Evidence map›Paper›PMID 15270728›Full record

ArticleImmunology2004

Deficiency of BLNK hampers PLC-gamma2 phosphorylation and Ca2+ influx induced by the pre-B-cell receptor in human pre-B cells.

Tomoko Taguchi, Nobutaka Kiyokawa, Hisami Takenouch, Jun Matsui, Wei-Ran Tang, Hideki Nakajima, Kyoko Suzuki, Yusuke Shiozawa, Masahiro Saito, Yohko U Katagiri and 5 more

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. The Wheel of p53 Helps to Drive the Immune System.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Aberrant B-Cell Activation in Systemic Lupus Erythematosus.Kidney diseases (Basel, Switzerland) · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Regulation of Energy Metabolism during Early B Lymphocyte Development.International journal of molecular sciences · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Calcium signalling and cell-fate choice in B cells.Nature reviews. Immunology · 2007
    Review
  15. 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

15 authors at 5 institutions in 2 countries.

Tomoko TaguchiDepartment of Developmental Biology, National Research Institute for Child Health and Development, 3-35-31 Taishido, Setagaya-ku, Tokyo 154-8567, Japan.
Nobutaka Kiyokawa
Hisami Takenouch
Jun Matsui
Wei-Ran Tang
Hideki Nakajima
Kyoko Suzuki
Yusuke Shiozawa
Masahiro Saito
Yohko U Katagiri
Takao Takahashi
Hajime Karasuyama
Yoshinobu Matsuo
Hajime Okita
Junichiro Fujimoto
National Institutes of Health · USNational Center For Child Health and Development · JPKeio University · JPHayashibara (Japan) · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-cell linker protein (BLNK) is a component of the B-cell receptor (BCR) as well as of the pre-BCR signalling pathway, and BLNK(-/-) mice have a block in B lymphopoiesis at the pro-B/pre-B cell stage. A recent report described the complete loss or drastic reduction of BLNK expression in approximately 50% of human childhood pre-B acute lymphoblastic leukaemias (ALL), therefore we investigated BLNK expression in human pre-B ALL cell lines. One of the four cell lines tested, HPB-NULL cells, was found to lack BLNK expression, and we used these human pre-B ALL cell lines that express and do not express BLNK to investigate the intracellular signalling events following pre-BCR cross-linking. When pre-BCR was cross-linked with anti-micro heavy-chain antibodies, significant phosphorylation of intracellular molecules, including Syk, Shc, ERK MAP kinase, and AKT, and an activation of Ras were observed without regard to deficiency of BLNK expression, suggesting that BLNK is not required for pre-BCR-mediated activation of MAP kinase and phosphatidyl-inositol 3 (PI3) kinase signalling. By contrast, phospholipase C-gamma2 (PLC-gamma2) phosphorylation and an increase in intracellular Ca(2+) level mediated by pre-BCR cross-linking were observed only in the BLNK-expressing cells, indicating that BLNK is essential for PLC-gamma2-induced Ca(2+) influx. Human pre-B cell lines expressing and not expressing BLNK should provide an in vitro model for investigation of the role of BLNK in the pre-BCR-mediated signalling mechanism.

Indexed as

Adaptor Proteins, Signal TransducingB-LymphocytesCalciumCarrier ProteinsCell LineHumansMembrane GlycoproteinsPhospholipase C gammaPhosphoproteinsPhosphorylationPre-B Cell ReceptorsReceptors, Antigen, B-CellSignal TransductionType C PhospholipasesAdaptor Proteins, Signal TransducingB cell linker proteinCalciumCarrier ProteinsMembrane GlycoproteinsPhospholipase C gammaPhosphoproteinsPre-B Cell ReceptorsReceptors, Antigen, B-CellType C Phospholipases

Identifiers

PMID15270728
PMCPMC1782531
OpenAlexW2019600292

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.