Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
16
pubmed:dateCreated
1995-9-11
pubmed:abstractText
We have recently characterized a cardiac model of ventricular chamber defects in retinoid X receptor alpha (RXR alpha) homozygous mutant (-/-) gene-targeted mice. These mice display generalized edema, ventricular chamber hypoplasia, and muscular septal defects, and they die at embryonic day 15. To substantiate our hypothesis that the embryos are dying of cardiac pump failure, we have used digital bright-field and fluorescent video microscopy and in vivo microinjection of fluorescein-labeled albumin to analyze cardiac function. The affected embryos showed depressed ventricular function (average left ventricular area ejection fraction, 14%), ventricular septal defects, and various degrees of atrioventricular block not seen in the RXR alpha wild-type (+/+) and heterozygous (+/-) littermates (average left ventricular area ejection fraction, 50%). The molecular mechanisms involved in these ventricular defects were studied by evaluating expression of cardiac-specific genes known to be developmentally regulated. By in situ hybridization, aberrant, persistent expression of the atrial isoform of myosin light chain 2 was identified in the ventricles. We hypothesize that retinoic acid provides a critical signal mediated through the RXR alpha pathway that is required to allow progression of development of the ventricular region of the heart from its early atrial-like form to the thick-walled adult ventricle. The conduction system disturbances found in the RXR alpha -/- embryos may reflect a requirement of the developing conduction system for the RXR alpha signaling pathway, or it may be secondary to the failure of septal development.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-1379240, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-1459450, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-1680565, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-3162101, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-3464614, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-7607068, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-7923367, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-7926783, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-7926784, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-7958896, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-8207020, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-8395349, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-849806, http://linkedlifedata.com/resource/pubmed/commentcorrection/7638202-8506363
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
92
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7386-90
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:7638202-Animals, pubmed-meshheading:7638202-Disease Models, Animal, pubmed-meshheading:7638202-Female, pubmed-meshheading:7638202-Heart Atria, pubmed-meshheading:7638202-Heart Conduction System, pubmed-meshheading:7638202-Heart Defects, Congenital, pubmed-meshheading:7638202-Heart Ventricles, pubmed-meshheading:7638202-Homozygote, pubmed-meshheading:7638202-In Situ Hybridization, pubmed-meshheading:7638202-Male, pubmed-meshheading:7638202-Mice, pubmed-meshheading:7638202-Mice, Mutant Strains, pubmed-meshheading:7638202-Microscopy, Video, pubmed-meshheading:7638202-Myocardial Contraction, pubmed-meshheading:7638202-Phenotype, pubmed-meshheading:7638202-Pregnancy, pubmed-meshheading:7638202-RNA Probes, pubmed-meshheading:7638202-Receptors, Retinoic Acid, pubmed-meshheading:7638202-Retinoid X Receptors, pubmed-meshheading:7638202-Transcription Factors, pubmed-meshheading:7638202-Ventricular Function
pubmed:year
1995
pubmed:articleTitle
Atrial-like phenotype is associated with embryonic ventricular failure in retinoid X receptor alpha -/- mice.
pubmed:affiliation
Center for Molecular Genetics, University of California at San Diego, La Jolla 92093, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't