Evidence map›Paper›PMID 35922411›Full record

ArticleNature communications2022

Fate mapping of hematopoietic stem cells reveals two pathways of native thrombopoiesis.

Mina N F Morcos, Congxin Li, Clara M Munz, Alessandro Greco, Nicole Dressel, Susanne Reinhardt, Katrin Sameith, Andreas Dahl, Nils B Becker, Axel Roers and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Inferring Cell Differentiation Dynamics with Unobserved Progenitors.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Mapping Hematopoietic Fate after Transplantation.Stem cell reviews and reports · 2025
    Review
  8. Article
  9. Article
  10. Direct megakaryopoiesis.Current opinion in hematology · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

12 authors.

Mina N F Morcos *Institute for Immunology, Faculty of Medicine, TU Dresden, 01307, Dresden, Germany.ORCID 0000-0001-5812-9526
Congxin Li *Division of Theoretical Systems Biology, German Cancer Research Center, 69120, Heidelberg, Germany.
Clara M Munz *Institute for Immunology, Faculty of Medicine, TU Dresden, 01307, Dresden, Germany.
Alessandro GrecoDivision of Theoretical Systems Biology, German Cancer Research Center, 69120, Heidelberg, Germany.ORCID 0000-0002-6453-1666
Nicole DresselInstitute for Immunology, Faculty of Medicine, TU Dresden, 01307, Dresden, Germany.
Susanne ReinhardtDRESDEN-concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, 01307, Dresden, Germany.ORCID 0000-0001-9202-105X
Katrin SameithDRESDEN-concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, 01307, Dresden, Germany.ORCID 0000-0003-4306-930X
Andreas DahlDRESDEN-concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, 01307, Dresden, Germany.ORCID 0000-0002-2668-8371
Nils B BeckerDivision of Theoretical Systems Biology, German Cancer Research Center, 69120, Heidelberg, Germany.
Axel RoersInstitute for Immunology, Heidelberg University Hospital, 69120, Heidelberg, Germany.ORCID 0000-0003-1806-6158
Thomas HöferDivision of Theoretical Systems Biology, German Cancer Research Center, 69120, Heidelberg, Germany. t.hoefer@dkfz.de.ORCID 0000-0003-3560-8780
Alexander GerbauletInstitute for Immunology, Faculty of Medicine, TU Dresden, 01307, Dresden, Germany. alexander.gerbaulet@tu-dresden.de.ORCID 0000-0003-4680-4920

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs) produce highly diverse cell lineages. Here, we chart native lineage pathways emanating from HSCs and define their physiological regulation by computationally integrating experimental approaches for fate mapping, mitotic tracking, and single-cell RNA sequencing. We find that lineages begin to split when cells leave the tip HSC population, marked by high Sca-1 and CD201 expression. Downstream, HSCs either retain high Sca-1 expression and the ability to generate lymphocytes, or irreversibly reduce Sca-1 level and enter into erythro-myelopoiesis or thrombopoiesis. Thrombopoiesis is the sum of two pathways that make comparable contributions in steady state, a long route via multipotent progenitors and CD48

Indexed as

Hematopoietic Stem CellsThrombopoiesisCell DifferentiationCell LineageMyelopoiesis

Identifiers

PMID35922411
PMCPMC9349191

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.