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dc.contributor.authorZhang, Jinhua
dc.contributor.authorSmith, Deborah
dc.contributor.authorYamamoto, Miyuki
dc.contributor.authorMa, Lanhua
dc.contributor.authorMcCaffery, Peter J.
dc.date2022-08-11T08:09:31.000
dc.date.accessioned2022-08-23T16:34:19Z
dc.date.available2022-08-23T16:34:19Z
dc.date.issued2003-08-22
dc.date.submitted2009-03-10
dc.identifier.citationJ Neurosci. 2003 Aug 20;23(20):7610-20.
dc.identifier.issn1529-2401 (Electronic)
dc.identifier.pmid12930800
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38303
dc.description.abstractOne general function for retinoic acid (RA) is pattern organization in the CNS. This regulatory factor has an essential role in spinal cord motor neuron and early posterior hindbrain development. In the anterior CNS, however, there is only a limited number of foci of RA synthesis, and less attention has been placed on regions such as the anterior hindbrain where RA synthesizing enzymes are absent. This study shows that a rich source of RA lies around the hindbrain from the RA synthetic enzyme retinaldehyde dehydrogenase-2 (RALDH2) present in the surrounding meninges and mesenchyme by embryonic day 13. RALDH2 is not distributed uniformly throughout the meninges but is restricted to territories over the developing hindbrain, suggesting that RA signaling may be localized to those regions. Further regulation of RA signaling is provided by the presence of a RA sink in the form of the CYP26B1 RA catabolic enzyme expressed in deeper regions of the brain. As a guide to the neural anatomy of hindbrain RA signaling, we used a mouse transgenic for a lacZ reporter gene driven by a RA response element (RAREhsplacZ) to identify regions of RA signaling. This reporter mouse provides evidence that RA signaling in the hindbrain after embryonic day 13 occurs in the regions of the cerebellum and precerebellar system adjacent to sources of RA, including the inferior olive and the pontine nuclei.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=12930800&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAldehyde Oxidoreductases
dc.subjectAnimals
dc.subjectCell Movement
dc.subjectCells, Cultured
dc.subjectCerebellum
dc.subjectCytochrome P-450 Enzyme System
dc.subjectGenes, Reporter
dc.subjectIn Situ Hybridization
dc.subjectMeninges
dc.subjectMice
dc.subjectMice, Transgenic
dc.subjectModels, Neurological
dc.subjectNeurons
dc.subjectRNA, Messenger
dc.subjectReceptors, Retinoic Acid
dc.subjectResponse Elements
dc.subjectRetinal Dehydrogenase
dc.subjectRhombencephalon
dc.subjectTretinoin
dc.subjectbeta-Galactosidase
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleThe meninges is a source of retinoic acid for the late-developing hindbrain
dc.typeJournal Article
dc.source.journaltitleThe Journal of neuroscience : the official journal of the Society for Neuroscience
dc.source.volume23
dc.source.issue20
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2172&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1173
dc.identifier.contextkey770151
refterms.dateFOA2022-08-23T16:34:19Z
html.description.abstract<p>One general function for retinoic acid (RA) is pattern organization in the CNS. This regulatory factor has an essential role in spinal cord motor neuron and early posterior hindbrain development. In the anterior CNS, however, there is only a limited number of foci of RA synthesis, and less attention has been placed on regions such as the anterior hindbrain where RA synthesizing enzymes are absent. This study shows that a rich source of RA lies around the hindbrain from the RA synthetic enzyme retinaldehyde dehydrogenase-2 (RALDH2) present in the surrounding meninges and mesenchyme by embryonic day 13. RALDH2 is not distributed uniformly throughout the meninges but is restricted to territories over the developing hindbrain, suggesting that RA signaling may be localized to those regions. Further regulation of RA signaling is provided by the presence of a RA sink in the form of the CYP26B1 RA catabolic enzyme expressed in deeper regions of the brain. As a guide to the neural anatomy of hindbrain RA signaling, we used a mouse transgenic for a lacZ reporter gene driven by a RA response element (RAREhsplacZ) to identify regions of RA signaling. This reporter mouse provides evidence that RA signaling in the hindbrain after embryonic day 13 occurs in the regions of the cerebellum and precerebellar system adjacent to sources of RA, including the inferior olive and the pontine nuclei.</p>
dc.identifier.submissionpathoapubs/1173
dc.contributor.departmentE. Kennedy Shriver Center
dc.source.pages7610-20


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