Evidence map›Paper›PMID 17488818›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Caspase-9 regulates apoptosis/proliferation balance during metamorphic brain remodeling in Xenopus.

Laurent Coen, Karine Le Blay, Isaline Rowe, Barbara A Demeneix

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
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  7. Article
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  9. Article
  10. Article
  11. Review
  12. Shaping organisms with apoptosis.Cell death and differentiation · 2013
    Review
  13. Article
  14. Article
  15. Apoptosis in amphibian organs during metamorphosis.Apoptosis : an international journal on programmed cell death · 2010
    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

4 authors at 1 institution in 1 country.

Laurent CoenEvolution des Régulations Endocriniennes, Muséum National d'Histoire Naturelle, Unité Mixte de Recherche-Centre National de la Recherche Scientifique 5166, Unité Scientifique du Muséum 501, Paris, France.
Karine Le Blay
Isaline Rowe
Barbara A Demeneix
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During anuran metamorphosis, the tadpole brain is transformed producing the sensorial and motor systems required for the frog's predatory lifestyle. Nervous system remodeling simultaneously implicates apoptosis, cell division, and differentiation. The molecular mechanisms underlying this remodeling have yet to be characterized. Starting from the observation that active caspase-9 and the Bcl-X(L) homologue, XR11 are highly expressed in tadpole brain during metamorphosis, we determined their implication in regulating the balance of apoptosis and proliferation in the developing tadpole brain. In situ hybridization showed caspase-9 mRNA to be expressed mainly in the ventricular area, a site of neuroblast proliferation. To test the functional role of caspase-9 in equilibrating neuroblast production and elimination, we overexpressed a dominant-negative caspase-9 protein, DN9, in the tadpole brain using somatic gene transfer and germinal transgenesis. In both cases, abrogating caspase-9 activity significantly decreased brain apoptosis and increased numbers of actively proliferating cells in the ventricular zone. Moreover, overexpression of XR11 with or without DN9 was also effective in decreasing apoptosis and increasing cell division in the tadpole brain. We conclude that XR11 and caspase-9, two key members of the mitochondrial death pathway, are implicated in controlling the proliferative status of neuroblasts in the metamorphosing Xenopus brain. Modification of their expression during the critical period of metamorphosis alters the outcome of metamorphic neurogenesis, resulting in a modified brain phenotype in juvenile Xenopus.

Indexed as

ApoptosisAnimalsAnimals, Genetically Modifiedbcl-X ProteinBrainCaspase 9Cell ProliferationCell SurvivalCerebral VentriclesEnzyme ActivationGene Expression Regulation, EnzymologicGenes, DominantLarvaMetamorphosis, BiologicalMitosisRNA, MessengerBCL2L1 protein, Xenopusbcl-X ProteinCaspase 9RNA, MessengerXenopus Proteins

Identifiers

PMID17488818
PMCPMC1895979
OpenAlexW2001784209

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.