Evidence map›Paper›PMID 28553951›Full record

ArticleNature immunology2017

Post-translational control of T cell development by the ESCRT protein CHMP5.

Stanley Adoro, Kwang Hwan Park, Sarah E Bettigole, Raphael Lis, Hee Rae Shin, Heewon Seo, Ju Han Kim, Klaus-Peter Knobeloch, Jae-Hyuck Shim, Laurie H Glimcher

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. USP8-Governed MDA5 Homeostasis Promotes Innate Immunity and Autoimmunity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Deubiquitinases and Cancer.Journal of pharmacy & bioallied sciences · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. The Function of Ubiquitination in T-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  13. Article
  14. Article
  15. Bro1 family proteins harmonize cargo sorting with vesicle formation.BioEssays : news and reviews in molecular, cellular and developmental biology · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Protein ubiquitination in T cell development.Frontiers in immunology · 2022
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Stanley AdoroDepartment of Cancer Immunology and Virology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Kwang Hwan ParkDepartment of Pathology, Weill Cornell Medicine, New York, New York, USA.
Sarah E BettigoleQuentis Therapeutics, New York, New York, USA.
Raphael LisAnsary Stem Cell Institute, Department of Genetic Medicine, Weill Cornell Medicine, New York, New York, USA.
Hee Rae ShinQuentis Therapeutics, New York, New York, USA.
Heewon SeoDivision of Biomedical Informatics, Seoul National University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0001-6218-8609
Ju Han KimDivision of Biomedical Informatics, Seoul National University College of Medicine, Seoul, South Korea.
Klaus-Peter KnobelochInstitute for Neuropathology, University of Freiburg, Freiburg, Germany.
Jae-Hyuck ShimDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Laurie H GlimcherDepartment of Cancer Immunology and Virology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Cornell University · USHarvard University · USSeoul National University · KRUniversity of Freiburg · DEUniversity of Massachusetts Chan Medical School · US

Funding

Identification of novel regulators governing osteoclast-osteoblast couplingR01AR068983 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHIM, JAE-HYUCK · 2016 to 2020
$1.9M
6 · The paper itself

Abstract

The acquisition of a protective vertebrate immune system hinges on the efficient generation of a diverse but self-tolerant repertoire of T cells by the thymus through mechanisms that remain incompletely resolved. Here we identified the endosomal-sorting-complex-required-for-transport (ESCRT) protein CHMP5, known to be required for the formation of multivesicular bodies, as a key sensor of thresholds for signaling via the T cell antigen receptor (TCR) that was essential for T cell development. CHMP5 enabled positive selection by promoting post-selection thymocyte survival in part through stabilization of the pro-survival protein Bcl-2. Accordingly, loss of CHMP5 in thymocyte precursor cells abolished T cell development, a phenotype that was 'rescued' by genetic deletion of the pro-apoptotic protein Bim or transgenic expression of Bcl-2. Mechanistically, positive selection resulted in the stabilization of CHMP5 by inducing its interaction with the deubiquitinase USP8. Our results thus identify CHMP5 as an essential component of the post-translational machinery required for T cell development.

Indexed as

AnimalsBcl-2-Like Protein 11Cell DifferentiationEndopeptidasesEndosomal Sorting Complexes Required for TransportImmunoblottingImmunoprecipitationMiceMicroscopy, Electron, TransmissionMicroscopy, FluorescenceProtein Processing, Post-TranslationalProto-Oncogene Proteins c-bcl-2Real-Time Polymerase Chain ReactionReceptors, Antigen, T-CellSignal TransductionThymocytesBcl2l11 protein, mouseBcl-2-Like Protein 11Bcl2 protein, mouseCHMP5 protein, mouseEndopeptidasesEndosomal Sorting Complexes Required for TransportProto-Oncogene Proteins c-bcl-2Receptors, Antigen, T-CellUbiquitin ThiolesteraseUsp8 protein, mouse

Identifiers

PMID28553951
OpenAlexW2618746729

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.