Evidence map›Paper›PMID 23765990›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2013

Investigation of retinoic acid function during embryonic brain development using retinaldehyde-rescued Rdh10 knockout mice.

Christina Chatzi, Thomas J Cunningham, Gregg Duester

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  5. Review
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  9. Review
  10. Developmental biology of the meninges.Genesis (New York, N.Y. : 2000) · 2019
    Review
  11. Article
  12. Article
  13. New insights and changing paradigms in the regulation of vitamin A metabolism in development.Wiley interdisciplinary reviews. Developmental biology · 2017
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Wnt8a and Wnt3a cooperate in the axial stem cell niche to promote mammalian body axis extension.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
  20. Input overload: Contributions of retinoic acid signaling feedback mechanisms to heart development and teratogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    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

3 authors at 1 institution in 1 country.

Christina ChatziSanford-Burnham Medical Research Institute, La Jolla, California, USA.
Thomas J Cunningham
Gregg Duester
Sanford Burnham Prebys Medical Discovery Institute · US

Funding

Animal Model to Study Retinoic Acid Function in Postnatal and Adult TissuesR21OD011181 · OD · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI DUESTER, GREGG L · 2012 to 2012
$244k
NIH HHS OD011181NIH HHS R21 OD011181
6 · The paper itself

Abstract

backgroundRetinoic acid (RA) signaling controls patterning and neuronal differentiation within the hindbrain, but forebrain RA function remains controversial. RA is produced from metabolism of retinol to retinaldehyde by retinol dehydrogenase (RDH), followed by metabolism of retinaldehyde to RA by retinaldehyde dehydrogenase (RALDH). Previous studies on Raldh2-/- and Raldh3-/- mice demonstrated an RA requirement for γ-aminobutyric acid (GABA)ergic and dopaminergic differentiation in forebrain basal ganglia, but no RA requirement was observed during early forebrain patterning or subsequent forebrain cortical expansion. However, other studies suggested that RA controls forebrain patterning, and analysis of ethylnitrosourea-induced Rdh10 mutants suggested that RA synthesized in the meninges stimulates forebrain cortical expansion.

resultsWe generated Rdh10-/- mouse embryos that lack RA activity early in the head and later in the meninges. We observed defects in hindbrain patterning and eye RA signaling, but early forebrain patterning was unaffected. Retinaldehyde treatment of Rdh10-/- embryos from E7-E9 rescues a cranial skeletal defect, resulting in E14.5 embryos lacking meningeal RA activity but maintaining normal forebrain shape and cortical expansion.

conclusionsRdh10-/- embryos demonstrate that RA controls hindbrain but not early forebrain patterning, while studies on retinaldehyde-rescued Rdh10-/- embryos show that meningeal RA synthesis is unnecessary to stimulate forebrain cortical expansion.

Indexed as

Alcohol OxidoreductasesAnimalsEmbryo, MammalianEyeMiceMice, KnockoutNeurogenesisProsencephalonRetinaldehydeSignal TransductionTretinoinAlcohol OxidoreductasesRetinaldehydetrans-retinol dehydrogenaseTretinoincortexforebrainhindbrainmeningesRdh10 knockoutretinaldehyderetinoic acid

Identifiers

PMID23765990
PMCPMC3877746
OpenAlexW1698017871

What OpenQuestion holds

Textmetadata
LicenceTDM
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.