Evidence map›Paper›PMID 26869226›Full record

ArticleJournal of cell science2016

HDAC6 regulates the dynamics of lytic granules in cytotoxic T lymphocytes.

Norman Núñez-Andrade, Salvador Iborra, Antonio Trullo, Olga Moreno-Gonzalo, Enrique Calvo, Elena Catalán, Gaël Menasche, David Sancho, Jesús Vázquez, Tso-Pang Yao and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2016. 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
2.8field-weighted citation impact, top 10% 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, 42 citations in OpenAlex.

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  12. Extracellular vesicles fromFrontiers in immunology · 2022
    Article
  13. Folding for the Immune Synapse: CCT Chaperonin and the Cytoskeleton.Frontiers in cell and developmental biology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
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  19. Article
  20. Aurora A controls CD8Scientific reports · 2019
    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

12 authors at 7 institutions in 4 countries.

Norman Núñez-AndradeServicio de Inmunología, Hospital Universitario de la Princesa, UAM, IIS-IP. Madrid, 28006 Spain.
Salvador IborraImmunobiology of inflammation, Fundación CNIC, Madrid, 28029 Spain.
Antonio TrulloMicroscopy and Dynamic Imaging Unit, Fundación CNIC, Madrid, 28029 Spain.
Olga Moreno-GonzaloServicio de Inmunología, Hospital Universitario de la Princesa, UAM, IIS-IP. Madrid, 28006 Spain.
Enrique CalvoProteomic Unit. Fundación CNIC, Madrid, 28029 Spain.
Elena CatalánDept. Biochemistry and Molecular and Cell Biology, Universidad de Zaragoza, 500009, Spain.
Gaël MenascheLaboratory of Normal and Pathological Homeostasis of the Immune System, INSERM Unité Mixte de Recherche 1163, Paris France.
David SanchoImmunobiology of inflammation, Fundación CNIC, Madrid, 28029 Spain.
Jesús VázquezProteomic Unit. Fundación CNIC, Madrid, 28029 Spain.
Tso-Pang YaoDepartments of Pharmacology and Cancer Biology Duke University, Medical Center, Durham, North Carolina 27710, U.S.
Noa Beatriz Martín-Cófreces *Servicio de Inmunología, Hospital Universitario de la Princesa, UAM, IIS-IP. Madrid, 28006 Spain.
Francisco Sánchez-Madrid *Servicio de Inmunología, Hospital Universitario de la Princesa, UAM, IIS-IP. Madrid, 28006 Spain.
Hospital Universitario de La Princesa · ESFundación Pro CNIC · ESDuke Medical Center · USInserm · FRIRCCS Ospedale San Raffaele · ITUniversidad Autónoma de Madrid · ESUniversidad de Zaragoza · ES

Funding

European Research Council 294340
6 · The paper itself

Abstract

HDAC6 is a tubulin deacetylase involved in many cellular functions related to cytoskeleton dynamics, including cell migration and autophagy. In addition, HDAC6 affects antigen-dependent CD4(+)T cell activation. In this study, we show that HDAC6 contributes to the cytotoxic function of CD8(+)T cells. Immunization studies revealed defective cytotoxic activity in vivo in the absence of HDAC6. Adoptive transfer of wild-type or Hdac6(-/-)CD8(+)T cells to Rag1(-/-)mice demonstrated specific impairment in CD8(+)T cell responses against vaccinia infection. Mechanistically, HDAC6-deficient cytotoxic T lymphocytes (CTLs) showed defective in vitro cytolytic activity related to altered dynamics of lytic granules, inhibited kinesin-1-dynactin-mediated terminal transport of lytic granules to the immune synapse and deficient exocytosis, but not to target cell recognition, T cell receptor (TCR) activation or interferon (IFN)γ production. Our results establish HDAC6 as an effector of the immune cytotoxic response that acts by affecting the dynamics, transport and secretion of lytic granules by CTLs.

Indexed as

AnimalsBiological TransportCells, CulturedCytoplasmic GranulesCytotoxicity, ImmunologicDynactin ComplexHistone Deacetylase 6Histone DeacetylasesInterferon-gammaKinesinsMiceMice, Inbred C57BLMice, KnockoutT-Lymphocytes, CytotoxicVacciniaDynactin ComplexHdac6 protein, mouseHistone Deacetylase 6Histone DeacetylasesInterferon-gammaKif5b protein, mouseKinesinsHistone deacetylase 6Kinesin 1Lytic granule

Identifiers

PMID26869226
PMCPMC5023047
OpenAlexW2255543900

What OpenQuestion holds

Textmetadata
LicenceTDM
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.