Evidence map›Paper›PMID 12070286›Full record

ArticleThe Journal of experimental medicine2002

Constitutive endocytosis and degradation of the pre-T cell receptor.

Maddalena Panigada, Simona Porcellini, Eliane Barbier, Sonja Hoeflinger, Pierre-André Cazenave, Hua Gu, Hamid Band, Harald von Boehmer, Fabio Grassi

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. The Function of Ubiquitination in T-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  2. Ubiquitination of Immune System and Cancer Therapy.Advances in experimental medicine and biology · 2024
    Review
  3. Review
  4. Article
  5. Notch Partners in the Long Journey of T-ALL Pathogenesis.International journal of molecular sciences · 2023
    Review
  6. Genetically modified hematopoietic stem/progenitor cells that produce IL-10-secreting regulatory T cells.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  7. Article
  8. Article
  9. Transcription factors and target genes of pre-TCR signaling.Cellular and molecular life sciences : CMLS · 2015
    Review
  10. Enforcement of γδ-lineage commitment by the pre-T-cell receptor in precursors with weak γδ-TCR signals.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

9 authors.

Maddalena PanigadaDipartimento di Biologia e Genetica per le Scienze Mediche, Università degli Studi di Milano, Italy.
Simona Porcellini
Eliane Barbier
Sonja Hoeflinger
Pierre-André Cazenave
Hua Gu
Hamid Band
Harald von Boehmer
Fabio Grassi

Funding

IN VIVO ANALYSIS OF INTRACELLULAR SIGNALS CONTROLLING LYMPHOCYTEZ01AI000719 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI GU, HUA · 1995 to 2002
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6 · The paper itself

Abstract

The pre-T cell receptor (TCR) signals constitutively in the absence of putative ligands on thymic stroma and signal transduction correlates with translocation of the pre-TCR into glycolipid-enriched microdomains (rafts) in the plasma membrane. Here, we show that the pre-TCR is constitutively routed to lysosomes after reaching the cell surface. The cell-autonomous down-regulation of the pre-TCR requires activation of the src-like kinase p56(lck), actin polymerization, and dynamin. Constitutive signaling and degradation represents a feature of the pre-TCR because the gammadeltaTCR expressed in the same cell line does not exhibit these features. This is also evident by the observation that the protein adaptor/ubiquitin ligase c-Cbl is phosphorylated and selectively translocated into rafts in pre-TCR- but not gammadeltaTCR-expressing cells. A role of c-Cbl-mediated ubiquitination in pre-TCR degradation is supported by the reduction of degradation through pharmacological inhibition of the proteasome and through a dominant-negative c-Cbl ubiquitin ligase as well as by increased pre-TCR surface expression on immature thymocytes in c-Cbl-deficient mice. The pre-TCR internalization contributes significantly to the low surface level of the receptor on developing T cells, and may in fact be a requirement for optimal pre-TCR function.

Indexed as

EndocytosisActinsAnimalsBiopolymersCell MembraneCysteine EndopeptidasesDynaminsGTP PhosphohydrolasesHydrolysisLymphocyte Specific Protein Tyrosine Kinase p56(lck)LysosomesMiceMice, SCIDMultienzyme ComplexesProteasome Endopeptidase ComplexReceptors, Antigen, T-CellActinsBiopolymersCysteine EndopeptidasesDynaminsGTP PhosphohydrolasesLymphocyte Specific Protein Tyrosine Kinase p56(lck)Multienzyme ComplexesProteasome Endopeptidase ComplexReceptors, Antigen, T-Cell

Identifiers

PMID12070286
PMCPMC2193560

What OpenQuestion holds

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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.