767NIAID NIH HHS AI067467NIAID NIH HHS P30 AI027767NIAID NIH HHS R01 AI067467NIAMS NIH HHS P30 AR048311NIAMS NIH HHS P30 AR48311
6 · The paper itself

Abstract

Innate-like splenic marginal zone (MZ) and peritoneal cavity B1 B lymphocytes share critical responsibilities in humoral responses but have divergent B-cell receptor (BCR) signaling features. A discrete marker of these subsets with tyrosine-based dual regulatory potential termed "Fc receptor-like 5" (FCRL5) was investigated to explore this discrepancy. Although FCRL5 repressed the robust BCR activity that is characteristic of MZ B cells, it had no influence on antigen receptor stimulation that is blunted in peritoneal cavity-derived B1 B cells. The molecular basis for the receptor's inhibitory function derived from recruitment of the Src homology-2 domain-containing tyrosine phosphatase 1 (SHP-1) to a cytoplasmic immunoreceptor tyrosine-based inhibitory motif. Surprisingly, mutagenesis of this docking site unearthed coactivation properties for FCRL5 that were orchestrated by independent association of the Lyn Src-family kinase with an intracellular immunoreceptor tyrosine-based activation motif-like sequence. FCRL5's unique binary regulation directly correlated with SHP-1 and Lyn activity, which, like BCR function, differed between MZ and B1 B cells. These findings collectively imply a specialized counterregulatory role for FCRL molecules at the intersection of innate and adaptive immunity.

Indexed as

AnimalsB-Cell Activating FactorCalciumCell LineDNA PrimersImmunity, InnateImmunoblottingMiceMicroscopy, ConfocalReceptors, Antigen, B-CellReceptors, FcSignal TransductionSpleenB-Cell Activating FactorCalciumDNA PrimersFcRH3 protein, mouseReceptors, Antigen, B-CellReceptors, FcTNFSF13B protein, human

Identifiers

PMID23509253
PMCPMC3619311
OpenAlexW2136985023

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.