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Authordc.contributor.authorAllen, David D. 
Authordc.contributor.authorCárdenas, Ana María 
Authordc.contributor.authorArriagada, Christian 
Authordc.contributor.authorBennett, Lori B. 
Authordc.contributor.authorGarcía, Carlos J. 
Authordc.contributor.authorCaviedes, Ral 
Authordc.contributor.authorRapoport, Stanley I. 
Authordc.contributor.authorCaviedes, Pablo 
Admission datedc.date.accessioned2019-01-29T17:51:55Z
Available datedc.date.available2019-01-29T17:51:55Z
Publication datedc.date.issued2002
Cita de ítemdc.identifier.citationNeuroReport, Volumen 13, Issue 4, 2018, Pages 491-496
Identifierdc.identifier.issn09594965
Identifierdc.identifier.other10.1097/00001756-200203250-00027
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/163609
Abstractdc.description.abstractWe have established two immortalized cell lines from dorsal root ganglia of normal (G4b) and trisomy 16 mice (GTI), a model for Down syndrome. By immunohistochemistry, both cell lines exhibit neuronal traits and lack glial markers. GTI cells exhibited greater [3H]choline uptake than G4b cells. K+ and nicotine-mediated acetylcholine release was greater in GTI cells. Basal intracellular Ca2+ concentration ([Ca2+]i) was significantly lower in GTI cells. More GTI cells responded to neurotransmitters with a transient [Ca2+]i increase compared to G4b cells, but both cell types showed similar amplitudes of [Ca2+]i responses. The results show that both cell lines retain neuronal characteristics and respond to specific neurotransmitter stimuli. Altered GTI cell responses could be related to neuronal pathophysiology in Down's syndrome. © 2002 Lippincott Williams & Wilkins.
Lenguagedc.language.isoen
Publisherdc.publisherLippincott Williams and Wilkins
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceNeuroReport
Keywordsdc.subjectCalcium signaling
Keywordsdc.subjectCholine uptake
Keywordsdc.subjectDown syndrome
Keywordsdc.subjectMurine trisomy 16
Títulodc.titleA dorsal root ganglia cell line derived from trisomy 16 fetal mice, a model for Down syndrome
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile