Evidence map›Paper›PMID 11511541›Full record

ArticleGenes & development2001

Sequential actions of BMP receptors control neural precursor cell production and fate.

D M Panchision, J M Pickel, L Studer, S H Lee, P A Turner, T G Hazel, R D McKay

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing 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

108 citing papers in PubMed, 326 citations in OpenAlex.

  1. Article
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  4. Article
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  7. Regulation of choroid plexus development and its functions.Cellular and molecular life sciences : CMLS · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Single cell RNA sequencing detects persistent cell type- and methylmercury exposure paradigm-specific effects in a human cortical neurodevelopmental model.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Article
  13. Dorsal commissural axon guidance in the developing spinal cord.Current topics in developmental biology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Palmitoylation of BMPR1a regulates neural stem cell fate.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. Article

48 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

D M PanchisionLaboratory of Molecular Biology, NINDS, National Institutes of Health, Bethesda, Maryland 20892-4092, USA.
J M Pickel
L Studer
S H Lee
P A Turner
T G Hazel
R D McKay
National Institute of Neurological Disorders and Stroke · USMemorial Sloan Kettering Cancer Center · USNational Institutes of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone morphogenetic proteins (BMPs) have diverse and sometimes paradoxical effects during embryonic development. To determine the mechanisms underlying BMP actions, we analyzed the expression and function of two BMP receptors, BMPR-IA and BMPR-IB, in neural precursor cells in vitro and in vivo. Neural precursor cells always express Bmpr-1a, but Bmpr-1b is not expressed until embryonic day 9 and is restricted to the dorsal neural tube surrounding the source of BMP ligands. BMPR-IA activation induces (and Sonic hedgehog prevents) expression of Bmpr-1b along with dorsal identity genes in precursor cells and promotes their proliferation. When BMPR-IB is activated, it limits precursor cell numbers by causing mitotic arrest. This results in apoptosis in early gestation embryos and terminal differentiation in mid-gestation embryos. Thus, BMP actions are first inducing (through BMPR-IA) and then terminating (through BMPR-IB), based on the accumulation of BMPR-IB relative to BMPR-IA. We describe a feed-forward mechanism to explain how the sequential actions of these receptors control the production and fate of dorsal precursor cells from neural stem cells.

Indexed as

Trans-ActivatorsAnimalsApoptosisBone Morphogenetic Protein ReceptorsBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsCell CountCell DifferentiationEmbryo, MammalianEpithelial CellsFemaleHedgehog ProteinsMaleMiceMice, Inbred C3HMice, Inbred C57BLBmpr1a protein, mouseBmpr1b protein, mouseBone Morphogenetic Protein ReceptorsBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsHedgehog ProteinsProteinsProtein Serine-Threonine KinasesReceptors, Cell SurfaceReceptors, Growth FactorTrans-Activators

Identifiers

PMID11511541
PMCPMC312756
OpenAlexW2066090522

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.