Evidence map›Paper›PMID 27183586›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

NKAP Regulates Invariant NKT Cell Proliferation and Differentiation into ROR-γt-Expressing NKT17 Cells.

Puspa Thapa, Meibo W Chen, Douglas C McWilliams, Paul Belmonte, Megan Constans, Derek B Sant'Angelo, Virginia Smith Shapiro

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Markers and makers of NKT17 cells.Experimental & molecular medicine · 2023
    Review
  7. Article
  8. Review
  9. Recent Update of HDAC Inhibitors in Lymphoma.Frontiers in cell and developmental biology · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. NKAP alters tumor immune microenvironment and promotes glioma growth via Notch1 signaling.Journal of experimental & clinical cancer research : CR · 2019
    Article
  14. Article
  15. Article
  16. Review
  17. Differential Control ofFrontiers in immunology · 2019
    Article
  18. Article
  19. Article
  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

7 authors at 2 institutions in 1 country.

Puspa ThapaDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Meibo W ChenDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Douglas C McWilliamsDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Paul BelmonteDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Megan ConstansDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and.
Derek B Sant'AngeloDepartment of Pediatrics, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ 08901.ORCID 0000-0002-5510-9367
Virginia Smith ShapiroDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; and Shapiro.virginia1@mayo.edu.
Mayo Clinic in Arizona · USRutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
The Role for NKAP in iNKT cell developmentR21AI093944 · NIAID · MAYO CLINIC ROCHESTER · PI SHAPIRO, VIRGINIA SMITH · 2011 to 2012
$434k
NCI NIH HHS P30 CA072720NIAID NIH HHS HHSN272201300006CNIAID NIH HHS R21 AI093944
6 · The paper itself

Abstract

Invariant NKT (iNKT) cells are a unique lineage with characteristics of both adaptive and innate lymphocytes, and they recognize glycolipids presented by an MHC class I-like CD1d molecule. During thymic development, iNKT cells also differentiate into NKT1, NKT2, and NKT17 functional subsets that preferentially produce cytokines IFN-γ, IL-4, and IL-17, respectively, upon activation. Newly selected iNKT cells undergo a burst of proliferation, which is defective in mice with a specific deletion of NKAP in the iNKT cell lineage, leading to severe reductions in thymic and peripheral iNKT cell numbers. The decreased cell number is not due to defective homeostasis or increased apoptosis, and it is not rescued by Bcl-xL overexpression. NKAP is also required for differentiation into NKT17 cells, but NKT1 and NKT2 cell development and function are unaffected. This failure in NKT17 development is rescued by transgenic expression of promyelocytic leukemia zinc finger; however, the promyelocytic leukemia zinc finger transgene does not restore iNKT cell numbers or the block in positive selection into the iNKT cell lineage in CD4-cre NKAP conditional knockout mice. Therefore, NKAP regulates multiple steps in iNKT cell development and differentiation.

Indexed as

Cell DifferentiationGene Expression RegulationAnimalsbcl-X ProteinCell ProliferationCytokinesInterleukin-17Interleukin-4Lymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsNuclear Receptor Subfamily 1, Group F, Member 3Repressor ProteinsBcl2l1 protein, mousebcl-X ProteinCytokinesInterleukin-17Interleukin-4NKAP protein, mouseNuclear Receptor Subfamily 1, Group F, Member 3Repressor Proteins

Identifiers

PMID27183586
PMCPMC4893932
OpenAlexW2345584371

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.