Evidence map›Paper›PMID 25838284›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

PLZF expression maps the early stages of ILC1 lineage development.

Michael G Constantinides, Herman Gudjonson, Benjamin D McDonald, Isabel E Ishizuka, Philip A Verhoef, Aaron R Dinner, Albert Bendelac

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

97 citing papers in PubMed, 155 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. T cells in health and disease.Signal transduction and targeted therapy · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Purification of Bone Marrow Precursors to T Cells and ILCs.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  16. Early Development of Innate Lymphoid Cells.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  17. Identification of aceNKPs, a committed common progenitor population of the ILC1 and NK cell continuum.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Article
  19. Article
  20. Article

37 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

7 authors at 1 institution in 1 country.

Michael G ConstantinidesCommittee on Immunology.
Herman GudjonsonInstitute for Biophysical Dynamics, and.
Benjamin D McDonaldCommittee on Immunology.
Isabel E IshizukaCommittee on Immunology.
Philip A VerhoefCommittee on Immunology.
Aaron R DinnerCommittee on Immunology, Institute for Biophysical Dynamics, and Department of Chemistry, University of Chicago, Chicago, IL 60637.
Albert BendelacCommittee on Immunology, abendela@bsd.uchicago.edu.
University of Chicago · US

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI LIU, CAMBRIAN YANGSHAO · 1990 to 2025
$29.8M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
RESEARCH TRAINING IN RESPIRATORY BIOLOGYT32HL007605 · NHLBI · UNIVERSITY OF CHICAGO · PI Yun Fang, Gokhan M. Mutlu · 1985 to 2026
$18.1M
Transcriptional Regulation of Innate-Like T CellsR01AI038339 · NIAID · UNIVERSITY OF CHICAGO · PI ESTERHAZY, DARIA · 1996 to 2025
$7.6M
Graduate Program in Biophysical Sciences at the University of Chicago - Renewal 0T32EB009412 · NIBIB · UNIVERSITY OF CHICAGO · PI ENGEL, GREGORY S, SOSNICK, TOBIN R · 2009 to 2023
$4.9M
Transcriptional Regulation of Innate-Like T CellsR37AI038339 · NIAID · UNIVERSITY OF CHICAGO · PI BENDELAC, ALBERT S. · 2017 to 2023
$3.4M
A common hematopoietic precursor to innate lymphoid cellsR01AI108643 · NIAID · UNIVERSITY OF CHICAGO · PI BENDELAC, ALBERT S. · 2014 to 2017
$1.5M
Allergic inflammation in genetic models of lung ILC2 deficiencyR01HL118092 · NHLBI · UNIVERSITY OF CHICAGO · PI BENDELAC, ALBERT S. · 2013 to 2016
$1.5M
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS HL118092NHLBI NIH HHS R01 HL118092NHLBI NIH HHS T32 HL007605NIAID NIH HHS AI038339NIAID NIH HHS R01 AI038339NIAID NIH HHS R01 AI108643NIBIB NIH HHS T32 EB009412NIDDK NIH HHS P30 DK042086NIDDK NIH HHS P30 DK42086
6 · The paper itself

Abstract

Among the variety of tissue-resident NK-like populations recently distinguished from recirculating classical NK (cNK) cells, liver innate lymphoid cells (ILC) type 1 (ILC1s) have been shown to represent a distinct lineage that originates from a novel promyelocytic leukaemia zinc finger (PLZF)-expressing ILC precursor (ILCP) strictly committed to the ILC1, ILC2, and ILC3 lineages. Here, using PLZF-reporter mice and cell transfer assays, we studied the developmental progression of ILC1s and demonstrated substantial overlap with stages previously ascribed to the cNK lineage, including pre-pro-NK, pre-NK precursor (pre-NKP), refined NKP (rNKP), and immature NK (iNK). Although they originated from different precursors, the ILC1 and cNK lineages followed a parallel progression at early stages and diverged later at the iNK stage, with a striking predominance of ILC1s over cNKs early in ontogeny. Although a limited set of ILC1 genes depended on PLZF for expression, characteristically including Il7r, most of these genes were also differentially expressed between ILC1s and cNKs, indicating that PLZF together with other, yet to be defined, factors contribute to the divergence between these lineages.

Indexed as

Cell LineageImmunity, InnateAnimalsAnimals, NewbornAntigens, LyBone Marrow CellsCell DifferentiationFetusGene Expression ProfilingKiller Cells, NaturalKruppel-Like Transcription FactorsLiverLymphocytesMice, Inbred C57BLNK Cell Lectin-Like Receptor Subfamily BPromyelocytic Leukemia Zinc Finger ProteinAntigens, LyKlrb1c protein, mouseKruppel-Like Transcription FactorsNK Cell Lectin-Like Receptor Subfamily BPromyelocytic Leukemia Zinc Finger ProteinZbtb16 protein, mouseILC1innate lymphoid celllymphocyte developmentNK cellPLZF

Identifiers

PMID25838284
PMCPMC4413309
OpenAlexW2030387968

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.