Evidence map›Paper›PMID 10429669›Full record

ArticleThe Journal of experimental medicine1999

Stem cell emergence and hemopoietic activity are incompatible in mouse intraembryonic sites.

I Godin, J A Garcia-Porrero, F Dieterlen-Lièvre, A Cumano

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Spatiotemporal dynamics of fetal liver hematopoietic niches.The Journal of experimental medicine · 2025
    Article
  3. Review
  4. How cell migration helps immune sentinels.Frontiers in cell and developmental biology · 2022
    Review
  5. Article
  6. JEM career launchpad.The Journal of experimental medicine · 2021
    Article
  7. The mechanisms of pathological extramedullary hematopoiesis in diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
  8. Hematopoiesis: A Layered Organization Across Chordate Species.Frontiers in cell and developmental biology · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Development and differentiation of the erythroid lineage in mammals.Developmental and comparative immunology · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Erythroid development in the mammalian embryo.Blood cells, molecules & diseases · 2013
    Review
  19. Review
  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

4 authors.

I GodinInstitut d'Embryologie Cellulaire et Moléculaire du Centre National de la Recherche Scientifique (CNRS) et du Collège de France, Nogent sur Marne. godin@infobiogen.fr
J A Garcia-Porrero
F Dieterlen-Lièvre
A Cumano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the mouse embryo, the generation of candidate progenitors for long-lasting hemopoiesis has been reported in the paraaortic splanchnopleura (P-Sp)/ aorta-gonad-mesonephros (AGM) region. Here, we address the following question: can the P-Sp/AGM environment support hemopoietic differentiation as well as generate stem cells, and, conversely, are other sites where hemopoietic differentiation occurs capable of generating stem cells? Although P-Sp/AGM generates de novo hemopoietic stem cells between 9.5 and 12.5 days post coitus (dpc), we show here that it does not support hemopoietic differentiation. Among mesoderm-derived sites, spleen and omentum were shown to be colonized by exogenous cells in the same fashion as the fetal liver. Cells colonizing the spleen were multipotent and pursued their evolution to committed progenitors in this organ. In contrast, the omentum, which was colonized by lymphoid-committed progenitors that did not expand, cannot be considered as a hemopoietic organ. From these data, stem cell generation appears incompatible with hemopoietic activity. At the peak of hemopoietic progenitor production in the P-Sp/AGM, between 10.5 and 11.5 dpc, multipotent cells were found at the exceptional frequency of 1 out of 12 total cells and 1 out of 4 AA4.1+ cells. Thus, progenitors within this region constitute a pool of undifferentiated hemopoietic cells readily accessible for characterization.

Indexed as

AnimalsAortaCell DifferentiationCells, CulturedFemaleFlow CytometryGonadsHematopoiesisHematopoietic Stem CellsMaleMesonephrosMiceMice, Inbred BALB CMice, Inbred C57BLOmentumSpleen

Identifiers

PMID10429669
PMCPMC2195563

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.