Document Detail


Retinoic acid receptor (RAR)-alpha is not critically required for mediating retinoic acid effects in the developing mouse retina.
MedLine Citation:
PMID:  20107170     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
PURPOSE: To determine the functional contribution of retinoic acid receptor (RAR)-alpha in the developing murine neural retina, through a phenotypic analysis of the corresponding null mutants. METHODS: RARalpha mutant (Rara(-/-)) mice were compared with wild-type littermates at several stages of pre- and postnatal development. An RA-response element (RARE)-containing reporter transgene was used to assess the contribution of RARalpha to retinoid signaling in the retina. In situ hybridization was performed on serial eye sections to investigate the expression of main developmental regulators. Immunofluorescence was used to detect differentiated cell types in the adult retina. Mutants were also subjected to clinical observation and visual function evaluation with the optomotor test and electroretinography. RESULTS: Both isoform transcripts of RARalpha were expressed throughout the neural retina at various stages of pre- and postnatal development. In the Rara(-/-) mice the RARE-reporter transgene consistently failed to activate in the developing neural retina. However, they did not exhibit any alteration of the expression patterns of molecular determinants and had a normal organization of retinal cell types at postnatal stages. Their performance in visual tests was indistinguishable from that of control littermates. CONCLUSIONS: Although RARalpha mediates RARE reporter transgene activity in the neural retina, its function is not necessary for the retina to develop and function normally. These data suggest that retinoic acid regulates neural retinal development through other, possibly RAR-independent, pathways.
Authors:
Laura Cammas; Fr?d?ric Trensz; Abdeljalil Jellali; Norbert B Ghyselinck; Michel J Roux; Pascal Doll?
Publication Detail:
Type:  Journal Article     Date:  2010-01-27
Journal Detail:
Title:  Investigative ophthalmology & visual science     Volume:  51     ISSN:  1552-5783     ISO Abbreviation:  Invest. Ophthalmol. Vis. Sci.     Publication Date:  2010 Jun 
Date Detail:
Created Date:  2010-05-20     Completed Date:  2010-06-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7703701     Medline TA:  Invest Ophthalmol Vis Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  3281-90     Citation Subset:  IM    
Affiliation:
Institut de G?n?tique et de Biologie Mol?culaire et Cellulaire, BP 10142 Illkirch, France.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Differentiation
Electroretinography
Embryonic Development / physiology
Fluorescein Angiography
Fluorescent Antibody Technique, Indirect
Gene Expression Regulation / physiology
Genes, Reporter
In Situ Hybridization
Mice
Mice, Knockout
Mice, Transgenic
Motor Activity
Protein Isoforms
Receptors, Retinoic Acid / physiology*
Response Elements
Retina / embryology*,  metabolism
Tretinoin / physiology*
Chemical
Reg. No./Substance:
0/Protein Isoforms; 0/Receptors, Retinoic Acid; 0/retinoic acid receptor alpha; 302-79-4/Tretinoin

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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