Evidence map›Paper›PMID 28724935›Full record

ArticleScientific reports2017

Histone deacetylase 3 is required for iNKT cell development.

Puspa Thapa, Sinibaldo Romero Arocha, Ji Young Chung, Derek B Sant'Angelo, Virginia Smith Shapiro

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Role of Histone Deacetylases in T-Cell Development and Function.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Review
  6. Genetic Analysis of iNKT Cell Development and Function.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Recent Update of HDAC Inhibitors in Lymphoma.Frontiers in cell and developmental biology · 2020
    Review
  11. Review
  12. Article
  13. Article
  14. CD24Immune network · 2019
    Article
  15. Article
  16. Differential Control ofFrontiers in immunology · 2019
    Article
  17. Review
  18. Article
  19. Histone deacetylase function in CD4Nature reviews. Immunology · 2018
    Review
  20. Review
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

5 authors.

Puspa ThapaDepartment of Immunology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Sinibaldo Romero ArochaDepartment of Immunology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Ji Young ChungDepartment of Immunology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Derek B Sant'AngeloDepartment of Pediatrics, Rutgers Robert Wood Johnson Medical School and The Children's Health Institute of New Jersey, 89 French Street, Room 4273, New Brunswick, NJ, 08901, USA.
Virginia Smith ShapiroDepartment of Immunology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA. shapiro.virginia1@mayo.edu.

Funding

Regulation of T cell maturationR01AI083279 · NIAID · MAYO CLINIC ROCHESTER · PI SHAPIRO, VIRGINIA SMITH · 2010 to 2019
$3.8M
The Role for NKAP in iNKT cell developmentR21AI093944 · NIAID · MAYO CLINIC ROCHESTER · PI SHAPIRO, VIRGINIA SMITH · 2011 to 2012
$434k
NIAID NIH HHS R01 AI083279NIAID NIH HHS R21 AI093944
6 · The paper itself

Abstract

NKT cells are a distinct subset that have developmental requirements that often differ from conventional T cells. Here, we show that NKT-specific deletion of Hdac3 results in a severe reduction in the number of iNKT cells, particularly of NKT1 cells. In addition, there is decreased cytokine production by Hdac3-deficient NKT2 and NKT17 cells. Hdac3-deficient iNKT cells have increased cell death that is not rescued by transgenic expression of Bcl-2 or Bcl-xL. Hdac3-deficient iNKT cells have less Cyto-ID staining and lower LC3A/B expression, indicative of reduced autophagy. Interestingly, Hdac3-deficient iNKT cells also have lower expression of the nutrient receptors GLUT1, CD71 and CD98, which would increase the need for autophagy when nutrients are limiting. Therefore, Hdac3 is required for iNKT cell development and differentiation.

Indexed as

Cell DifferentiationAnimalsApoptosisCell SurvivalCytokinesGene DeletionHistone Deacetylase 3Histone DeacetylasesMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsCytokinesHistone Deacetylase 3Histone Deacetylases

Identifiers

PMID28724935
PMCPMC5517478

What OpenQuestion holds

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Registered trials

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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.