Evidence map›Paper›PMID 19880579›Full record

ArticleInternational immunology2009

hnRNP-K is a nuclear target of TCR-activated ERK and required for T-cell late activation.

Jing-Wen Chang, Toru Koike, Makio Iwashima

Abstract read
In one paragraph

Article in International immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

3 authors.

Jing-Wen ChangDepartment of Medicine, Immunotherapy Center, Medical College of Georgia, Augusta, GA 30912-2600, USA.
Toru Koike
Makio Iwashima

Funding

THRESHOLD CONTROL FOR T CELL ANTIGEN RECEPTORR01AI047266 · NIAID · MEDICAL COLLEGE OF GEORGIA (MCG) · PI IWASHIMA, MAKIO · 2000 to 2004
$1.3M
Threshold control for T cell antigen receptorK02AI049398 · NIAID · MEDICAL COLLEGE OF GEORGIA (MCG) · PI IWASHIMA, MAKIO · 2001 to 2005
$543k
NIAID NIH HHS AI47266NIAID NIH HHS AI49398NIAID NIH HHS K02 AI049398NIAID NIH HHS R01 AI047266
6 · The paper itself

Abstract

Sustained extracellular signal-regulated kinase (ERK)-signaling plays a critical role in T-cell-mediated IL-2 production. Although many downstream targets are known for ERK, details remain unknown about which molecules play functional roles in IL-2 production. Here, we addressed this question using proteomic analysis of nuclear proteins from TCR-activated T cells and identified hnRNP-K as one of the ERK targets essential for IL-2 production. hnRNP-K was previously shown by others to be a direct substrate of ERK and form complexes with multiple signaling proteins as well as DNA and RNA. Our data showed a clear ERK-dependent increase in one form of hnRNP-K after TCR stimulation. Small interfering RNA-mediated gene knockdown of hnRNP-K expression abrogated IL-2 production by T cells. Moreover, reduction of hnRNP-K expression caused a notable increase in proteolysis of Vav1, a binding target of hnRNP-K. Since Vav1 is an essential molecule for T-cell activation, the data suggest that ERK signaling is required for T-cell activation partly by inhibiting activation-induced proteolysis of Vav1.

Indexed as

Lymphocyte ActivationAnimalsEnzyme ActivationExtracellular Signal-Regulated MAP KinasesHeterogeneous-Nuclear Ribonucleoprotein KHumansInterleukin-2Jurkat CellsMiceMice, Inbred BALB CProto-Oncogene Proteins c-vavReceptors, Antigen, T-CellSignal TransductionT-LymphocytesExtracellular Signal-Regulated MAP KinasesHeterogeneous-Nuclear Ribonucleoprotein KInterleukin-2Proto-Oncogene Proteins c-vavReceptors, Antigen, T-CellVAV1 protein, human

Identifiers

PMID19880579
PMCPMC2779832

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.