Evidence map›Paper›PMID 8943371›Full record

ArticleMolecular and cellular biology1996

The kinase, SH3, and SH2 domains of Lck play critical roles in T-cell activation after ZAP-70 membrane localization.

S Yamasaki, M Takamatsu, M Iwashima

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 40 citations in OpenAlex.

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  6. T-cell receptor signaling is mediated by transient Lck activity, which is inhibited by inorganic mercury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009
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  8. Genetic evidence for Shc requirement in TCR-induced c-Rel nuclear translocation and IL-2 expression.Proceedings of the National Academy of Sciences of the United States of America · 2002
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  10. Review
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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 2 institutions in 2 countries.

S YamasakiDivision of Cell and Information, Precursory Research for Embryonic Science and Technology, Research Development Corporation of Japan, Tokyo.
M Takamatsu
M Iwashima
ARCH Development Corporation · USMitsubishi Group (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigenic stimulation of the T-cell antigen receptor initiates signal transduction through the immunoreceptor tyrosine-based activation motifs (ITAMs). When its two tyrosines are phosphorylated, ITAM forms a binding site for ZAP-70, one of the cytoplasmic protein tyrosine kinases essential for T-cell activation. The signaling process that follows ZAP-70 binding to ITAM has been analyzed by the construction of fusion proteins that localize ZAP-70 to the plasma membrane. We found that membrane-localized forms of ZAP-70 induce late signaling events such as activation of nuclear factor of activated T cells without any stimulation. This activity was observed only when Lck was expressed and functional. In addition, each mutation that affects the function of Lck in the kinase, Src homology 2 (SH2), and SH3 domains greatly impaired the signaling ability of the chimeric protein. Therefore, Lck functions in multiple manners in T-cell activation for the steps following ZAP-70 binding to ITAM.

Indexed as

Signal TransductionHumansJurkat CellsLymphocyte ActivationLymphocyte Specific Protein Tyrosine Kinase p56(lck)Protein-Tyrosine KinasesReceptors, Antigen, T-Cellsrc-Family Kinasessrc Homology DomainsT-LymphocytesZAP-70 Protein-Tyrosine KinaseLymphocyte Specific Protein Tyrosine Kinase p56(lck)Protein-Tyrosine KinasesReceptors, Antigen, T-Cellsrc-Family KinasesZAP70 protein, humanZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID8943371
PMCPMC231719
OpenAlexW2131150636

What OpenQuestion holds

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Registered trials

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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.