Evidence map›Paper›PMID 18952291›Full record

ArticleMolecular immunology2009

B cell receptor crosstalk: B cells express osteopontin through the combined action of the alternate and classical BCR signaling pathways.

Benchang Guo, Joseph R Tumang, Thomas L Rothstein

Abstract read
In one paragraph

Article in Molecular immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 18 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

3 authors at 1 institution in 1 country.

Benchang GuoCenter for Oncology and Cell Biology, The Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY 11030, USA.
Joseph R Tumang
Thomas L Rothstein
Feinstein Institute for Medical Research · US

Funding

An Alternate Pathway to AutoimmunityR01AI075141 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI ROTHSTEIN, THOMAS L · 2008 to 2012
$1.8M
REGULATION OF FAS-MEDIATED APOPTOSIS IN B CELLSR01AI040181 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI ROTHSTEIN, THOMAS L · 1996 to 2006
$1.5M
Regulation of Fas-mediated ApoptosisR21AI040181 · NIAID · BOSTON MEDICAL CENTER · PI ROTHSTEIN, THOMAS L · 2001 to 2001
$280k
NIAID NIH HHS AI040181NIAID NIH HHS AI075141NIAID NIH HHS R01 AI040181NIAID NIH HHS R01 AI075141NIAID NIH HHS R21 AI040181
6 · The paper itself

Abstract

Classical BCR signaling requires a number of signalosome mediators that are bypassed when BCR signaling follows an alternate pathway produced by prior exposure of B cells to IL-4. The two pathways, classical and alternate, co-exist in IL-4-treated B cells. Here we report that operation of the IL-4-induced alternate pathway in combination with the classical pathway changes the nature of the B cell response to BCR engagement so that the cytokine, osteopontin (Opn), is produced and secreted. Although Opn expression by B cells has not previously been noted, anti-Ig-induced secretion by IL-4-treated B cells amounts to levels comparable to those secreted by activated T cells. However, unlike T cell Opn expression, B cell expression of Opn is not mediated by T-Bet. Because elevated levels of IL-4 occur in association with severe illness, and because Opn is strongly associated with autoimmunity, these results suggest that the IL-4-induced alternate BCR signaling pathway may participate in the pathophysiology of autoimmune dyscrasias.

Indexed as

AnimalsB-LymphocytesInterleukin-4MaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, Mutant StrainsOsteopontinReceptors, Antigen, B-CellSignal TransductionT-bet Transcription FactorT-Box Domain ProteinsInterleukin-4OsteopontinReceptors, Antigen, B-CellSpp1 protein, mouseT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID18952291
PMCPMC2631101
OpenAlexW2001165860

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.