Evidence map›Paper›PMID 20064453›Full record

ArticleImmunity2009

Spatial mapping of thymic stromal microenvironments reveals unique features influencing T lymphoid differentiation.

Ann V Griffith, Mohammad Fallahi, Hiroshi Nakase, Mark Gosink, Brandon Young, Howard T Petrie

Abstract read
In one paragraph

Article in Immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Fetal Thymic Organ Culture and Negative Selection.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Redox status regulates autophagy in thymic stromal cells and promotes T cell tolerance.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Cytokines, Transcription Factors, and the Initiation of T-Cell Development.Cold Spring Harbor perspectives in biology · 2018
    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

6 authors.

Ann V GriffithDepartment of Cancer Biology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Mohammad Fallahi
Hiroshi Nakase
Mark Gosink
Brandon Young
Howard T Petrie

Funding

Control of precursor thymocyte differentiatonR01AI033940 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PETRIE, HOWARD T. · 2001 to 2009
$2.9M
Notch3 in generation and maintenance of the T lineage.R01AG034876 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI PETRIE, HOWARD T. · 2009 to 2013
$2.3M
Identification of stromal responses during castration-induced thymic regrowth.R01AG031576 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI PETRIE, HOWARD T. · 2009 to 2014
$2.0M
Control of precursor thymocyte differentiation.R56AI033940 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PETRIE, HOWARD T. · 2010 to 2010
$486k
Transcriptional Mapping of Thymic Stromal Microenvironments`R21AI067453 · NIAID · SCRIPPS FLORIDA · PI PETRIE, HOWARD T. · 2006 to 2007
$376k
CONTROL OF PRECURSOR THYMOCYTE DIFFERENTIATIONR21AI033940 · NIAID · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PETRIE, HOWARD T. · 2000 to 2000
$322k
SELECTION AND CELL DEATH IN T CELL DEVELOPMENTR29AI033940 · NIAID · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PETRIE, HOWARD T. · 1994 to 1998
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NIAID NIH HHS AI033940NIAID NIH HHS AI067453NIAID NIH HHS R01 AI033940NIAID NIH HHS R21 AI033940NIAID NIH HHS R21 AI067453NIAID NIH HHS R29 AI033940NIAID NIH HHS R56 AI033940NIA NIH HHS AG031576NIA NIH HHS R01 AG031576NIA NIH HHS R01 AG034876
6 · The paper itself

Abstract

Interaction of hematopoietic progenitors with the thymic microenvironment induces them to proliferate, adopt the T lineage fate, and asymmetrically diverge into multiple functional lineages. Progenitors at various developmental stages are stratified within the thymus, implying that the corresponding microenvironments provide distinct sets of signals to progenitors migrating between them. These differences remain largely undefined. Here we used physical and computational approaches to generate a comprehensive spatial map of stromal gene expression in the thymus. Although most stromal regions were characterized by a unique gene expression signature, the central cortex lacked distinctive features. Instead, a key function of this region appears to be the sequestration of unique microenvironments found at the cortical extremities, thus modulating the relative proximity of progenitors moving between them. Our findings compel reexamination of how cell migration, lineage specification, and proliferation are controlled by thymic architecture and provide an in-depth resource for global characterization of this control.

Indexed as

AnimalsCell DifferentiationCell MovementGene Expression ProfilingLymphoid Progenitor CellsMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisSignal TransductionStromal CellsThymus GlandT-Lymphocyte Subsets

Identifiers

PMID20064453
PMCPMC2807413

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.