Evidence map›Paper›PMID 8692847›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Development of Valpha4+ NK T cells in the early stages of embryogenesis.

Y Makino, R Kanno, H Koseki, M Taniguchi

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Invariant NKT Cells and Control of the Thymus Medulla.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  2. Discovery of NKT cells and development of NKT cell-targeted anti-tumor immunotherapy.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2015
    Review
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  12. Requirement for natural killer T (NKT) cells in the induction of allograft tolerance.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  13. Article
  14. Article
  15. Article
  16. Induction of differentiation of pre-NKT cells to mature Valpha14 NKT cells by granulocyte/macrophage colony-stimulating factor.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  17. Natural killer-like nonspecific tumor cell lysis mediated by specific ligand-activated Valpha14 NKT cells.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  18. Article
  19. Essential requirement of an invariant V alpha 14 T cell antigen receptor expression in the development of natural killer T cells.Proceedings of the National Academy of Sciences of the United States of America · 1996
    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

4 authors.

Y MakinoThe Division of Molecular Immunology, Center for Biomedical Science, School of Medicine, Chiba University, Japan.
R Kanno
H Koseki
M Taniguchi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of T lymphocytes start to develop at around day 15 of gestation (d15)-d17 in the thymus and comprise the peripheral repertoire characterized by the expression of polymorphic T-cell antigen receptors (TCRs). Contrary to these conventional T cells, a subset of T cells, called natural killer (NK) T cells (most of them expressing an invariant TCR encoded by the Valpha14Jalpha281 gene with a 1-nt N-region), preferentially differentiates extrathymically and dominates the peripheral T-cell population at a high frequency (5% in splenic T cells and 40% in bone marrow T cells). Here, we investigated the development of NK T cells and found that the invariant Valpha14+ TCR transcripts and the circular DNA created by Valpha14 and Jalpha281 gene rearrangements can be detected in the embryo body at d9.5 of gestation and in the yolk sac and the fetal liver at d11.5-d13.5 of gestation, but not in the thymus, whereas T cells with Valpha1+ TCR expression, a major population in the thymus, were not observed at these early stages of gestation. Fluorescence-activated cell sorter analysis also demonstrated that there exist CD3+ alpha beta+ T cells, almost all of which are Valpha14/Vbeta8+ NK+ T cells, during early embryogenesis. To our knowledge, this demonstrates for the first time that a T lymphocyte subset develops in extrathymic tissues during the early stages of embryogenesis.

Indexed as

AnimalsBase SequenceDNA PrimersEmbryo, MammalianEmbryonic and Fetal DevelopmentFemaleGene Expression Regulation, DevelopmentalKiller Cells, NaturalLiverMiceMice, Inbred BALB CMice, Inbred C57BLMolecular Sequence DataPregnancyReceptors, Antigen, T-CellRNA, MessengerDNA PrimersReceptors, Antigen, T-CellRNA, Messenger

Identifiers

PMID8692847
PMCPMC39055

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.