Evidence map›Paper›PMID 19952372›Full record

ArticleScience signaling2009

RIAM regulates the cytoskeletal distribution and activation of PLC-gamma1 in T cells.

Nikolaos Patsoukis, Esther M Lafuente, Paul Meraner, Jin sub Kim, David Dombkowski, Lequn Li, Vassiliki A Boussiotis

Abstract read
In one paragraph

Article in Science signaling, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Expression of the phagocytic receptors αFrontiers in immunology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Molecular basis for autoinhibition of RIAM regulated by FAK in integrin activation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  14. Article
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  16. Article
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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

7 authors at 2 institutions in 1 country.

Nikolaos PatsoukisDepartment of Hematology-Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Center for Life Sciences, Harvard Medical School, Boston, MA 02215, USA.
Esther M Lafuente
Paul Meraner
Jin sub Kim
David Dombkowski
Lequn Li
Vassiliki A Boussiotis
Harvard University · USMassachusetts General Hospital · US

Funding

The Role of Rap1 in T-Cell ResponsesR01AI043552 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI BOUSSIOTIS, VASSILIKI A · 1998 to 2009
$2.1M
Expression and Function of Tob in T LymphocytesR01CA104596 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BOUSSIOTIS, VASSILIKI A · 2005 to 2009
$1.6M
Reconstitution of T cell immunity after UCB transplantation: The role of TregR21CA123855 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2008 to 2009
$783k
NCI NIH HHS R01 CA104596NCI NIH HHS R21 CA123855NIAID NIH HHS R01 AI043552
6 · The paper itself

Abstract

Rap1-guanosine triphosphate (GTP)-interacting adaptor molecule (RIAM) plays a critical role in actin reorganization and inside-out activation of integrins in lymphocytes and platelets. We investigated the role of RIAM in T cell receptor (TCR)-mediated signaling. Although phosphorylation of the kinase ZAP-70 and formation of a signalosome recruited to the adaptor protein LAT were unaffected, elimination of endogenous RIAM by short hairpin RNA impaired generation of inositol 1,4,5-trisphosphate, mobilization of intracellular calcium ions (Ca(2+)), and translocation of the transcription factor NFAT to the nucleus. The activation of Ras guanine nucleotide-releasing protein 1 was also impaired, which led to the diminished expression of the gene encoding interleukin-2. These events were associated with the impaired translocation of phosphorylated phospholipase C-gamma1 (PLC-gamma1) to the actin cytoskeleton, which was required to bring PLC-gamma1 close to its substrate phosphatidylinositol 4,5-bisphosphate, and were reversed by reconstitution of cells with RIAM. Thus, by regulating the localization of PLC-gamma1, RIAM plays a central role in TCR signaling and the transcription of target genes.

Indexed as

Adaptor Proteins, Signal TransducingCells, CulturedCytoskeletonHumansJurkat CellsMembrane ProteinsPhosphatidylinositol 4,5-DiphosphatePhosphatidylinositol PhosphatesPhospholipase C gammaProtein TransportReceptors, Antigen, T-CellSignal TransductionTranscription, GeneticAdaptor Proteins, Signal TransducingAPBB1IP protein, humanMembrane ProteinsPhosphatidylinositol 4,5-DiphosphatePhosphatidylinositol PhosphatesPhospholipase C gammaReceptors, Antigen, T-Cell

Identifiers

PMID19952372
PMCPMC2908902
OpenAlexW2159641065

What OpenQuestion holds

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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.