Evidence map›Paper›PMID 17896863›Full record

ArticlePLoS biology2007

Negative autoregulation by FAS mediates robust fetal erythropoiesis.

Merav Socolovsky, Michael Murrell, Ying Liu, Ramona Pop, Ermelinda Porpiglia, Andre Levchenko

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. HES1 is required for mouse fetal hematopoiesis.Stem cell research & therapy · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Delta-Globin Gene Expression Is EnhancedFrontiers in medicine · 2020
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  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

6 authors at 2 institutions in 1 country.

Merav SocolovskyDepartment of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America. merav.socolovsky@umassmed.edu
Michael Murrell
Ying Liu
Ramona Pop
Ermelinda Porpiglia
Andre Levchenko
University of Massachusetts Chan Medical School · USJohns Hopkins University · US

Funding

TCP5: ACTIVE SITE LABELING REAGENT FOR ACETYLTRANSFERASESU54RR020839 · NCRR · JOHNS HOPKINS UNIVERSITY · PI BOEKE, JEF D · 2004 to 2011
$27.4M
Molecular Analysis of the Erythropoietic Stress Response in vivoR01HL084168 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SOCOLOVSKY, MERAV · 2006 to 2010
$2.1M
NCRR NIH HHS U54 RR020839NCRR NIH HHS U54-RR020839NHLBI NIH HHS R01 HL084168NHLBI NIH HHS R01 HL084168-01
6 · The paper itself

Abstract

Tissue development is regulated by signaling networks that control developmental rate and determine ultimate tissue mass. Here we present a novel computational algorithm used to identify regulatory feedback and feedforward interactions between progenitors in developing erythroid tissue. The algorithm makes use of dynamic measurements of red cell progenitors between embryonic days 12 and 15 in the mouse. It selects for intercellular interactions that reproduce the erythroid developmental process and endow it with robustness to external perturbations. This analysis predicts that negative autoregulatory interactions arise between early erythroblasts of similar maturation stage. By studying embryos mutant for the death receptor FAS, or for its ligand, FASL, and by measuring the rate of FAS-mediated apoptosis in vivo, we show that FAS and FASL are pivotal negative regulators of fetal erythropoiesis, in the manner predicted by the computational model. We suggest that apoptosis in erythroid development mediates robust homeostasis regulating the number of red blood cells reaching maturity.

Indexed as

AlgorithmsAnimalsApoptosisCell DifferentiationCell SeparationErythrocytesErythroid Precursor CellsErythropoiesisFas Ligand Proteinfas ReceptorFeedback, PhysiologicalFetusFlow CytometryHomeostasisLiverMiceFas Ligand ProteinFasl protein, mouseFas protein, mousefas Receptor

Identifiers

PMID17896863
PMCPMC1988857
OpenAlexW2088024298

What OpenQuestion holds

Textmetadata
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.