Evidence map›Paper›PMID 29899037›Full record

ArticleThe Journal of experimental medicine2018

Dissection of progenitor compartments resolves developmental trajectories in B-lymphopoiesis.

Christina T Jensen, Josefine Åhsberg, Mikael N E Sommarin, Tobias Strid, Rajesh Somasundaram, Kazuki Okuyama, Jonas Ungerbäck, Jussi Kupari, Matti S Airaksinen, Stefan Lang and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Function of E2A in B-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. EBF1 is continuously required for stabilizing local chromatin accessibility in pro-B cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Molecular Regulation of Differentiation in Early B-Lymphocyte Development.International journal of molecular sciences · 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

14 authors at 3 institutions in 2 countries.

Christina T JensenDivision of Molecular Hematology, Lund University, Lund, Sweden.
Josefine ÅhsbergDivision of Molecular Hematology, Lund University, Lund, Sweden.
Mikael N E SommarinDivision of Molecular Hematology, Lund University, Lund, Sweden.ORCID 0000-0002-2581-5543
Tobias StridDivision of Molecular Hematology, Lund University, Lund, Sweden.
Rajesh SomasundaramDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.ORCID 0000-0003-0669-9644
Kazuki OkuyamaDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Jonas UngerbäckDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.ORCID 0000-0002-2190-3896
Jussi KupariFaculty of Medicine, University of Helsinki, Helsinki, Finland.
Matti S AiraksinenFaculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-7199-4984
Stefan LangDivision of Molecular Hematology, Lund University, Lund, Sweden.ORCID 0000-0002-0854-2328
David BryderDivision of Molecular Hematology, Lund University, Lund, Sweden.
Shamit SonejiDivision of Molecular Hematology, Lund University, Lund, Sweden.
Göran KarlssonDivision of Molecular Hematology, Lund University, Lund, Sweden.
Mikael SigvardssonDivision of Molecular Hematology, Lund University, Lund, Sweden mikael.sigvardsson@med.lu.se.ORCID 0000-0001-8527-7276
Lund University · SELinköping University · SEUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To understand the developmental trajectories in early lymphocyte differentiation, we identified differentially expressed surface markers on lineage-negative lymphoid progenitors (LPs). Single-cell polymerase chain reaction experiments allowed us to link surface marker expression to that of lineage-associated transcription factors (TFs) and identify GFRA2 and BST1 as markers of early B cells. Functional analyses in vitro and in vivo as well as single-cell gene expression analyses supported that surface expression of these proteins defined distinct subpopulations that include cells from both the classical common LPs (CLPs) and Fraction A compartments. The formation of the GFRA2-expressing stages of development depended on the TF EBF1, critical both for the activation of stage-specific target genes and modulation of the epigenetic landscape. Our data show that consecutive expression of Ly6D, GFRA2, and BST1 defines a developmental trajectory linking the CLP to the CD19

Indexed as

Cell CompartmentationLymphopoiesisADP-ribosyl CyclaseAnimalsAntigens, CDAntigens, LyB-LymphocytesBone MarrowCell LineageCell MembraneGlial Cell Line-Derived Neurotrophic Factor ReceptorsGPI-Linked ProteinsMiceModels, BiologicalStem CellsADP-ribosyl CyclaseADP-ribosyl cyclase 2Antigens, CDAntigens, LyGfra2 protein, mouseGlial Cell Line-Derived Neurotrophic Factor ReceptorsGPI-Linked ProteinsLy6d protein, mouse

Identifiers

PMID29899037
PMCPMC6028518
OpenAlexW2808211240

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.