Evidence map›Paper›PMID 33230302›Full record

ArticleNature cell biology2020

Manipulating niche composition limits damage to haematopoietic stem cells during Plasmodium infection.

Myriam L R Haltalli, Samuel Watcham, Nicola K Wilson, Kira Eilers, Alexander Lipien, Heather Ang, Flora Birch, Sara Gonzalez Anton, Chiara Pirillo, Nicola Ruivo and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  6. Differential Response and Recovery Dynamics of HSPC Populations FollowingInternational journal of molecular sciences · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Schistosome Infection Impacts Hematopoiesis.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Osteoblast Lineage Support of Hematopoiesis in Health and Disease.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. 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

19 authors at 6 institutions in 3 countries.

Myriam L R HaltalliDepartment of Life Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-0886-4466
Samuel WatchamWellcome-Medical Research Council Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-8399-7875
Nicola K WilsonWellcome-Medical Research Council Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
Kira EilersDepartment of Life Sciences, Imperial College London, London, UK.
Alexander LipienDepartment of Life Sciences, Imperial College London, London, UK.
Heather AngDepartment of Life Sciences, Imperial College London, London, UK.
Flora BirchDepartment of Life Sciences, Imperial College London, London, UK.
Sara Gonzalez AntonDepartment of Life Sciences, Imperial College London, London, UK.
Chiara PirilloDepartment of Life Sciences, Imperial College London, London, UK.
Nicola RuivoDepartment of Life Sciences, Imperial College London, London, UK.
Maria L VainieriDepartment of Life Sciences, Imperial College London, London, UK.
Constandina PosporiDepartment of Life Sciences, Imperial College London, London, UK.
Robert E SindenDepartment of Life Sciences, Imperial College London, London, UK.
Tiago C LuisDepartment of Life Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-6305-1257
Jean LanghorneThe Francis Crick Institute, London, UK.
Ken R DuffyHamilton Institute, Maynooth University, Maynooth, Ireland.ORCID http://orcid.org/0000-0001-5587-9356
Berthold GöttgensWellcome-Medical Research Council Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-6302-5705
Andrew M BlagboroughDepartment of Pathology, University of Cambridge, Cambridge, UK.
Cristina Lo CelsoDepartment of Life Sciences, Imperial College London, London, UK. c.lo-celso@imperial.ac.uk.ORCID http://orcid.org/0000-0002-1163-4207
Imperial College London · GBThe Francis Crick Institute · GBWellcome/MRC Cambridge Stem Cell Institute · GBAO Foundation · CHNational University of Ireland, Maynooth · IEUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L023776/1Cancer Research UK 21762Medical Research Council MC_PC_12009Medical Research Council MR/M008975/1Medical Research Council MR/N00227X/1Wellcome Trust 105398/Z/14/ZWellcome Trust 206328/Z/17/ZWellcome Trust 210424/Z/18/ZWellcome Trust 212304Wellcome Trust 212304/Z/18/Z
6 · The paper itself

Abstract

Severe infections are a major stress on haematopoiesis, where the consequences for haematopoietic stem cells (HSCs) have only recently started to emerge. HSC function critically depends on the integrity of complex bone marrow (BM) niches; however, what role the BM microenvironment plays in mediating the effects of infection on HSCs remains an open question. Here, using a murine model of malaria and combining single-cell RNA sequencing, mathematical modelling, transplantation assays and intravital microscopy, we show that haematopoiesis is reprogrammed upon infection, whereby the HSC compartment turns over substantially faster than at steady-state and HSC function is drastically affected. Interferon is found to affect both haematopoietic and mesenchymal BM cells and we specifically identify a dramatic loss of osteoblasts and alterations in endothelial cell function. Osteo-active parathyroid hormone treatment abolishes infection-triggered HSC proliferation and-coupled with reactive oxygen species quenching-enables partial rescuing of HSC function.

Indexed as

AnimalsBone Marrow CellsEndothelial CellsGene Expression ProfilingHematopoiesisHematopoietic Stem CellsHumansMalariaMesenchymal Stem CellsMice, Inbred C57BLMice, KnockoutOsteoblastsParathyroid HormonePlasmodium bergheiReactive Oxygen SpeciesStem Cell NicheParathyroid HormoneReactive Oxygen Species

Identifiers

PMID33230302
PMCPMC7611033
OpenAlexW3110058853

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.