Evidence map›Paper›PMID 15792999›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Commitment toward the natural T (iNKT) cell lineage occurs at the CD4+8+ stage of thymic ontogeny.

Jelena S Bezbradica, Timothy Hill, Aleksandar K Stanic, Luc Van Kaer, Sebastian Joyce

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing 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

66 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Markers and makers of NKT17 cells.Experimental & molecular medicine · 2023
    Review
  5. E protein binding at theFrontiers in immunology · 2023
    Article
  6. Article
  7. Article
  8. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  9. Article
  10. Review
  11. Review
  12. Nur77 controls tolerance induction, terminal differentiation, and effector functions in semi-invariant natural killer T cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Sumoylation of RORγt regulates TNature communications · 2018
    Article

6 more citing papers are in PubMed but not listed here.

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.

Jelena S BezbradicaDepartment of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Timothy Hill
Aleksandar K Stanic
Luc Van Kaer
Sebastian Joyce

Funding

T Lymphocyte based functional genomics of inflammationP01HL068744 · NHLBI · VANDERBILT UNIVERSITY · PI MOORE, JASON H. · 2002 to 2006
$9.9M
MOLECULAR BASIS OF CDLDL AND NATURAL T CELL FUNCTIONR01AI042284 · NIAID · VANDERBILT UNIVERSITY · PI JOYCE, SEBASTIAN · 1998 to 2013
$3.1M
Modulation of type I diabetes with NKT cellsR01AI050953 · NIAID · VANDERBILT UNIVERSITY · PI VAN KAER, LUC · 2002 to 2006
$1.8M
Modulation of EAE with ligand-activated NKT cellsR01NS044044 · NINDS · VANDERBILT UNIVERSITY · PI VAN KAER, LUC · 2002 to 2005
$1.3M
Transcriptional Regulation of the Type 1 T Cell ResponseR01AI049460 · NIAID · VANDERBILT UNIVERSITY · PI BOOTHBY, MARK R. · 2002 to 2005
$1.3M
Transciptional Regulation of the Type 1 T Cell ResponseR21AI049460 · NIAID · VANDERBILT UNIVERSITY · PI BOOTHBY, MARK R. · 2001 to 2001
$338k
Molecular Basis of CD1d1 and Natural T Cell FunctionR21AI042284 · NIAID · VANDERBILT UNIVERSITY · PI JOYCE, SEBASTIAN · 2002 to 2002
$302k
NHLBI NIH HHS HL068744NHLBI NIH HHS P01 HL068744NIAID NIH HHS AI042284NIAID NIH HHS AI050953NIAID NIH HHS AI49460NIAID NIH HHS R01 AI042284NIAID NIH HHS R01 AI049460NIAID NIH HHS R01 AI050953NIAID NIH HHS R21 AI042284NIAID NIH HHS R21 AI049460NINDS NIH HHS NS044044NINDS NIH HHS R01 NS044044
6 · The paper itself

Abstract

T lineage commitment occurs in a discrete, stage-specific manner during thymic ontogeny. Intrathymic precursor transfer experiments and the identification of CD4(+)8+ double-positive (DP), V alpha 14J alpha 18 natural T (iNKT) cells suggest that commitment to this lineage might occur at the DP stage. Nevertheless, this matter remains contentious because others failed to detect V alpha 14J alpha 18-positive iNKT cells that are CD4(+)8+. In resolution to this issue, we demonstrate that retinoic acid receptor-related orphan receptor gamma (ROR gamma)0/0 thymi, which accumulate immature single-positive (ISP) thymocytes that precede the DP stage, do not rearrange V alpha 14-to-J alpha 18 gene segments, suggesting that this event occurs at a post-ISP stage. Mixed radiation bone marrow chimeras revealed that RORgamma functions in an iNKT cell lineage-specific manner. Further, introgression of a Bcl-x(L) transgene into ROR gamma(0/0) mice, which promotes survival and permits secondary rearrangements of distal V alpha and J alpha gene segments at the DP stage, rescues V alpha 14-to-J alpha 18 recombination. Similarly, introgression of a rearranged V alpha 14J alpha 18 transgene into ROR gamma(0/0) mice results in functional iNKT cells. Thus, our data support the "T cell receptor-instructive (mainstream precursor) model" of iNKT cell lineage specification where V alpha 14-to-J alpha 18 rearrangement, positive selection, and iNKT cell lineage commitment occur at or after the DP stage of ontogeny.

Indexed as

AnimalsBase SequenceCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationDNA, ComplementaryGene Rearrangement, T-LymphocyteImmunity, InnateKiller Cells, NaturalLymphopoiesisMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicModels, ImmunologicalNuclear Receptor Subfamily 1, Group F, Member 3DNA, ComplementaryNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Retinoic AcidReceptors, Thyroid HormoneRorc protein, mouse

Identifiers

PMID15792999
PMCPMC555981

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.