Evidence map›Paper›PMID 35603697›Full record

ArticleBiology open2022

Intrinsic function of the peptidylarginine deiminase PADI4 is dispensable for normal haematopoiesis.

Christine Young, John R Russell, Louie N Van De Lagemaat, Hannah Lawson, Christopher Mapperley, Kamil R Kranc, Maria A Christophorou

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Transcriptomic analysis of PADI4 target genes during multi-lineage differentiation of embryonic stem cells.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Article
  5. Article
  6. The virtues and vices of protein citrullination.Royal Society open science · 2022
    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

7 authors at 4 institutions in 1 country.

Christine YoungMRC Human Genetics Unit, The Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
John R RussellMRC Human Genetics Unit, The Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Louie N Van De LagemaatCentre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Hannah LawsonCentre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Christopher MapperleyCentre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Kamil R KrancCentre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Maria A ChristophorouMRC Human Genetics Unit, The Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.ORCID 0000-0001-5455-7283
Queen Mary University of London · GBBabraham Institute · GBInstitute of Genetics and Cancer · GBMRC Centre for Regenerative Medicine · GB

Funding

Cancer Research UK 14633Cancer Research UK 26787Cancer Research UK C29967/A26787Medical Research Council MR/P010008/1Medical Research Council MR/P010008/2Wellcome TrustWellcome Trust 105642/Z/14/Z
6 · The paper itself

Abstract

Peptidylarginine deiminases (PADIs) are strongly associated with the development of autoimmunity, neurodegeneration and cancer but their physiological roles are ill-defined. The nuclear deiminase PADI4 regulates pluripotency in the mammalian pre-implantation embryo but its function in tissue development is unknown. PADI4 is primarily expressed in the bone marrow, as part of a self-renewal-associated gene signature. It has been shown to regulate the proliferation of multipotent haematopoietic progenitors and proposed to impact on the differentiation of haematopoietic stem cells (HSCs), suggesting that it controls haematopoietic development or regeneration. Using conditional in vivo models of steady state and acute Padi4 ablation, we examined the role of PADI4 in the development and function of the haematopoietic system. We found that PADI4 loss does not significantly affect HSC self-renewal or differentiation potential upon injury or serial transplantation, nor does it lead to HSC exhaustion or premature ageing. Thus PADI4 is dispensable for cell-autonomous HSC maintenance, differentiation and haematopoietic regeneration. This work represents the first study of PADI4 in tissue development and indicates that pharmacological PADI4 inhibition may be tolerated without adverse effects.

Indexed as

HydrolasesMammalsAnimalsCell DifferentiationProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4HydrolasesProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4AgeingBone marrowDifferentiationHaematopoietic developmentPeptidylarginine deiminase IV (PADI4)Regeneration

Identifiers

PMID35603697
PMCPMC9212077
OpenAlexW4281395285

What OpenQuestion holds

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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.