Evidence map›Paper›PMID 19561613›Full record

ArticleNature immunology2009

Essential function for the GTPase TC21 in homeostatic antigen receptor signaling.

Pilar Delgado, Beatriz Cubelos, Enrique Calleja, Nuria Martínez-Martín, Angel Ciprés, Isabel Mérida, Carmen Bellas, Xosé R Bustelo, Balbino Alarcón

Abstract read
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In one paragraph

Article in Nature immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

65 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The ancestral type of the R-RAS protein has oncogenic potential.Cellular & molecular biology letters · 2024
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  12. The RASopathies: from pathogenetics to therapeutics.Disease models & mechanisms · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Observational
  18. Active GTPase Pulldown Protocol.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  19. Article
  20. Article

5 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 1 country.

Pilar DelgadoCentro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, Cantoblanco, Spain.
Beatriz Cubelos
Enrique Calleja
Nuria Martínez-Martín
Angel Ciprés
Isabel Mérida
Carmen Bellas
Xosé R Bustelo
Balbino Alarcón
Centro Nacional de Biotecnología · ESConsejo Superior de Investigaciones Científicas · ESHospital Universitario Puerta de Hierro Majadahonda · ESUniversidad Autónoma de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell antigen receptors (TCRs) and B cell antigen receptors (BCRs) transmit low-grade signals necessary for the survival and maintenance of mature cell pools. We show here that TC21, a small GTPase encoded by Rras2, interacted constitutively with both kinds of receptors. Expression of a dominant negative TC21 mutant in T cells produced a rapid decrease in cell viability, and Rras2(-/-) mice were lymphopenic, possibly as a result of diminished homeostatic proliferation and impaired T cell and B cell survival. In contrast, TC21 was overexpressed in several human lymphoid malignancies. Finally, the p110delta catalytic subunit of phosphatidylinositol-3-OH kinase (PI(3)K) was recruited to the TCR and BCR in a TC21-dependent way. Consequently, we propose TC21 directly links antigen receptors to PI(3)K-mediated survival pathways.

Indexed as

AnimalsB-LymphocytesCell SurvivalHomeostasisHumansLymph NodesLymphoma, B-CellLymphoma, T-CellMembrane ProteinsMiceMonomeric GTP-Binding ProteinsPhosphatidylinositol 3-KinasesReceptors, Antigen, B-CellReceptors, Antigen, T-CellSignal TransductionT-LymphocytesMembrane ProteinsMonomeric GTP-Binding ProteinsPhosphatidylinositol 3-KinasesReceptors, Antigen, B-CellReceptors, Antigen, T-CellRRAS2 protein, humanRras2 protein, mouse

Identifiers

PMID19561613
OpenAlexW2018099136

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.