Evidence map›Paper›PMID 30803026›Full record

ArticleImmunology and cell biology2019

Divergent SATB1 expression across human life span and tissue compartments.

Simone Nüssing, Hui-Fern Koay, Sneha Sant, Thomas Loudovaris, Stuart I Mannering, Martha Lappas, Yves D Udekem, Igor E Konstantinov, Stuart P Berzins, Guus F Rimmelzwaan and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Running to Stand Still: Naive CD8International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. The Role of SATB1 in Tumour Progression and Metastasis.International journal of molecular sciences · 2019
    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

15 authors at 7 institutions in 3 countries.

Simone NüssingDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Hui-Fern KoayDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Sneha SantDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Thomas LoudovarisImmunology and Diabetes Unit, St Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
Stuart I ManneringImmunology and Diabetes Unit, St Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
Martha LappasObstetrics, Nutrition and Endocrinology Group, Department of Obstetrics & Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, VIC, Australia.
Yves D UdekemDepartment of Cardiothoracic Surgery, Royal Children's Hospital and Melbourne Children's Centre for Cardiovascular Genomics and Regenerative Medicine, Parkville, VIC, Australia.
Igor E KonstantinovDepartment of Cardiothoracic Surgery, Royal Children's Hospital and Melbourne Children's Centre for Cardiovascular Genomics and Regenerative Medicine, Parkville, VIC, Australia.
Stuart P BerzinsDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Guus F RimmelzwaanDepartment of Viroscience, Erasmus Medical Centre, Rotterdam, The Netherlands.
Stephen J TurnerDepartment of Microbiology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
E Bridie ClemensDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Dale I GodfreyDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Thi Ho NguyenDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
Katherine KedzierskaDepartment of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Parkville, VIC, Australia.
University of Melbourne · AUPeter Doherty Institute · AURoyal Children's Hospital · AUErasmus University Rotterdam · NLMonash University · AUSt Vincent's Hospital · AUSt Vincents Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Special AT-rich binding protein-1 (SATB1) is a global chromatin organizer capable of activating or repressing gene transcription in mice and humans. The role of SATB1 is pivotal for T-cell development, with SATB1-knockout mice being neonatally lethal, although the exact mechanism is unknown. Moreover, SATB1 is dysregulated in T-cell lymphoma and proposed to suppress transcription of the Pdcd1 gene, encoding the immune checkpoint programmed cell death protein 1 (PD-1). Thus, SATB1 expression in T-cell subsets across different tissue compartments in humans is of potential importance for targeting PD-1. Here, we comprehensively analyzed SATB1 expression across different human tissues and immune compartments by flow cytometry and correlated this with PD-1 expression. We investigated SATB1 protein levels in pediatric and adult donors and assessed expression dynamics of this chromatin organizer across different immune cell subsets in human organs, as well as in antigen-specific T cells directed against acute and chronic viral infections. Our data demonstrate that SATB1 expression in humans is the highest in T-cell progenitors in the thymus, and then becomes downregulated in mature T cells in the periphery. Importantly, SATB1 expression in peripheral mature T cells is not static and follows fine-tuned expression dynamics, which appear to be tissue- and antigen-dependent. Furthermore, SATB1 expression negatively correlates with PD-1 expression in virus-specific CD8

Indexed as

AgingMatrix Attachment Region Binding ProteinsAdultAgedCD8-Positive T-LymphocytesChild, PreschoolFemaleGene Expression RegulationHumansInfantInfant, NewbornMaleMiddle AgedOrgan SpecificityProgrammed Cell Death 1 ReceptorThymocytesMatrix Attachment Region Binding ProteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorSATB1 protein, humanHuman CD8+ T cellsPD-1SATB1

Identifiers

PMID30803026
PMCPMC6618325
OpenAlexW2917649342

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.